Skip to main content
PMC home page
Molecular Systems Biology logoLink to Molecular Systems Biology
. 2015 Apr 16;11(4):799. doi: 10.15252/msb.20145399

Integrative network analysis reveals molecular mechanisms of blood pressure regulation

Tianxiao Huan 1,2,†, Qingying Meng 3, Mohamed A Saleh 4,5, Allison E Norlander 4, Roby Joehanes 1,2,6,7,8,†, Jun Zhu 9,10, Brian H Chen 1,2,†, Bin Zhang 9,10, Andrew D Johnson 1,11,†, Saixia Ying 6,†, Paul Courchesne 1,2,†, Nalini Raghavachari 12,†, Richard Wang 13,†, Poching Liu 13,†; The International Consortium for Blood Pressure GWAS (ICBP), Christopher J O'Donnell 1,11,†, Ramachandran Vasan 1,†, Peter J Munson 6,†, Meena S Madhur 4, David G Harrison 4, Xia Yang 3,✉, Daniel Levy 1,2,†,✉
PMCID: PMC4422556  PMID: 25882670

Abstract

Genome‐wide association studies (GWAS) have identified numerous loci associated with blood pressure (BP). The molecular mechanisms underlying BP regulation, however, remain unclear. We investigated BP‐associated molecular mechanisms by integrating BP GWAS with whole blood mRNA expression profiles in 3,679 individuals, using network approaches. BP transcriptomic signatures at the single‐gene and the coexpression network module levels were identified. Four coexpression modules were identified as potentially causal based on genetic inference because expression‐related SNPs for their corresponding genes demonstrated enrichment for BP GWAS signals. Genes from the four modules were further projected onto predefined molecular interaction networks, revealing key drivers. Gene subnetworks entailing molecular interactions between key drivers and BP‐related genes were uncovered. As proof‐of‐concept, we validated SH2B3, one of the top key drivers, using Sh2b3 −/− mice. We found that a significant number of genes predicted to be regulated by SH2B3 in gene networks are perturbed in Sh2b3 −/− mice, which demonstrate an exaggerated pressor response to angiotensin II infusion. Our findings may help to identify novel targets for the prevention or treatment of hypertension.

Keywords: blood pressure, coexpression network, gene expression, hypertension, systems biology

Subject Categories: Genome-Scale & Integrative Biology, Molecular Biology of Disease

Introduction

Blood pressure (BP) is a highly heritable physiological trait that is regulated through the interactions of numerous genes and environmental factors. Over one billion people worldwide suffer from hypertension (systolic BP [SBP] ≥ 140 mm Hg or diastolic BP [DBP] ≥ 90 mm Hg) (Kearney et al, 2005). BP elevation contributes to nearly half the deaths from cardiovascular disease (CVD) (Lawes et al, 2006; Ehret & Caulfield, 2013). BP control in hypertensive individuals, in turn, is an effective intervention for reducing CVD risk (Lewington et al, 2002). It is hoped that advances from understanding the molecular underpinnings of BP regulation will improve the prediction of CVD susceptibility and offer insights into personalized treatments for hypertension that can reduce the risk of its sequelae.

A recent genome‐wide association study (GWAS) meta‐analysis of up to 200,000 people identified 29 genetic variants (at 28 loci) associated with BP (Ehret et al, 2011). However, the proportion of interindividual BP variability explained by these genetic variants was only about 1% (Ehret et al, 2011). It has been increasingly recognized that genes, instead of working in isolation, interact with other genes in complex regulatory networks, such as gene coexpression networks comprised of modules of genes demonstrating high levels of coregulation (Zhang & Horvath, 2005; Langfelder & Horvath, 2008). Genetic variants associated with diseases can perturb specific parts of gene networks, termed subnetworks, whose overall dysregulation shifts homeostatic processes and leads to disease (Huan et al, 2013; Civelek & Lusis, 2014; Mäkinen et al, 2014). Along the same line, we hypothesized that the top genetic loci identified in BP GWAS, together with a large number of additional genetic variants with more subtle effects, drive shifts in specific gene subnetworks that in turn affect BP.

We designed a systems biology framework to integrate gene expression (in this study, gene expression refers to mRNA expression) profiles with BP GWAS and cellular network models as a means to explore molecular mechanisms influencing BP regulation (Fig 1). We conducted our research using genetic and transcriptomic data (17,318 measured gene transcripts) from 3,679 Framingham Heart Study (FHS) participants who were not receiving antihypertensive drug treatment. At first, we investigated the association of BP with transcriptomic changes at the individual‐gene level by identifying differentially expressed genes for BP transcriptome‐wide (i.e., the top BP signature gene set) and at the multiple‐gene level by identifying BP‐associated coexpression network modules (coEMs). To identify BP coEMs, we first constructed a coexpression network from the gene expression data from all 3,679 samples in order to capture coexpression modules containing highly coregulated genes across all individuals. We then identified BP coEMs whose eigengenes (representing the expression patterns of all genes in each module) demonstrated significant correlations with BP measurements. The advantage of a coexpression network approach is that it provides a contextual framework to determine the relationship between the phenotype and functionally related genes across a population. Second, to differentiate BP‐correlated gene sets that are potentially causal, we linked the top BP signature gene set and the BP coEMs (both representing BP gene sets) with expression‐associated single nucleotide polymorphisms (eSNPs) and with BP GWAS SNPs (Ehret et al, 2011) to identify genetically inferred causal BP gene sets. A BP gene set was considered causal by genetic inference if it was significantly enriched with eSNPs that demonstrated low P‐values in BP GWAS (Ehret et al, 2011). Third, further integration of the observed genetically inferred causal BP gene sets with molecular networks including protein–protein interaction (PPI) networks (Keshava Prasad et al, 2009) and blood Bayesian networks (Emilsson et al, 2008) uncovered key driver (KD) genes that serve as network hubs by interconnecting genes in the genetically inferred causal BP gene sets. Forth, KDs were further ranked by leveraging their associations with BP in GWAS and their differential expression in relation to BP. Lastly, as proof‐of‐concept, we investigated the role of one of the top KDs, SH2B3, in relation to hypertension using a Sh2b3 −/− mouse model, and tested the genes in the predicted SH2B3 subnetworks for enrichment with differentially expressed genes in the knockout mouse model.

Figure 1. The integrative network‐based approach for identifying and prioritizing key drivers of blood pressure regulation.

Figure 1

Open in a new tab

This figure depicts the analysis framework. First, identify blood pressure (BP)‐associated transcriptomic changes in individual‐gene level by identifying differentially expressed signature genes, and in multiple‐gene level by identifying BP‐associated coexpression network modules (BP coEMs). Second, integrate both the BP top signatures gene set and the BP coEMs, with BP genome‐wide association studies (GWAS) results as well as eSNPs by the SNP set enrichment method (SSEA) (Zhong et al, 2010) to identify genetically inferred causal BP gene sets. Third, project the genes of the genetically inferred causal BP gene sets onto network models to prioritize and identify key driver (KD) genes. Finally, identify BP‐associated subnetworks derived by top KDs. ICBP = International Consortium for Blood Pressure, PPI = protein–protein interaction.

Results

Clinical characteristics of study participants

The FHS recently launched the Systems Approach to Biomarker Research in Cardiovascular Disease (SABRe CVD) initiative, which seeks to explore and characterize biomarkers and molecular underpinnings of CVD and its risk factors, including BP. High‐throughput gene expression profiles from whole‐blood‐derived RNA were generated in 5,626 individuals of European ancestry from the FHS offspring (n = 2,446) and the third‐generation (n = 3,180) cohorts. In order to avoid the confounding effects of drug treatment on gene expression levels, this study was restricted to 3,679 participants who were not receiving antihypertensive treatment.

The clinical characteristics of the 3,679 study participants are summarized in Table 1. The mean age of study samples was 51 years (range 24–92) and 58% were female. The distribution of systolic (SBP) and diastolic BP (DBP) is shown in Supplementary Fig S1. The average SBP/DBP was 118/74 mm Hg, and 11% of participants had hypertension (HTN; defined as SBP ≥ 140 mm Hg or DBP ≥ 90 mm Hg). Pre‐hypertension, defined as a SBP from 120 to 139 mm Hg or DBP from 80 to 89 mm Hg, was present in 17% of our participants.

Table 1.

Clinical characteristics of FHS participants

Phenotypes/Covariates Offspring cohort N = 1,102 (examination cycle 8: 2005–2008)a Third‐generation cohort N = 2,577 (examination cycle 2: 2008–2011)a
Mean ± SD Mean ± SD
Male (%) 38 44
Age (years) 63 ± 9 45 ± 8
Body mass index (kg/m2) 27.1 ± 5.0 27.2 ± 5.4
Systolic BP (mm Hg) 126 ± 16 115 ± 14
Diastolic BP (mm Hg) 75 ± 10 74 ± 9
Hypertension (%) 21 7
Open in a new tab
a

Individuals who were receiving antihypertensive treatment were excluded in this study.

Influence of blood cell types on BP‐associated gene expression differences

As mRNA expression levels might be influenced by differences in the proportions of different cell types in whole blood, we assessed the correlations between mRNAs and three major cell‐type proportions. We found that approximately 42% of genes were significantly correlated with cell‐type proportions at Bonferroni‐corrected P < 0.05 (Supplementary Table S1), suggesting a major impact of blood cell types on gene expression. As results from both cell type‐adjusted and cell type‐unadjusted analyses could be biologically relevant (the adjusted analysis may reflect cell‐type‐independent signals and the unadjusted analysis may represent cell‐type‐dependent signals), we report both sets of results but focus our discussions on the adjusted analysis to simplify results interpretation. We also report the similarities and differences between the two analyses.

Identification of transcriptome‐wide gene expression signatures for BP

To characterize significant transcriptomic changes at the single‐gene level, we correlated each gene with BP phenotypes (SBP, DBP, and HTN) after accounting for age, sex, body mass index (BMI), cell types, technical covariates, and familial relatedness (detailed in the Materials and Methods section). Eighty‐three genes whose expression levels were correlated with BP (73 for SBP, 31 for DBP, and eight for HTN) were identified at Bonferroni‐corrected P < 0.05 (corrected for 17,318 measured genes) (Supplementary Dataset S1). These 83 signature genes are referred to as the BP signature gene set. Among the 83 genes, 65 were positively correlated with BP traits and eight were negatively correlated. Five genes, TSPAN2, GZMB, MYADM, ANXA1, and FAR2, were correlated with SBP, DBP, and HTN. A total of 66 BP‐correlated genes were identified from the analysis that did not adjust for cell types (Supplementary Dataset S2). Fifty‐five genes (66%) identified in the adjusted analysis overlapped with those from the unadjusted analysis.

Construction of coexpression networks and identification of BP‐associated gene coexpression modules

To characterize BP‐associated transcriptomic changes at a global level, we investigated coexpression patterns of multiple genes. We first constructed gene coexpression networks from gene expression data after adjusting for age, sex, BMI, cell types, technical covariates, and cohort to identify gene coexpression network modules (coEMs). Subsequently, we correlated the coEMs with BP values to capture the genomic coregulatory structure associated with BP variability. We identified 27 coEMs (Fig 2A; Supplementary Fig S2; the names of the coEMs are represented by different colors). Six coEMs (Turquoise, Blue, Red, Purple, Lightyellow, and Chocolate modules) were associated with either SBP or DBP at P < 0.05 and passed FDR < 0.2 (Fig 2B; Supplementary Fig S3). The Chocolate module passed FDR < 0.05. The Chocolate and Red modules were significantly enriched for genes in the BP signature gene set (P‐values are 6.3e‐12 and 0.03, respectively; Fig 2C).

Figure 2. Identification of BP‐associated coexpression network modules (coEMs).

Figure 2

Open in a new tab
  1. The topological overlap matrix (TOM) plot of coexpression network identified from gene expression profiling in 3,679 FHS participants. The six BP coEMs were highlighted.
  2. The associations of eigengenes of each BP coEM with BP phenotypes (SBP or DBP). The y‐axis is −log10‐transformed P‐value for the minimum association between the eigengenes of the module and BP traits (systolic or diastolic BP).
  3. The enrichment of BP top signature genes in each BP coEM. The y‐axis is –log10‐transformed the enrichment P‐value.

We also constructed coexpression networks using the data that were unadjusted for cell types (Supplementary Fig S2). We identified 32 coEMs, of which the eigengenes of seven coEMs (Green, Greenyellow, Cyan, Magenta, Tan, Midnigtblue, and Lightgreen modules) showed significant correlation with SBP or DBP at P < 0.05. The Purple and Chocolate coEMs from the cell type‐adjusted network were conserved with the Green and Lightgreen coEMs from the cell type‐unadjusted results, respectively. The Turquoise coEM from the adjusted analysis split to three modules in the unadjusted analysis. Other coEMs were unique to the adjusted or unadjusted analysis (Supplementary Fig S4).

Gene ontology (GO) enrichment analysis

To understand the biological pathways and functional categories of the BP transcriptomic changes, we conducted GO enrichment analysis of the BP signature gene set and the BP‐correlated coEMs identified above. GO enrichment analysis for the BP signature gene set and coEMs from the cell type‐adjusted analysis showed that the 83‐gene BP signature gene set did not show any significantly enriched GO terms at Bonferroni‐corrected P < 0.05. The top suggestive GO term enriched in the 83‐gene signature set was apoptotic process (P = 1.4e‐3). The Turquoise coEM is enriched with genes involved in chromatin modification (Bonferroni‐corrected [BF] P = 3.8e‐14), intracellular transport (BF P = 1.1e‐11), and regulation of gene expression (BF P = 5.9e‐11). The Purple coEM was enriched for hemostasis (BF P = 5.0e‐4), platelet activation (BF P = 1.8e‐3), and wound healing (BF P = 7.5e‐3). The Chocolate coEM was enriched for immune cell‐mediated cytotoxicity (BF P = 2.6e‐8), cellular defense response (BF P = 3.9e‐6), and inflammatory response (BF P = 1.3e‐5) (Table 2). These results suggest that genes involved in multiple biological processes are tightly coregulated in relation to BP.

Table 2.

Gene ontology enrichment analysis of the BP coexpression modules

Gene set Biological process terms Gene count Fold change P‐value Bonferroni‐corrected P
Turquoise Chromatin modification 89 2.5 4.6e‐17 3.8e‐14
Intracellular transport 156 1.8 1.3e‐14 1.1e‐11
Regulation of gene expression 382 1.4 7.1e‐14 5.9e‐11
Purple Hemostasis 14 5.1 6.1e‐7 5.0e‐4
Platelet activation 9 7.8 2.2e‐6 1.8e‐3
Wound healing 14 4.1 9.1e‐6 7.5e‐3
Chocolate Immune cell‐mediated cytotoxicity 7 54.9 3.1e‐11 2.6e‐8
Cellular defense response 10 12.4 4.7e‐9 3.9e‐6
Inflammatory response 14 6.3 1.6e‐8 1.3e‐5
Open in a new tab

GO enrichment analysis for the coEMs from the cell type‐unadjusted analysis showed significant enrichment of similar sets for biological processes or pathways as revealed by the coEMs in the adjusted analysis (Supplementary Table S2), suggesting that most of the BP coEMs and their represented biological process/pathways were relatively stable and were not affected by adjustment for cell counts.

Inferring causal modules using SNP set enrichment analysis (SSEA)

The BP signature genes and coEMs identified above could either play a causal role in regulating BP or be reactive to or independent of BP change. To differentiate these relationships, we used SSEA to evaluate whether the BP gene sets demonstrated enrichment for BP GWAS signals. For each BP‐correlated gene set, we first retrieved blood eSNPs that showed association with the blood expression levels of genes in each BP‐correlated gene set, and then extracted the BP association P‐values of the eSNPs in the ICBP GWAS. Lastly, the overall distribution of the BP association P‐values of the eSNPs representing each BP gene set was compared to the null distribution of all blood eSNPs using two statistical tests, the Kolmogorov–Smirnov (KS) test and Fisher's exact test, to test whether the given BP gene set showed significant overall enrichment for eSNPs with stronger BP associations (see the Materials and Methods section). A BP gene set showing significance in SSEA is referred to as ‘genetically inferred causal’, because it is supported by orthogonal genetic evidence (i.e., association of its eSNPs with BP in GWAS) that is unlikely to be confounded by nongenetic factors. The same term also implies that further experimental validation is needed to establish causality with certainty.

Four coEMs from the cell count‐adjusted network (Turquoise, Blue, Red, and Chocolate coEMs) were identified as genetically inferred causal gene sets at Bonferroni‐corrected P < 0.05 by both KS and Fisher's exact tests (Table 3). The BP signature gene set, however, did not show enrichment for BP GWAS eSNPs. To explore which top genes contributed to the overall enrichment for BP‐related genetic variants in the four genetically inferred causal coEMs, we retrieved the ICBP GWAS P‐values for the blood eSNPs within these gene sets. We found that the blood eSNPs of 15 genes in the genetically inferred causal coEMs reached P < 5e‐8 in the ICBP BP GWAS (Ehret et al, 2011) (Table 4). For example, rs3184504 (associated with BP in GWAS) is located in the third exon of SH2B3 and is associated with the expression of four genes in the genetically inferred causal BP gene sets, including three genes (SH2B3, ALDH2, and NAA25) in cis and two genes (IL8 and TAGAP) in trans. In addition, there are 34 additional genes whose cis‐ or trans‐eSNPs (390 eSNPs in total) are associated with BP in the ICBP BP GWAS (Ehret et al, 2011) at P < 1e‐5 (Supplementary Dataset S3). The SSEA results indicate that many genes in these genetically inferred causal BP gene sets carry a number of eSNPs (from whole blood profiling) with strong or moderate effects on BP regulation.

Table 3.

SNP set enrichment analysis of BP coexpression modules and BP signature gene set

Module SBP GWAS DBP GWAS
KS P Permutation‐based KS P a Fisher P Permutation‐based Fisher P a KS P Permutation‐based KS P Fisher P Permutation‐based Fisher P a
BP signature 0.98 0.96 1 1 0.20 0.23 1 1
Turquoise 2.8e‐45 < 0.001 7.8e‐115 < 0.001 1.8e‐28 < 0.001 3.0e‐39 < 0.001
Blue 1.4e‐44 < 0.001 7.0e‐54 < 0.001 1.3e‐8 < 0.001 3.4e‐15 < 0.001
Red 8.0e‐5 < 0.001 1.7e‐17 < 0.001 2.2e‐15 < 0.001 6.7e‐19 < 0.001
Purple 0.65 0.71 0.58 0.61 1 1 1 1
Lightyellow 1.6e‐3 0.004 1 1 0.12 0.16 1 1
Chocolate 2.3e‐14 < 0.001 5.0e‐5 < 0.001 0.07 0.06 1 1
Open in a new tab
a

Permutation‐based P is empirically derived based on 1,000 permutations (see Materials and Methods). < 0.001 indicates none of the 1,000 random gene sets of matching size had P‐values lower than the observed test P‐values.

Table 4.

Genes in the genetically inferred causal BP gene sets whose blood eSNPs show significant association with BP in GWAS at P < 5e‐8

SNP (Genomic location) SNP Chr ICBP GWAS SBP P‐value ICBP GWAS DBP P‐value cis or trans Gene symbol Gene chr Gene set
rs3184504 (Coding, SH2B3)a chr12 9.3e‐10 2.3e‐14 cis ALDH2 chr12 Turquoise
SH2B3 chr12 Turquoise
NAA25 chr12 Blue
trans b IL8 chr4 Turquoise
TAGAP chr6 Blue
rs3742004 (3UTR, FAM109A) chr12 1.0e‐6 2.2e‐8 cis ATXN2 chr12 Turquoise
rs17367504 (Intron, MTHFR) chr1 2.1e‐10 1.3e‐8 cis CLCN6 chr1 Turquoise
rs17249754 (Coding, ATP2B1) chr12 9.7e‐13 5.3e‐9 cis GALNT4 chr12 Blue
rs198846 (3downstream, HIST1H1T) chr6 2.2e‐5 3.8e‐8 cis HIST1H4B chr6 Turquoise
BTN3A2 chr6 Turquoise
HIST1H4C chr6 Turquoise
HIST1H2BF chr6 Turquoise
HIST1H4F chr6 Turquoise
HIST1H3B chr6 Blue
rs17115100 (Intron, CYP17A1) chr10 9.2e‐10 1.4e‐5 cis SFXN2 chr10 Blue
Open in a new tab
a

A proxy SNP rs653178 (r 2 = 1 with rs3184504) showing same cis‐ and trans‐associations with genes listed for rs3184504. rs653178 is significantly associated with both SBP and DBP in ICBP GWAS, too (SBP P = 9.3e‐10, and DBP P = 1.6e‐14).

b

The trans‐associations between rs3184504 and those genes identified from Westra et al (2013).

We also performed SSEA on the BP coEMs identified in the gene expression data without adjusting for cell types (Supplementary Table S3). The corresponding coEMs from the unadjusted analysis that significantly overlap with the Turquoise and Chocolate coEMs from the cell type‐adjusted analysis remained significant in the SSEA analysis. Two other coEMs unique to the unadjusted analysis were found to be additional signals demonstrating enrichment for BP eSNPs (Supplementary Table S3).

Identification of key drivers (KDs)

Recent studies have shown that disease genes (or functionally correlated genes) are not distributed randomly in cellular or molecular interaction networks (Goh et al, 2007). Therefore, the graphic structure of the corresponding network models may help prioritize candidate genes for disease (Barabási et al, 2011; Huan et al, 2013; Zhang et al, 2013; Mäkinen et al, 2014). Based on this assumption, we took advantage of pre‐compiled blood Bayesian networks (BNs) (Emilsson et al, 2008) and protein–protein interaction (PPI) networks (Keshava Prasad et al, 2009) to identify key drivers (KDs) of the genetically inferred causal BP gene sets identified by SSEA. A KD is referred to as a local network hub whose neighbors in its local subnetwork show enrichment for BP genes in the genetically inferred causal gene sets. Due to their central location in the networks, KDs may have broad impact on multiple genes related to BP.

We projected the genes from each of the four genetically inferred causal BP coEMs constructed form cell count‐adjusted results onto the blood BNs and the PPI network, and identified KDs using a KD analysis (Huan et al, 2013; Zhang et al, 2013), as detailed in the Materials and Methods section. Briefly, we took each gene in a given network as a candidate KD and tested whether the network neighborhood of the candidate KD was enriched for gene members of the genetically inferred causal BP gene set using Fisher's exact test. At Bonferroni‐corrected P < 0.05, we identified 545 KDs from the HPRD PPI network (Keshava Prasad et al, 2009) and 131 from the blood BN (Supplementary Dataset S4). We further tested the reliability of these PPI KDs using an independent PPI database, BioGrid (Chatr‐Aryamontri et al, 2013). We found that even though the direct overlap in PPIs between the two PPI databases was limited (15%), a considerably larger proportion of KDs replicated: 36% of KDs identified in HPRD replicated in BioGrid for the four genetically inferred causal BP coEMs, and 50% of KDs in the Turquoise module replicated.

KDs were further ranked by leveraging their associations in BP GWAS, BP correlations, and their statistical significance in the KD analysis (see the Materials and Methods section). Table 5 lists the top 20 KDs, including seven genes having eSNPs associated with BP at P < 1e‐5 in the ICBP BP GWAS (Ehret et al, 2011), 11 genes showing differential expression in relation to BP at transcriptome‐wide significance, and two top KDs identified from both PPI and blood BNs.

Table 5.

Top key drivers (KDs)

KD Cellular network TWAS GWAS
KD P‐value, corrected for subnetwork size Tissue / network P‐valuea for BP TWAS eSNP ID P‐valueb in ICBP GWAS BP coEM
Top BP GWAS KDs
 SH2B3 4.4e‐4 HPRD rs653178 1.6e‐14 Turquoise
 ATXN2 c 2.2e‐5 HPRD rs3742004 2.2e‐8 Turquoise
 NMT1 1.6e‐5 HPRD rs12946454 8.9e‐8 Turquoise
 NSF 5.0e‐9 HPRD rs17608766 7.3e‐7 Turquoise
 HSPA1B 2.1e‐9 HPRD rs805303 1.3e‐6 Blue
 BAT2 5.4e‐7 HPRD rs805303d 1.3e‐6 Turquoise
 MAPKAPK5 c 2.8e‐8 HPRD rs4767293 1.5e‐6 Turquoise
Top BP TWAS KDs
 GZMB c 2.0e‐23 Blood 4.8e‐22 Chocolate
 PRF1 2.0e‐26 Blood 2.5e‐9 Chocolate
 GPR56 1.2e‐26 Blood 3.5e‐9 Chocolate
 RAB11FIP1 1.3e‐3 Blood 4.0e‐8 Turquoise
 HIPK1 c 3.1e‐8 HPRD 9.1e‐8 Turquoise
 GZMH c 5.4e‐24 Blood 3.3e‐7 Chocolate
 VIM 6.0e‐3 HPRD 4.2e‐7 Turquoise
 BCL2L11 c 1.8e‐10 HPRD 1.7e‐6 Blue
 BHLHE40 c 3.8e‐7 HPRD 2.2e‐6 Turquoise
 KLRD1 1.2e‐30 Blood 2.5e‐6 Chocolate
 TGFBR3 1.1e‐26 Blood 2.5e‐6 Chocolate
Top multi‐tissue/ network KDs
 DCLRE1C c 1.1e‐16 HPRD, Blood Blue
 ERCC6 8.8e‐14 HPRD, Blood Turquoise
Open in a new tab
a

P‐values passing transcriptome‐wide significance at Bonferroni‐corrected P < 0.05 (corrected for 17,318 measured genes).

b

Minimum P‐values for SBP, DBP, and HTN associations.

c

Indicating the KD could be replicated in BioGrid PPI database (Chatr‐Aryamontri et al, 2013).

d

trans‐eSNP; other eSNPs are cis‐eSNPs.

PPI, protein–protein interaction; HPRD, Human Protein Reference Database (Keshava Prasad et al, 2009).

Inferring BP gene regulatory subnetworks driven by top key drivers

We retrieved subnetworks derived from the top KDs in the blood BNs (Emilsson et al, 2008) and the HPRD PPI network (three examples are shown in Supplementary Fig S5). In Fig 3, we show subnetworks related to a top KD SH2B3 as a proof‐of‐concept. A missense SNP (rs3184504) located in an exon of SH2B3 (Fig 3A) was associated with BP and hypertension in GWAS (Ehret et al, 2011). rs3184504 has also been reported as a cis‐eSNP for three genes and a trans‐eSNP for sixteen genes in previous eSNP studies (Westra et al, 2013) (Joehanes et al, 2013a,b). Among all the candidate genes for BP identified in this study, we found 10 whose expression changes were associated with rs3184504 (two in cis and eight in trans), which constitute the ‘SH2B3 genetic subnetwork’ (Fig 3B). The 10 genes are as follows: SH2B3 (cis), a top BP KD; ALDH2 (cis), TAGAP (trans), and IL8 (trans), which are in the genetically inferred causal BP coEM (turquoise); ARHGEF40 (trans), TAGAP (trans), MYADM (trans), FOS (trans), PPP1R15A (trans), and S100A10 (trans), which are in the top BP signature gene set (green). The SH2B3‐derived PPI subnetwork (Fig 3C) is enriched for genes involved in intracellular signaling cascade (P = 1.2e‐24), T‐cell activation (P = 4.1e‐12), and T‐cell differentiation (P = 1.4e‐9). This SH2B3 subnetwork included STAT1, which is trans‐associated with rs3184504, and two top BP signature genes KCNJ2 and PTPRO.

Figure 3. SH2B3‐related genetic and protein–protein interaction subnetworks.

Figure 3

Open in a new tab
  1. rs3184504, a missense SNP, is located in the third exon of SH2B3.
  2. SH2B3 genetic subnetwork. rs3184504 is associated with 19 genes in a cis or trans manner based on analysis of eQTLs.
  3. SH2B3 protein–protein interaction (PPI) subnetwork. SH2B3 is depicted as a rectangular node. Green nodes indicate differentially expressed BP genes at Bonferroni‐corrected P < 0.05 in the Framingham Heart Study (FHS) data (BP Top Sig); turquoise nodes indicate genes in the BP causal coEMs; yellow nodes indicate genes that are in both the BP Top Sig set and the BP causal coEMs. The nodes marked with a red border indicate differentially expressed genes between wild‐type (WT) and Sh2b3 −/− mice.

In order to systematically check whether the SH2B3‐derived PPI subnetwork showed any enrichment for literature‐based BP‐related genes, we created a list of 657 BP‐related genes by searching GeneRif (http://www.ncbi.nlm.nih.gov/gene/about-generif; downloaded in Jan 2015) using the keywords ‘hypertension’ and ‘blood pressure’. GeneRif includes literature descriptions of 14,069 unique human genes in total. We found that 41 of the 657 genes were present in the SH2B3‐derived PPI subnetwork, which consisted of 362 genes in total, including PLCE1 (Ehret et al, 2011), BAT2 (Ehret et al, 2011), ADRB2 (Lou et al, 2010), RHOA (Connolly & Aaronson, 2011), and SOCS1 (Satou et al, 2012). Comparison of the two ratios 656/14,069 and 41/362 yielded P = 5.5e‐8 (by the hypergeometric test) and 2.43‐fold enrichment. This result indicates that the SH2B3‐derived PPI subnetwork is enriched for known BP‐related genes.

Validation of the SH2B3 subnetworks in a Sh2b3 −/− mouse model

Although prior GWAS identified SH2B3 as a positional candidate gene, the role of SH2B3 in BP regulation remains unclear. As stated above, we identified SH2B3 as a putative KD for BP, and subnetworks based on SH2B3 revealed molecular interactions between this KD and many genes and multiple pathways related to BP regulation. In a related study (Saleh et al, 2015), we found that Sh2b3 −/− mice had normal baseline BP but markedly elevated blood pressure in response to a low dose of angiotensin II (Ang II; 140 ng/kg/min) that did not affect BP in wild‐type (WT) mice. This suggests a key role of Sh2b3 in BP regulation, and that loss or changes to this gene exacerbate response to hypertensive stimuli.

To determine the accuracy of the predicted network structure, we performed RNA sequencing of the entire transcriptome in whole blood from WT and Sh2b3 −/− mice. Whole blood was chosen to complement our network finding in whole blood from humans. As shown in Supplementary Fig S6, the RNA reads of exons 3–8 of Sh2b3 in the Sh2b3 −/− mice were absent, in complete agreement with the design of the targeting construct used to produce these mice (Takaki et al, 2000). At a false discovery rate (FDR was estimated using the q value approach) < 0.05, we found 2,240 differentially expressed genes between WT and Sh2b3 −/− mice (Supplementary Dataset S5), supporting a large‐scale perturbation of the transcriptome in the Sh2b3 −/− mice. The gene signatures showed significant enrichment for genes involved in immune response (P = 4.0e‐22), inflammatory response (P = 3.5e‐20), and T‐cell activation (P = 4.1e‐6), consistent with the pathways in the predicted SH2B3 subnetworks. More importantly, as shown in Table 6, these signature genes significantly overlapped with those in the SH2B3 genetic subnetwork (Fig 3B) at P = 1.2e‐5 and the SH2B3 PPI subnetwork (Fig 3C) at P = 2.2e‐14. The overlapping genes between the SH2B3 subnetworks and the signatures observed in Sh2b3 −/− mice (Supplementary Table S4) again showed significant enrichment for intracellular signaling cascade (P = 9.4e‐16) and T‐cell activation (P = 5.0e‐6). These results strongly support our predicted SH2B3 subnetworks. Consistent with our prediction, Saleh et al (2015) also confirmed the exacerbation of inflammation and T‐cell activation in Sh2b3 −/− mice.

Table 6.

Summary of the overlap between gene signatures of Sh2b3 −/− mice and the predicted SH2B3 subnetworks

SH2B3 subnetwork Number of genes in the subnetwork Number of overlapping genes Fold enrichment P‐value
Genetic subnetwork 19 8 2.5 1.2e‐5
PPI subnetwork 362 78 1.3 2.2e‐14
Open in a new tab

Discussion

This study represents a large, single‐site transcriptome‐wide analysis of BP in 3,679 individuals who were not receiving antihypertensive drug treatment. Extending traditional transcriptome‐wide analysis that targets differentially expressed genes at the individual‐gene level, we also conducted higher level coexpression network analysis to identify multiple genes demonstrating coregulatory network structure in the form of coEMs associated with BP. To differentiate causal from reactive roles of the BP‐related genes/gene sets from transcriptome‐wide analysis, we integrated the differentially expressed genes and the BP coEMs with SNP association results from BP GWAS. To further pinpoint key BP genes and dissect key regulatory mechanisms among the genetically inferred causal BP gene sets, we projected genes within these gene sets onto gene/protein networks and identified key drivers (KDs). These KDs appear to regulate a large number of interacting genes in gene subnetworks and orchestrate multiple biological processes and pathways underlying BP regulation.

By first applying a traditional approach that focused on differentially expressed individual genes, we identified a gene signature set comprised of 83 genes whose expression levels were correlated with BP traits. The 83‐gene BP signature gene set did not show significant enrichment for biological processes or pathways suggesting that the traditional single‐gene approach lacks power to capture high‐order organization of genes underlying BP regulation. Subsequent SNP set enrichment analysis (SSEA), which incorporates genetic signals, did not support an overall causal role of the top BP signature genes. Although this lack of overall significance in SSEA does not exclude a small subset of genes being causal, for example, a top signature gene ATP2B1 has been previously detected as a GWAS signal in ICBP GWAS at P < 5 × 10−8. ATP2B1 (ATPase, Ca2+ transporting, plasma membrane 1) is known to be responsible for Ca2+ transportation in plasma membrane, and a BP‐associated ATP2B1 SNP has been linked to ATP2B1 expression in umbilical artery smooth muscle cells (Tabara et al, 2010). Ca2+ is critical for muscle contraction (Marks, 2003), and defects or altered expression of ATP2B1 will likely induce changes in artery smooth muscle contraction which may in turn affect blood pressure variability. Another top signature gene, FOS (known as c‐fos), has been found to be associated with hypertension (Minson et al, 1996; Cunningham et al, 2006). The c‐fos gene is considered to be a useful marker of neuronal activity in different sites, including those important in BP control. In the rat, c‐fos expression in the brain is likely to be important for BP control, and the blockade of c‐fos expression in this region attenuates resting and stimulated BP levels. Inhibition of local neuronal activity acutely increased both BP and immunoreactivity to Fos, the protein product of the c‐fos gene. Intravenous infusion of sodium nitroprusside induced hypotension, and the number of Fos‐positive spinal sympathetic neurons increased (Minson et al, 1996). Several additional BP signature genes have been reported to be involved in BP‐related diseases or processes such as cardiovascular disease (e.g., ABCA1 (Tang & Oram, 2009), AHR (Zhang, 2011), and GZMB (Joehanes et al, 2013a,b)), type II diabetes (e.g., ABCA1 (Tang & Oram, 2009), ANXA1 (Lindgren et al, 2001), and PTGS2 (Shanmugam et al, 2006)), and inflammation (e.g., GZMB (Hiebert & Granville, 2012) and KLRD1 (Choi et al, 2012)). We speculate that these genes may play important roles in BP regulation, but further mechanistic studies are necessary.

To overcome the inherent limitations of single‐gene‐based analysis, we used a coexpression network approach to capture high‐order gene–gene interrelation in association with BP that cannot be revealed by single‐gene‐based analysis. We chose to use WGCNA (Zhang & Horvath, 2005; Langfelder & Horvath, 2008) to construct a gene coexpression network; this approach has revealed patterns associated with other diseases (Chen et al, 2008; Emilsson et al, 2008; Huan et al, 2013; Zhang et al, 2013). The superior performance of WGCNA in detecting biologically coherent gene coregulation structures is built upon its underlying algorithm that takes into consideration not only pairwise gene–gene correlations but also the similarity between a given pair of genes in their correlation structure with the rest of the genome. Incorporation of the higher order relationships in WGCNA yields more coherent coexpression modules compared to classic clustering approaches. Indeed, a majority of the WGCNA modules identified in our study contain functionally related genes. For instance, the Turquoise module is highly enriched for genes involved in transcriptional regulation and chromatin modification; the Chocolate module mainly contains genes important for inflammation and immune response.

Of note, the known functional information was not inputted into network construction; instead, the network modules were purely defined by our blood transcriptome data. The coherence between the coexpression patterns and functional relatedness of the module genes supports the power and accuracy of WGCNA. Further, four of the six modules correlated with BP tested as being causal by genetic inference from SSEA. This is in contrast to the lack of SSEA significance for the BP signature gene set and highlights the capacity of WGCNA to unravel genes and processes that are more likely upstream of BP variation. Moreover, there exists literature support for the biological plausibility of the genetically inferred causal modules detected. For instance, both the Chocolate and Turquoise modules were found to be causally linked to BP regulation. The causal links between immune/inflammatory response represented by the Chocolate module and hypertension have been shown in numerous studies (Harrison et al, 2010, 2011, 2012; Barhoumi et al, 2011). The epigenetic and transcriptional regulations, represented by the Turquoise module, are key processes implicated for many diseases (Maunakea et al, 2010). Recent literature supports the notion that key hypertension genes and pathways, such as the Na+‐K+‐2Cl−‐cotransporter 1 (NKCC1) (Cho et al, 2012) and angiotensin‐converting enzyme 1 (ACE1) (Lee et al, 2012), are epigenetically regulated in relation to hypertension. These lines of evidence support the successful application of coexpression network approaches in this study.

The genetically inferred causal coEMs identified for BP through our network analysis contain a large number of genes that are tightly coregulated, which creates a challenge in finding the ‘key’ regulatory genes and dissecting gene–gene interactions that might provide insight into clinical treatment of hypertension. To address this limitation, we employed graphical molecular networks including Bayesian networks constructed from blood‐derived transcriptomic data (Emilsson et al, 2008) and PPI networks (Keshava Prasad et al, 2009; Chatr‐Aryamontri et al, 2013) that provide detailed topological information regarding gene–gene and protein–protein relations to tease out regulatory cascades and prioritize key regulatory genes for BP. We used a network‐based gene ranking method, key driver (KD) analysis approach, to identify key drivers in each genetically inferred causal coEM. Previous studies have shown that KD analysis has the capacity to uncover novel genes that play important roles in disease development but are missed by traditional approaches (Wang et al, 2012; Huan et al, 2013; Zhang et al, 2013; Mäkinen et al, 2014). Many of the KDs that we identified have previously been reported to be involved in BP regulation, including WNK1 (Choate et al, 2003), BMPR2 (Atkinson et al, 2002; Hamid et al, 2009), GPX1 (Ardanaz et al, 2010), TAF1 (Koschinsky et al, 2001), GYS1 (Groop et al, 1993; Orho‐Melander et al, 1999), CAST (Kokubo et al, 2006), IKBKAP (Kokubo et al, 2006), MEF2A (Oishi et al, 2010), and PPARA (Bernal‐Mizrachi et al, 2003, 2007), supporting the validity of our methods. However, as KDA relies on precomputed gene–gene interaction networks and topology‐based gene ranking, its performance is highly dependent on the quality of the molecular networks used. In particular, the currently available human PPI networks are prone to high false positives (Cusick et al, 2005). Therefore, additional prioritization based on orthogonal evidence and explicit experimental validation is warranted. By implementing multiple criteria to rank KDs, we were able to focus on a subset of KDs that are more likely to be true signals, one of which is SH2B3.

SH2B3 was identified as a top KD (P = 4.4e‐4) in the PPI network (Keshava Prasad et al, 2009). A missense SNP (rs3184504) located in the third exon of SH2B3 was reported to be associated with BP and hypertension in prior GWAS (Ehret et al, 2011). However, the molecular mechanisms relating SH2B3 to BP regulation have not previously been reported. Our network analysis predicted that the SH2B3‐related PPI subnetwork is highly enriched for genes involved in intracellular signaling and T‐cell activation and differentiation. Through transcriptome‐wide sequencing of whole‐blood‐derived RNA from WT and Sh2b3 −/− mice, we found that our predicted SH2B3‐derived genetic and PPI subnetworks overlapped greatly with the differentially expressed genes in Sh2b3 −/− versus WT mice, thus validating our predicted networks derived from humans. In our related paper (Saleh et al, 2015), we confirmed that deletion of Sh2b3 exacerbates Ang II‐induced hypertension via mechanisms involving inflammation and T‐cell activation. These results are consistent with previous evidence linking SH2B3 to a range of signaling cascade activities such as cytokine signaling (Takizawa et al, 2008) as well as recent findings on the role of T lymphocytes in hypertension through a feed‐forward mechanism: modest degrees of blood pressure elevation lead to T‐cell activation, which in turn promotes inflammation and further blood pressure elevation (Marvar et al, 2010; Kirabo et al, 2014). Mice lacking T lymphocytes are resistant to the development of both Ang II‐ and DOCA‐salt‐induced hypertension (Guzik et al, 2007). Our findings therefore demonstrate the utility of our systems biology approach to identify not only candidate genes such as SH2B3 but also gene network‐level mechanism through which the adaptor protein SH2B3 contributes to hypertension through perturbation of inflammatory and T‐cell functions.

In conclusion, our integrative and systems biology analysis, which leveraged transcriptional profiling, GWAS, and network modeling, revealed multiple biological processes that contribute to BP regulation. This approach highlighted putative regulatory roles of key driver genes, most notably SH2B3. The key drivers and the biological processes they regulate form coherent gene–gene regulatory networks. Future follow‐up studies focusing on the novel KDs and their network structures are warranted to provide insights into the complex mechanisms underlying BP pathophysiology.

Materials and Methods

Study participants

Biosamples were collected, and BP measurements were obtained from all available Framingham Heart Study (FHS) offspring cohort participants who attended their eighth clinic examination (2005–2008; n = 2,446) (Feinleib et al, 1975) and third‐generation cohort participants who attended their second examination (2008–2011; n = 31,80) (Splansky et al, 2007). Data from 3,679 participants (offspring cohort, n = 1,102; third‐generation cohort, n = 2,577) who were not receiving antihypertensive drugs were used for this project. Hypertension (HTN) was defined as SBP ≥ 140 mm Hg or DBP ≥ 90 mm Hg. This study followed the recommendations of the Declaration of Helsinki and the Department of Health and Human Services Belmont Report, and is approved under the Boston University Medical Center's protocol H‐27984. Informed consent was obtained from each participant.

Gene expression profiling measurement

Whole blood samples (2.5 ml) were collected in PAXgene™ tubes (PreAnalytiX, Hombrechtikon, Switzerland) during Framingham offspring cohort examination 8 (2005–2008) and during Framingham third‐generation cohort examination 2 (2008–2011). Total RNA was isolated from frozen PAXgene blood tubes by Asuragen, Inc., according to the company's standard operating procedures. The purity and quantity of total RNA samples were determined by absorbance readings at 260 and 280 nm using a NanoDrop ND‐1000 UV spectrophotometer. Expression profiling was carried out on samples that passed RNA quality control. RNA expression was conducted using the Affymetrix Human Exon Array ST 1.0 (Affymetrix, Inc., Santa Clara, CA). All data used herein are available online in dbGaP (http://www.ncbi.nlm.nih.gov/gap; accession number phs000007).

Gene expression data normalization

The raw gene expression data were at first preprocessed by quartile normalization. Then, the RMA (robust multi‐array average) values of every gene (17,318 measured genes) were adjusted for a set of technical covariates (e.g., batch, details in Supplementary Table S5) by fitting linear mixed regression (LME) models. Imputed blood cell counts (i.e., white blood cell [WBC], red blood cell [RBC], platelet, lymphocyte, monocyte, eosinophil, and basophil) (Joehanes R, in preparation) were also evaluated as covariates and adjusted if deemed significant, as detailed below. The residuals were retained for further analysis.

Influence of blood cell types on mRNA expression

Gene expression levels were measured from whole blood, which contains multiple cell types. We used LME models to test the associations between cell types and transcript levels. A large proportion of transcripts were found to be associated with cell‐type proportions. The top three cell types are white blood cells, neutrophils, and lymphocytes. To further evaluate how differences in cell‐type proportions affect the BP‐associated genes at the level of single genes and the coexpression modules identified in this study, we conducted our overall analysis both with and without accounting for cell‐type effects to capture both cell type‐dependent and cell type‐independent BP‐associated genes and processes. We report both results but focus our discussions on those from the adjusted analyses.

Identification of differentially expressed genes for BP traits

The association between gene expression residuals (see in ‘Gene expression data normalization’) and BP traits (SBP, DBP, and HTN) was tested by a linear mixed model adjusting for age, sex, MI, cell types, and familial relatedness in the FHS families. As a secondary analysis, the association between gene expression residuals and BP traits was tested by a linear mixed model adjusting for age, sex, BMI, and familial relatedness, but not adjusting for cell types. Association analysis was conducted using the Kinship package in R (http://cran.r-project.org/web/packages/kinship/) (Abecasis et al, 2001). The BP signature genes were chosen at Bonferroni‐corrected P < 0.05 (corrected for 17,318 measured genes).

Constructing gene coexpression networks and identifying BP‐associated coexpression network modules

Gene coexpression networks were constructed using weighted gene coexpression network analysis (WGCNA) (Zhang & Horvath, 2005; Langfelder & Horvath, 2008). The WGCNA R package uses a fitting index to evaluate a scale‐free network structure built upon Pearson's gene–gene correlations from gene expression variances among individuals (Zhang & Horvath, 2005). Genes were grouped based on the topological overlap of their connectivity using average linkage hierarchical clustering (Zhang & Horvath, 2005), followed by a dynamic cut‐tree algorithm to dynamically cut the clustering dendrogram branches into gene coexpression network modules (coEMs) (Langfelder et al, 2008).

The coexpression network was constructed using the gene expression data from all 3,679 individuals who were not on antihypertensive treatment, rather than on normotensive and hypertensive individuals separately. Inclusion of all individuals across the full spectrum of BP variability increases our power to capture coregulated genes associated with BP variability. In order to minimize the effects from other covariates of BP that may affect the network structure, the gene expression data were pre‐adjusted for BP covariates including age, sex, BMI, cell types, and cohort (offspring vs. third‐generation). The residuals were kept for the coexpression network construction (see ‘Gene expression data normalization’). First, we built weighted gene coexpression networks and identified coEMs that fit a scale‐free topological structure by fitting the index R 2  > 0.8 of the linear model that regressed log(p(k)) on log(k), where k is the connectivity of every node (gene) in the network and p(k) is the frequency distribution of connectivity. The fitting index of a perfect scale‐free network is 1. The relations of coEMs to BP phenotypes were evaluated by correlating the eigengene (first principle component) of each coEM with SBP and DBP across all 3,679 participants via Pearson's correlation testing; P < 0.05 was considered significant.

Identification and collection of whole blood eSNPs

The eSNPs of whole blood used in this study were combined from: (1) eSNPs identified from FHS whole blood gene expression (~18,000 genes) and genotype data (~8 million SNPs after imputation to the 1,000 Genomes reference panel) (Joehanes R, in preparation), and (2) eSNPs identified from other published resources (Emilsson et al, 2008; Fehrmann et al, 2011; Lappalainen et al, 2013; Westra et al, 2013; Battle et al, 2014; Wright et al, 2014).

The FHS blood eQTLs were generated using data from 5,257 FHS participants with genome‐wide genotype data and gene expression profiling. DNA isolation, and genotyping with the Affymetrix 500K mapping array and the Affymetrix 50 K gene‐focused MIP array have been described previously (Levy et al, 2009). Imputation of ~36.3 million SNPs in 1,000 Genomes Phase 1 SNP data was conducted using MACH (Li et al, 2010). For the eQTL identification, we used the 1,000 Genome resource‐imputed SNPs with minor allele frequency (MAF) > 0.01 and imputation ratio > 0.3, yielding approximately 8 million SNPs for eQTL analysis. A pedigree‐based linear mixed model was used to determine the association between each gene expression value and the imputed SNP genotypes by adjusting for age, sex, technical covariates, cell types, and familial relatedness. The cis‐eSNPs (or eQTLs) were constrained by a 1‐megabyte (Mb) window on either side of the transcription start site (TSS). The remaining eSNPs were defined as trans‐eSNPs. Genomic coordinates were based on NCBI human reference genome build 37/hg19. The Benjamini–Hochberg method (BH) (Benjamini & Hochberg, 1995) was used to calculate false discovery rates (FDR) of cis‐ and trans‐eQTLs separately. We only considered eQTLs (both cis and trans) at FDR < 0.1 in each of the blood eQTL studies.

SNP set enrichment analysis (SSEA)

SSEA was used to determine whether a group of eSNPs corresponding to a gene set was enriched for SNPs with low BP association P‐values in GWAS (Zhong et al, 2010; Mäkinen et al, 2014). A gene set that passed SSEA testing was considered as a potential causal gene set. The GWAS used in the current investigation was from the International Consortium of Blood Pressure (ICBP) GWAS for SBP and DBP (Ehret et al, 2011). We first mapped genes within the BP signature gene set or BP coEMs to eSNPs and retrieved the BP association P‐value for every eSNP. Then, we refined the eSNPs of the gene set by only keeping one eSNP for eSNP pairs in linkage disequilibrium (LD, defined as pairwise r 2  ≥ 0.8). The GWAS association P‐values of this group of refined eSNPs were denoted as P geneset. The deviation of P geneset from the null distribution of all eSNPs (limited to eSNPs with LD r 2  < 0.8) toward a lower P‐value was evaluated by both the Kolmogorov–Smirnov (KS) test to derive P KS and Fisher's exact test to obtain P Fisher. In order to perform Fisher's exact test, we categorized all eSNPs into significant and nonsignificant categories based on their association with BP using a BP GWAS P value threshold of P < 0.05.

For each gene set and each statistical test (KS or Fisher's exact test), we computed empirically derived enrichment P‐values based on 1,000 permutations. Each permutation involved random sampling of equal number of genes matching the gene set being tested. Each permutation gene set was subject to the same KS or Fisher's exact test as was used for the testing gene set. The empirically derived P‐value was estimated as the number of permutation gene sets with P‐values less than the observed P‐value of a given gene set/1,000. The BP gene set or a coexpression module was considered to be genetically inferred causal for BP if it demonstrated overall enrichment with GWAS eSNPs showing low P‐value associations with SBP or DBP at Bonferroni‐corrected P KS and P Fisher < 0.05 (corrected for seven gene sets including one BP signature gene set and six BP coEMs).

Molecular network models from orthogonal studies

We compiled both literature‐based and data‐driven molecular networks including gene regulatory networks and protein–protein interaction (PPI) networks. The data‐driven networks were Bayesian networks (BNs) constructed from blood tissue from a human dataset (Emilsson et al, 2008) using a BN modeling method (Zhu et al, 2004, 2007). The BN modeling methods deduce gene regulatory network structure in the transcriptome‐wide gene expression data using a Markov chain Monte Carlo (MCMC) approach and use genetic data as prior information to infer directionality between genes (Zhu et al, 2004, 2007).

The literature‐driven network used in the current study is the PPI network downloaded from the Human Protein Reference Database (HPRD) (Keshava Prasad et al, 2009). PPIs in HPRD were manually curated from literature by biologists. We also downloaded PPI network from BioGrid (Chatr‐Aryamontri et al, 2013), also based on PPIs curated from literature as a comparison with HPRD.

Key driver (KD) analysis

For the genetically inferred causal BP gene sets identified by SSEA, we integrated the genes with molecular networks (BNs and PPI networks as described above) to identify key regulators of every BP gene set using KD analysis. The objective of KD analysis was to identify the important genes for a gene set with respect to a given network structure. A KD of a BP causal gene set is defined as a gene whose neighbor genes in the network are significantly enriched for genes in the BP gene set. As illustrated in Supplementary Fig S7, in order to test whether gene G in a network (a BN or PPI network) is a KD or not, first, we identified the subnetwork of G by retrieving its directly connected genes (1st‐layer neighbor genes), the genes connected by its 1st‐layer neighbor genes (2nd‐layer neighbor genes), and the genes connected by its 2nd‐layer neighbor genes (3rd‐layer neighbor genes). Next, we used Fisher's exact test to evaluate whether the genes in the subnetwork of G (1st‐ to 3rd‐layer neighbor genes of G) show enrichment for genes in the BP causal gene set to derive a KD‐enrichment P‐value. A G that reached a Bonferroni‐corrected KD‐enrichment P < 0.05 was reported as a KD (after correction for the number of genes in the 3rd‐layer expanding network of the tested BP causal gene set).

After the identification of KDs for each BP causal coEMs in each network (BNs and PPI network), KDs were further ranked by leveraging: (1) the BP association P‐values of the eSNPs in the KD based on results from the ICBP BP GWAS (Ehret et al, 2011); (2) the differential expression association P‐value for BP from transcriptome‐wide differential expression analysis in the single‐gene level; and (3) the KD‐enrichment P‐values.

Gene ontology analysis

Each BP gene set identified in this study was classified using Gene Ontology (GO)—biology process categories to define biological process enrichment (Ashburner et al, 2000). One‐sided Fisher's exact test was performed to calculate enrichment P‐values. The P‐value was further corrected by the number of unique GO biological process terms (N = 825). A threshold of P < 6e‐5 was considered significant.

Mouse models for validation of Sh2b3

All animal procedures were approved by Vanderbilt University's Institutional Animal Care and Use Committee, and mice were housed and cared for in accordance with the Guide for the Care and Use of Laboratory Animals. Wild‐type (WT) C57Bl/6J mice were purchased from Jackson Laboratories. Sh2b3‐deficient mice (Sh2b3 −/−) were provided by Dr. Satoshi Takaki (International Medical Center of Japan, Tokyo, Japan) and generated as previously described (Takaki et al, 2000). Exons 3–8 of the gene were knocked out by a genetic recombination technology. These mice were backcrossed with C57Bl/6J for > 10 generations.

RNA sequencing of whole blood samples from mouse models

RNA samples from whole blood were extracted from 4 WT and 4 Sh2b3 −/− mice. Mouse blood total RNA was isolated using a RiboPure™ RNA Purification Kit (Cat# AM1928, Life Technologies, Carlsbad, CA) with an RNase‐free DNase treatment per the manufacturer's instructions. cDNA library construction and RNA sequencing were performed by VANTAGE (Vanderbilt Technologies for Advanced Genomics, Vanderbilt University Medical Center, Nashville, TN). Library preparation was performed using the Illumina TruSeq Stranded mRNA Sample Preparation Kit, and Rev. D of the protocol. Samples were sequenced on the Illumina HiSeq 2500 using v3 SBS chemistry. Libraries were sequenced on a Single Read 50 bp run at 30 million passing filter reads/sample. Details of RNA sequencing protocols were available on: http://vantage.vanderbilt.edu/resources/grant-text/.

RNA sequencing data analysis

Quality control (QC) of the RNA‐Seq reads from FASTQ files was performed by FASTX‐Toolkit package (http://hannonlab.cshl.edu/fastx_toolkit/), and 99.8% reads passed QC by filtering out reads of quality score < 28 and length < 30 bp. The RNA‐Seq reads passing QC were mapped to the mouse reference genome (UCSC mm10) using Tophat v2.0 (Trapnell et al, 2009). Duplicated reads with identical external coordinates were further removed from the output binary sequence alignment (BAM) format files using SAMtools (samtools rmdup command) (Li et al, 2009). Cufflinks v2.2 was used to estimate and normalize mRNA abundances in the form of FPRM (expected number of fragments per kilobase of transcript sequence per millions base pairs sequenced) values (Trapnell et al, 2010). Cuffdiff (Trapnell et al, 2010) was used to identify differentially expressed genes between WT and Sh2b3 −/− groups. Multiple testing was corrected using the q value approach, and the significant threshold of differentially expressed genes was set to be q value < 0.05 (Storey & Tibshirani, 2003).

Data availability

The gene expression data and phenotypes of Framingham Heart Study participants are available online in dbGaP (http://www.ncbi.nlm.nih.gov/gap; accession number phs000007). The RNA sequencing data of wild‐type and Sh2b3 −/− mice are accessible through the GEO accession number GSE65348.

Author contributions

DL and XY designed, directed, and supervised the project. TH, XY, and DL drafted the manuscript. MM, DH, MS, and NE designed and conducted knockout mouse experiments. NR, RW, and PL conducted the gene expression microarray experiments. TH, QM, DJ, BC, and SY conducted the analyses. DL, XY, JZ, BZ, AJ, CO, RV, and PM directed the design of analysis approaches. All authors participated in revising and editing the manuscript. All authors have read and approved the final version of the manuscript.

Conflict of interest

The authors declare that they have no conflict of interest.

Supporting information

Supplementary Figure S1

Click here for additional data file. (86.7KB, pdf)

Supplementary Figure S2

Click here for additional data file. (109.6KB, pdf)

Supplementary Figure S3

Click here for additional data file. (107.6KB, pdf)

Supplementary Figure S4

Click here for additional data file. (61.4KB, pdf)

Supplementary Figure S5

Click here for additional data file. (1.9MB, pdf)

Supplementary Figure S6

Click here for additional data file. (186.8KB, pdf)

Supplementary Figure S7

Click here for additional data file. (40.3KB, pdf)

Supplementary Table S1

Click here for additional data file. (10KB, xlsx)

Supplementary Table S2

Click here for additional data file. (11.1KB, xlsx)

Supplementary Table S3

Click here for additional data file. (12.6KB, xlsx)

Supplementary Table S4

Click here for additional data file. (10.2KB, xlsx)

Supplementary Table S5

Click here for additional data file. (10.2KB, xlsx)

Supplementary Dataset S1

Click here for additional data file. (28.1KB, xlsx)

Supplementary Dataset S2

Click here for additional data file. (24.4KB, xlsx)

Supplementary Dataset S3

Click here for additional data file. (105.7KB, xlsx)

Supplementary Dataset S4

Click here for additional data file. (35.3KB, xlsx)

Supplementary Dataset S5

Click here for additional data file. (254.6KB, xlsx)

Review Process File

Click here for additional data file. (1.4MB, pdf)

Acknowledgements

The Framingham Heart Study is funded by National Institutes of Health contract N01‐HC‐25195. The laboratory work for this investigation was funded by the Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health (Dr. Daniel Levy), and NIH grant K08HL121671 (Dr. Meena Madhur). The analytical component of this project was funded by the Division of Intramural Research, National Heart, Lung, and Blood Institute, the Center for Information Technology, National Institutes of Health, Bethesda, MD (Dr. Daniel Levy), and the American Heart Association Scientist Development Grant 13SDG17290032 (Dr. Xia Yang).

Mol Syst Biol. (2015) 11: 799

References

  1. Abecasis GR, Cardon LR, Cookson WO, Sham PC, Cherny SS (2001) Association analysis in a variance components framework. Genet Epidemiol 21(Suppl 1): S341–S346 [DOI] [PubMed] [Google Scholar]
  2. Ardanaz N, Yang X‐P, Cifuentes ME, Haurani MJ, Jackson KW, Liao T‐D, Carretero OA, Pagano PJ (2010) Lack of glutathione peroxidase 1 accelerates cardiac‐specific hypertrophy and dysfunction in angiotensin II hypertension. Hypertension 55: 116–123 [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT, Harris MA, Hill DP, Issel‐Tarver L, Kasarskis A, Lewis S, Matese JC, Richardson JE, Ringwald M, Rubin GM, Sherlock G (2000) Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 25: 25–29 [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Atkinson C, Stewart S, Upton PD, Machado R, Thomson JR, Trembath RC, Morrell NW (2002) Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor. Circulation 105: 1672–1678 [DOI] [PubMed] [Google Scholar]
  5. Barabási A‐L, Gulbahce N, Loscalzo J (2011) Network medicine: a network‐based approach to human disease. Nat Rev Genet 12: 56–68 [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Barhoumi T, Kasal DA, Li MW, Shbat L, Laurant P, Neves MF, Paradis P, Schiffrin EL (2011) T Regulatory lymphocytes prevent angiotensin ii–induced hypertension and vascular injury. Hypertension 57: 469–476 [DOI] [PubMed] [Google Scholar]
  7. Battle A, Mostafavi S, Zhu X, Potash JB, Weissman MM, McCormick C, Haudenschild CD, Beckman KB, Shi J, Mei R (2014) Characterizing the genetic basis of transcriptome diversity through RNA‐sequencing of 922 individuals. Genome Res 24: 14–24 [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Ser B 57: 289–300 [Google Scholar]
  9. Bernal‐Mizrachi C, Weng S, Feng C, Finck BN, Knutsen RH, Leone TC, Coleman T, Mecham RP, Kelly DP, Semenkovich CF (2003) Dexamethasone induction of hypertension and diabetes is PPAR‐α dependent in LDL receptor–null mice. Nat Med 9: 1069–1075 [DOI] [PubMed] [Google Scholar]
  10. Bernal‐Mizrachi C, Xiaozhong L, Yin L, Knutsen RH, Howard MJ, Arends JJ, DeSantis P, Coleman T, Semenkovich CF (2007) An afferent vagal nerve pathway links hepatic PPARα activation to glucocorticoid‐induced insulin resistance and hypertension. Cell Metab 5: 91–102 [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Chatr‐Aryamontri A, Breitkreutz BJ, Heinicke S, Boucher L, Winter A, Stark C, Nixon J, Ramage L, Kolas N, O'Donnell L, Reguly T, Breitkreutz A, Sellam A, Chen D, Chang C, Rust J, Livstone M, Oughtred R, Dolinski K, Tyers M (2013) The BioGRID interaction database: 2013 update. Nucleic Acids Res 41: D816–D823 [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Chen Y, Zhu J, Lum PY, Yang X, Pinto S, MacNeil DJ, Zhang C, Lamb J, Edwards S, Sieberts SK, Leonardson A, Castellini LW, Wang S, Champy MF, Zhang B, Emilsson V, Doss S, Ghazalpour A, Horvath S, Drake TA et al (2008) Variations in DNA elucidate molecular networks that cause disease. Nature 452: 429–435 [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Cho HM, Lee DY, Kim HY, Lee HA, Seok YM, Kim IK (2012) Upregulation of the Na(+)‐K(+)‐2Cl(‐) cotransporter 1 via histone modification in the aortas of angiotensin II‐induced hypertensive rats. Hypertens Res 35: 819–824 [DOI] [PubMed] [Google Scholar]
  14. Choate KA, Kahle KT, Wilson FH, Nelson‐Williams C, Lifton RP (2003) WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl‐ ‐transporting epithelia. Proc Natl Acad Sci USA 100: 663–668 [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Choi HJ, Yun HS, Kang HJ, Ban H‐J, Kim Y, Nam H‐Y, Hong E‐J, Jung S‐Y, Jung SE, Jeon J‐P (2012) Human transcriptome analysis of acute responses to glucose ingestion reveals the role of leukocytes in hyperglycemia‐induced inflammation. Physiol Genomics 44: 1179–1187 [DOI] [PubMed] [Google Scholar]
  16. Civelek M, Lusis AJ (2014) Systems genetics approaches to understand complex traits. Nat Rev Genet 15: 34–48 [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Connolly MJ, Aaronson PI (2011) Key role of the RhoA/Rho kinase system in pulmonary hypertension. Pulm Pharmacol Ther 24: 1–14 [DOI] [PubMed] [Google Scholar]
  18. Cunningham JT, Fleming T, Penny ML, Herrera‐Rosales M, Mifflin SW (2006) Increased c‐Fos in medullary cardiovascular nuclei in acute and chronic renal wrap hypertension. FASEB J 20: A1205–A1206 [Google Scholar]
  19. Cusick ME, Klitgord N, Vidal M, Hill DE (2005) Interactome: gateway into systems biology. Hum Mol Genet 14: R171–R181 [DOI] [PubMed] [Google Scholar]
  20. Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg‐Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y et al (2011) Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 478: 103–109 [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Ehret GB, Caulfield MJ (2013) Genes for blood pressure: an opportunity to understand hypertension. Eur Heart J 34: 951–961 [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Emilsson V, Thorleifsson G, Zhang B, Leonardson AS, Zink F, Zhu J, Carlson S, Helgason A, Walters GB, Gunnarsdottir S, Mouy M, Steinthorsdottir V, Eiriksdottir GH, Bjornsdottir G, Reynisdottir I, Gudbjartsson D, Helgadottir A, Jonasdottir A, Styrkarsdottir U, Gretarsdottir S et al (2008) Genetics of gene expression and its effect on disease. Nature 452: 423–428 [DOI] [PubMed] [Google Scholar]
  23. Fehrmann RS, Jansen RC, Veldink JH, Westra H‐J, Arends D, Bonder MJ, Fu J, Deelen P, Groen HJ, Smolonska A (2011) Trans‐eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. PLoS Genet 7: e1002197 [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Feinleib M, Kannel WB, Garrison RJ, McNamara PM, Castelli WP (1975) The Framingham offspring study. Design and preliminary data. Prev Med 4: 518–525 [DOI] [PubMed] [Google Scholar]
  25. Goh K‐I, Cusick ME, Valle D, Childs B, Vidal M, Barabási A‐L (2007) The human disease network. Proc Natl Acad Sci 104: 8685–8690 [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Groop LC, Kankuri M, Schalin‐Jantti C, Ekstrand A, Nikula‐Ijas P, Widen E, Kuismanen E, Eriksson J, Franssila‐Kallunki A, Saloranta C (1993) Association between polymorphism of the glycogen synthase gene and non‐insulin‐dependent diabetes mellitus. N Engl J Med 328: 10–14 [DOI] [PubMed] [Google Scholar]
  27. Guzik TJ, Hoch NE, Brown KA, McCann LA, Rahman A, Dikalov S, Goronzy J, Weyand C, Harrison DG (2007) Role of the T cell in the genesis of angiotensin II induced hypertension and vascular dysfunction. J Exp Med 204: 2449–2460 [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Hamid R, Cogan JD, Hedges LK, Austin E, Phillips JA, Newman JH, Loyd JE (2009) Penetrance of Pulmonary Arterial Hypertension Is Modulated by the Expression of Normal BMPR2 Allele. Hum Mutat 30: 649–654 [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Harrison DG, Vinh A, Lob H, Madhur MS (2010) Role of the adaptive immune system in hypertension. Curr Opin Pharmacol 10: 203–207 [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Harrison DG, Guzik TJ, Lob HE, Madhur MS, Marvar PJ, Thabet SR, Vinh A, Weyand CM (2011) Inflammation, immunity, and hypertension. Hypertension 57: 132–140 [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Harrison DG, Marvar PJ, Titze JM (2012) Vascular inflammatory cells in hypertension. Front Physiol 3: 128 [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Hiebert PR, Granville DJ (2012) Granzyme B in injury, inflammation, and repair. Trends Mol Med 18: 732–741 [DOI] [PubMed] [Google Scholar]
  33. Huan T, Zhang B, Wang Z, Joehanes R, Zhu J, Johnson AD, Ying S, Munson PJ, Raghavachari N, Wang R, Liu P, Courchesne P, Hwang SJ, Assimes TL, McPherson R, Samani NJ, Schunkert H, Meng Q, Suver C, O'Donnell CJ et al (2013) A systems biology framework identifies molecular underpinnings of coronary heart disease. Arterioscler Thromb Vasc Biol 33: 1427–1434 [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Joehanes R, Ying S, Huan T, Johnson AD, Raghavachari N, Wang R, Liu P, Woodhouse KA, Sen SK, Tanriverdi K (2013a) Gene expression signatures of coronary heart disease. Arterioscler Thromb Vasc Biol 33: 1418–1426 [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Joehanes R, Huan T, Yao C, Zhang X, Ying S, Feolo M, Sharapova N, Przytycka T, Sturcke A, Schaffer AA, Heard‐Costa N, Liu P, Wang R, Woodhouse KA, Raghavachari N, Dupuis J, Johnson AD, O'Donnell CJ, Munson PJ, Levy D (2013b) Genome‐wide Expression Quantitative Trait Loci: Results from the NHLBI's SABRe CVD Initiative. The American Society of Human Genetics (ASHG) conference; Oct 22–26 2013; Boston Convention Ctr. Boston, MA
  36. Kearney PM, Whelton M, Reynolds K, Muntner P, Whelton PK, He J (2005) Global burden of hypertension: analysis of worldwide data. Lancet 365: 217–223 [DOI] [PubMed] [Google Scholar]
  37. Keshava Prasad TS, Goel R, Kandasamy K, Keerthikumar S, Kumar S, Mathivanan S, Telikicherla D, Raju R, Shafreen B, Venugopal A, Balakrishnan L, Marimuthu A, Banerjee S, Somanathan DS, Sebastian A, Rani S, Ray S, Harrys Kishore CJ, Kanth S, Ahmed M et al (2009) Human Protein Reference Database–2009 update. Nucleic Acids Res 37: D767–D772 [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Kirabo A, Fontana V, de Faria AP, Loperena R, Galindo CL, Wu J, Bikineyeva AT, Dikalov S, Xiao L, Chen W (2014) DC isoketal‐modified proteins activate T cells and promote hypertension. J Clin Investig 124 [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Kokubo Y, Tomoike H, Tanaka C, Banno M, Okuda T, Inamoto N, Kamide K, Kawano Y, Miyata T (2006) Association of sixty‐one non‐synonymous polymorphisms in forty‐one hypertension candidate genes with blood pressure variation and hypertension. Hypertens Res 29: 611–619 [DOI] [PubMed] [Google Scholar]
  40. Koschinsky ML, Boffa MB, Nesheim ME, Zinman B, Hanley AJ, Harris SB, Cao H, Hegele RA (2001) Association of a single nucleotide polymorphism in CPB2 encoding the thrombin‐activable fibrinolysis inhibitor (TAF1) with blood pressure. Clin Genet 60: 345–349 [DOI] [PubMed] [Google Scholar]
  41. Langfelder P, Horvath S (2008) WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics 9: 559 [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Langfelder P, Zhang B, Horvath S (2008) Defining clusters from a hierarchical cluster tree: the Dynamic Tree Cut package for R. Bioinformatics 24: 719–720 [DOI] [PubMed] [Google Scholar]
  43. Lappalainen T, Sammeth M, Friedländer MR, AC't HP, Monlong J, Rivas MA, Gonzàlez‐Porta M, Kurbatova N, Griebel T, Ferreira PG (2013) Transcriptome and genome sequencing uncovers functional variation in humans. Nature 501: 506–511 [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Lawes CM, Vander Hoorn S, Law MR, Elliott P, MacMahon S, Rodgers A (2006) Blood pressure and the global burden of disease 2000. Part II: estimates of attributable burden. J Hypertens 24: 423–430 [DOI] [PubMed] [Google Scholar]
  45. Lee H‐A, Cho H‐M, Lee D‐Y, Kim K‐C, Han HS, Kim IK (2012) Tissue‐specific upregulation of angiotensin‐converting enzyme 1 in spontaneously hypertensive rats through histone code modifications. Hypertension 59: 621–626 [DOI] [PubMed] [Google Scholar]
  46. Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Kottgen A, Vasan RS, Rivadeneira F, Eiriksdottir G, Guo X, Arking DE, Mitchell GF, Mattace‐Raso FU et al (2009) Genome‐wide association study of blood pressure and hypertension. Nat Genet 41: 677–687 [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Lewington S, Clarke R, Qizilbash N, Peto R, Collins R (2002) Age‐specific relevance of usual blood pressure to vascular mortality: a meta‐analysis of individual data for one million adults in 61 prospective studies. Lancet 360: 1903–1913 [DOI] [PubMed] [Google Scholar]
  48. Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R (2009) The sequence alignment/map format and SAMtools. Bioinformatics 25: 2078–2079 [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR (2010) MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 34: 816–834 [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Lindgren CM, Nilsson A, Orho‐Melander M, Almgren P, Groop LC (2001) Characterization of the annexin I gene and evaluation of its role in type 2 diabetes. Diabetes 50: 2402–2405 [DOI] [PubMed] [Google Scholar]
  51. Lou Y, Liu J, Huang Y, Liu J, Wang Z, Liu Y, Li Z, Li Y, Xie Y, Wen S (2010) A46G and C79G polymorphisms in the β2‐adrenergic receptor gene (ADRB2) and essential hypertension risk: a meta‐analysis. Hypertens Res 33: 1114–1123 [DOI] [PubMed] [Google Scholar]
  52. Mäkinen V‐P, Civelek M, Meng Q, Zhang B, Zhu J, Levian C, Huan T, Segrè AV, Ghosh S, Vivar J (2014) Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease. PLoS Genet 10: e1004502 [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Marks AR (2003) Calcium and the heart: a question of life and death. J Clin Investig 111: 597 [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Marvar PJ, Thabet SR, Guzik TJ, Lob HE, McCann LA, Weyand C, Gordon FJ, Harrison DG (2010) Central and peripheral mechanisms of T‐lymphocyte activation and vascular inflammation produced by angiotensin II‐induced hypertension. Circ Res 107: 263–270 [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Maunakea AK, Chepelev I, Zhao K (2010) Epigenome mapping in normal and disease States. Circ Res 107: 327–339 [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Minson J, Arnolda L, Llewellyn‐Smith I, Pilowsky P, Chalmers J (1996) Altered c‐fos in rostral medulla and spinal cord of spontaneously hypertensive rats. Hypertension 27: 433–441 [DOI] [PubMed] [Google Scholar]
  57. Oishi Y, Manabe I, Imai Y, Hara K, Horikoshi M, Fujiu K, Tanaka T, Aizawa T, Kadowaki T, Nagai R (2010) Regulatory polymorphism in transcription factor KLF5 at the MEF2 element alters the response to angiotensin II and is associated with human hypertension. FASEB J 24: 1780–1788 [DOI] [PubMed] [Google Scholar]
  58. Orho‐Melander M, Almgren P, Kanninen T, Forsblom C, Groop LC (1999) A paired‐sibling analysis of the XbaI polymorphism in the muscle glycogen synthase gene. Diabetologia 42: 1138–1145 [DOI] [PubMed] [Google Scholar]
  59. Saleh MA, McMaster WG, Wu J, Norlander AE, Funt SA, Thabet SR, Kirabo A, Xiao L, Chen W, Itani HA, Michell D, Huan T, Zhang Y, Titze J, Levy D, Harrison DG, Madhur MS (2015) Lymphocyte adaptor protein LNK deficiency exacerbates hypertension and end‐organ inflammation. J Clin Investig 125: 1189–1202 [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Satou R, Miyata K, Gonzalez‐Villalobos RA, Ingelfinger JR, Navar LG, Kobori H (2012) Interferon‐γ biphasically regulates angiotensinogen expression via a JAK‐STAT pathway and suppressor of cytokine signaling 1 (SOCS1) in renal proximal tubular cells. FASEB J 26: 1821–1830 [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Shanmugam N, Todorov I, Nair I, Omori K, Reddy M, Natarajan R (2006) Increased expression of cyclooxygenase‐2 in human pancreatic islets treated with high glucose or ligands of the advanced glycation endproduct‐specific receptor (AGER), and in islets from diabetic mice. Diabetologia 49: 100–107 [DOI] [PubMed] [Google Scholar]
  62. Splansky GL, Corey D, Yang Q, Atwood LD, Cupples LA, Benjamin EJ, D'Agostino RB Sr, Fox CS, Larson MG, Murabito JM, O'Donnell CJ, Vasan RS, Wolf PA, Levy D (2007) The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: design, recruitment, and initial examination. Am J Epidemiol 165: 1328–1335 [DOI] [PubMed] [Google Scholar]
  63. Storey JD, Tibshirani R (2003) Statistical significance for genomewide studies. Proc Natl Acad Sci 100: 9440–9445 [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Tabara Y, Kohara K, Kita Y, Hirawa N, Katsuya T, Ohkubo T, Hiura Y, Tajima A, Morisaki T, Miyata T (2010) Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension The Japanese Millennium Genome Project. Hypertension 56: 973–980 [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Takaki S, Sauer K, Iritani BM, Chien S, Ebihara Y, Tsuji K, Takatsu K, Perlmutter RM (2000) Control of B cell production by the adaptor protein lnk. Definition Of a conserved family of signal‐modulating proteins. Immunity 13: 599–609 [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Takizawa H, Eto K, Yoshikawa A, Nakauchi H, Takatsu K, Takaki S (2008) Growth and maturation of megakaryocytes is regulated by Lnk/Sh2b3 adaptor protein through crosstalk between cytokine‐and integrin‐mediated signals. Exp Hematol 36: 897–906 [DOI] [PubMed] [Google Scholar]
  67. Tang C, Oram JF (2009) The cell cholesterol exporter ABCA1 as a protector from cardiovascular disease and diabetes. Biochim Biophys Acta 1791: 563–572 [DOI] [PubMed] [Google Scholar]
  68. Trapnell C, Pachter L, Salzberg SL (2009) TopHat: discovering splice junctions with RNA‐Seq. Bioinformatics 25: 1105–1111 [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Trapnell C, Williams BA, Pertea G, Mortazavi A, Kwan G, van Baren MJ, Salzberg SL, Wold BJ, Pachter L (2010) Transcript assembly and quantification by RNA‐Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat Biotechnol 28: 511–515 [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Wang IM, Zhang B, Yang X, Zhu J, Stepaniants S, Zhang C, Meng Q, Peters M, He Y, Ni C, Slipetz D, Crackower MA, Houshyar H, Tan CM, Asante‐Appiah E, O'Neill G, Luo MJ, Thieringer R, Yuan J, Chiu CS et al (2012) Systems analysis of eleven rodent disease models reveals an inflammatome signature and key drivers. Mol Syst Biol 8: 594 [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Westra H‐J, Peters MJ, Esko T, Yaghootkar H, Schurmann C, Kettunen J, Christiansen MW, Fairfax BP, Schramm K, Powell JE (2013) Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat Genet 45: 1238–1243 [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Wright FA, Sullivan PF, Brooks AI, Zou F, Sun W, Xia K, Madar V, Jansen R, Chung W, Zhou Y‐H (2014) Heritability and genomics of gene expression in peripheral blood. Nat Genet 46: 430–437 [DOI] [PMC free article] [PubMed] [Google Scholar]
  73. Zhang B, Gaiteri C, Bodea LG, Wang Z, McElwee J, Podtelezhnikov AA, Zhang C, Xie T, Tran L, Dobrin R, Fluder E, Clurman B, Melquist S, Narayanan M, Suver C, Shah H, Mahajan M, Gillis T, Mysore J, MacDonald ME et al (2013) Integrated systems approach identifies genetic nodes and networks in late‐onset Alzheimer's disease. Cell 153: 707–720 [DOI] [PMC free article] [PubMed] [Google Scholar]
  74. Zhang B, Horvath S (2005) A general framework for weighted gene co‐expression network analysis. Stat Appl Genet Mol Biol 4: Article 17 [DOI] [PubMed] [Google Scholar]
  75. Zhang N (2011) The role of endogenous aryl hydrocarbon receptor signaling in cardiovascular physiology. J Cardiovasc Dis Res 2: 91–95 [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Zhong H, Yang X, Kaplan LM, Molony C, Schadt EE (2010) Integrating pathway analysis and genetics of gene expression for genome‐wide association studies. Am J Hum Genet 86: 581–591 [DOI] [PMC free article] [PubMed] [Google Scholar]
  77. Zhu J, Lum PY, Lamb J, GuhaThakurta D, Edwards SW, Thieringer R, Berger JP, Wu MS, Thompson J, Sachs AB, Schadt EE (2004) An integrative genomics approach to the reconstruction of gene networks in segregating populations. Cytogenet Genome Res 105: 363–374 [DOI] [PubMed] [Google Scholar]
  78. Zhu J, Wiener MC, Zhang C, Fridman A, Minch E, Lum PY, Sachs JR, Schadt EE (2007) Increasing the power to detect causal associations by combining genotypic and expression data in segregating populations. PLoS Comput Biol 3: e69 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Figure S1

Click here for additional data file. (86.7KB, pdf)

Supplementary Figure S2

Click here for additional data file. (109.6KB, pdf)

Supplementary Figure S3

Click here for additional data file. (107.6KB, pdf)

Supplementary Figure S4

Click here for additional data file. (61.4KB, pdf)

Supplementary Figure S5

Click here for additional data file. (1.9MB, pdf)

Supplementary Figure S6

Click here for additional data file. (186.8KB, pdf)

Supplementary Figure S7

Click here for additional data file. (40.3KB, pdf)

Supplementary Table S1

Click here for additional data file. (10KB, xlsx)

Supplementary Table S2

Click here for additional data file. (11.1KB, xlsx)

Supplementary Table S3

Click here for additional data file. (12.6KB, xlsx)

Supplementary Table S4

Click here for additional data file. (10.2KB, xlsx)

Supplementary Table S5

Click here for additional data file. (10.2KB, xlsx)

Supplementary Dataset S1

Click here for additional data file. (28.1KB, xlsx)

Supplementary Dataset S2

Click here for additional data file. (24.4KB, xlsx)

Supplementary Dataset S3

Click here for additional data file. (105.7KB, xlsx)

Supplementary Dataset S4

Click here for additional data file. (35.3KB, xlsx)

Supplementary Dataset S5

Click here for additional data file. (254.6KB, xlsx)

Review Process File

Click here for additional data file. (1.4MB, pdf)

Data Availability Statement

The gene expression data and phenotypes of Framingham Heart Study participants are available online in dbGaP (http://www.ncbi.nlm.nih.gov/gap; accession number phs000007). The RNA sequencing data of wild‐type and Sh2b3 −/− mice are accessible through the GEO accession number GSE65348.

Articles from Molecular Systems Biology are provided here courtesy of Nature Publishing Group

RESOURCES