Data on genetic linkage of oxidative stress with cardiometabolic traits in an intercross derived from hyperlipidemic mouse strains

Abstract

The data presented here are related to the research article, entitled Genetic linkage of oxidative stress with cardiometabolic traits in an intercross derived from hyperlipidemic mouse strains, published in Atherosclerosis 2019 Dec 3;293:1–10 (D. Fuller, A.T. Grainger, A. Manichaikul, W. Shi). The supporting materials include original genotypic and phenotypic data obtained from 266 female F2 mice derived from an intercross between C57BL/6 (B6) and BALB/cJ (BALB) Apoe^−/- mice. F2 mice were fed 12 weeks of Western diet, starting at 6 weeks of age. Plasma levels of HDL, LDL cholesterol, triglycerides, glucose and malondialdehyde (MDA) and atherosclerosis in the aortic root and the left carotid artery were measured. 127 microsatellite markers across the entire genome were genotyped. The data is provided in the format ready for QTL analysis with J/qtl and MapManager QTX.

Specifications Table

Subject	Biochemistry, Genetics and Molecular Biology
Specific subject area	QTL analysis of oxidative stress
Type of data	Tables
How data were acquired	Plasma levels of malondialdehyde (MDA), total and HDL cholesterol, triglyceride, and glucose levels were measured with assay kits. Atherosclerotic lesion sizes in the aortic root and the left carotid artery were quantified with AxioVision version 4.8 software on oil red O stained sections. 127 microsatellite markers across the entire genome were typed by PCR. J/qtl and Map Manager QTX software was used to find genetic loci for the traits.
Data format	Raw Analysed
Parameters for data collection	Female F2 mice were started with a western diet at 6 weeks of age and remained on the diet for 12 weeks.
Description of data collection	266 female F2 mice were generated from an intercross between C57BL/6 (B6) and BALB/c (BALB) Apoe−/− mice. Fasting blood was collected once before and once after 12 weeks of Western diet. The heart and adjacent aorta and the left carotid artery were harvested and processed for quantification of atherosclerosis.
Data source location	University of Virginia, Charlottesville, Virginia, USA
Data accessibility	With the article.
Related research article	Fuller DT, Grainger AT, Manichaikul A, Shi W. Genetic linkage of oxidative stress with cardiometabolic traits in an intercross derived from hyperlipidemic mouse strains. Atherosclerosis. 2019 Dec 3;293:1–10. https://doi.org/10.1016/j.atherosclerosis.2019.11.034.

Value of the Data •The raw data provided allows other researchers to make comparisons with their own data. •The data allows other researchers to conduct combined cross analyses of genetic loci for cadiometabolic traits in mice. •Plasma levels of total, HDL, non-HDL cholesterol, free cholesterol, and glucose in F2 mice fed a chow diet are also included. These data can be used by others to conduct combined cross analysis of QTLs for these traits and power calculation to estimate the number of animals needed for similar experiments.

1. Data description

The Supplementary data provided here includes both raw data and analysed data used in the Atherosclerosis article [1]. The raw data was obtained from 266 female F2 mice derived from an intercross between C57BL/6 (B6) and BALB/cJ (BALB) Apoe^−/− mice as reported [2] and was formatted for analyses using J/qtl and Map Manager QTX.

2. Experimental design, materials, and methods

2.1. Mice

266 female F2 mice were generated from an intercross between B6-Apoe^−/− and BALB-Apoe^−/− mice as reported [2]. Mice were weaned onto a chow diet at 3 weeks of age and started on a Western diet at 6 weeks of age. After 12 weeks of Western diet, mice were euthanized. Fasting blood was collected under isoflurane anaesthesia, once before and once after 12 weeks of Western diet.

2.2. Phenotypic analyses

Plasma MDA was measured with a Cayman Thiobarbituric Acid Reactive Substances (TBARS) kit (Cat. # 10009055). Plasma glucose was measured with a Sigma assay kit (Cat. # GAHK20). Cholesterol and triglyceride concentrations were measured enzymatically using Thermo DMA (Louisville, CO) kits. Non-HDL cholesterol concentrations were calculated as the difference between total and HDL cholesterol levels. Atherosclerotic lesion sizes in the aortic root and the left carotid artery of F2 mice were measured on oil red O stained sections as we reported [[3], [4], [5], [6], [7]].

2.3. Genotypic analysis

DNA was prepared from tail clips of mice and genotyped as described [[8], [9], [10]]. 127 microsatellite markers across the entire genome at an average interval of 12 cM were typed.

2.4. Statistical analysis

QTL analysis was performed using J/qtl and Map Manager QTX as reported [[11], [12], [13], [14], [15]]. One thousand permutations were run to define the genome-wide LOD (logarithm of odds) score thresholds for significant or suggestive linkage of each trait. Loci exceeding the LOD score threshold of 0.05 were significant (p < 0.05) and those exceeding the threshold of 0.63 were suggestive (p < 0.63). Regression analysis was performed to dissect the contribution of a metabolic trait to the variation in plasma MDA levels of F2 mice.

Conflict of Interests

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Appendix A. Supplementary data

The following is the Supplementary data to this article: