The tumour-suppressive miR-29a/b1 cluster is regulated by CEBPA and blocked in human AML

Abstract

Background:

CCAAT/enhancer-binding protein-α (CEBPA) is crucial for normal granulopoiesis and is frequently disrupted in acute myeloid leukaemia (AML). Increasing evidence suggests that CEBPA exerts its effects, in parts, by regulating specific microRNAs (miRNAs), as previously shown for miR-223. The aim of this study was to investigate the genome-wide pattern of miRNAs regulated by CEBPA in myeloid cells.

Methods:

In Kasumi-1 cells, conditionally expressing CEBPA, we assessed the expression of 470 human miRNAs by microarray analysis. We further investigated the microarray results by qRT-PCR, luciferase reporter assays, and chromatin immunoprecipitation assays.

Results:

In all, 18 miRNAs were more than two-fold suppressed or induced after CEBPA restoration. Among these 18 miRNAs, we focused on CEBPA-mediated regulation of the tumour-suppressive miR-29b. We observed that miR-29b is suppressed in AML patients with impaired CEBPA function or loss of chromosome 7q. We found that CEBPA selectively regulates miR-29b expression on its miR-29a/b1 locus on chromosome 7q32.3, whereas miR-29b2/c on chromosome 1q32.2 is not affected.

Conclusion:

This study reports the activation of the tumour-suppressive miR-29b by the haematopoietic key transcription factor CEBPA. Our data provide a rationale for miR-29b suppression in AML patients with loss of chromosome 7q or CEBPA deficiency.

Haematopoiesis is a highly orchestrated interaction of lineage-specific transcription factors driving pluripotent precursor cells to differentiate towards mature blood cells (Rosenbauer and Tenen, 2007). Increasing evidence suggests that this differentiation along the various haematopoietic lineages is, in part, also regulated by microRNAs (miRNAs) (Lawrie, 2007; Garzon and Croce, 2008; Pelosi et al, 2009). miRNAs are small, non-coding RNAs, which silence target genes by base-pairing to untranslated mRNA regions. Thereby, miRNAs adjust expression of specific transcription factors in a post-transcriptional manner (Shivdasani, 2006; Ambros and Chen, 2007). Deregulation of either haematopoietic transcription factors or miRNAs is a common event in the molecular pathogenesis of human leukaemias (Tenen, 2003; Kluiver et al, 2006; Rosenbauer and Tenen, 2007; Fabbri et al, 2008).

One of the key transcription factors for normal haematopoiesis is the CCAAT/enhancer-binding protein-α (CEBPA). It has been shown to be crucial for myeloid differentiation towards mature granulocytes (Zhang et al, 1997; Radomska et al, 1998). In human acute myeloid leukaemia (AML), CEBPA function is frequently disrupted (Pabst and Mueller, 2007). Approximately 10% of AML patients show dominant-negative mutations in the CEBPA coding region (Pabst et al, 2001b). In addition, CEBPA expression is suppressed by the leukaemogenic fusion proteins AML1-ETO, AML1-MDS1-EVI1, or CBFB-SMMHC in AML patients bearing the chromosomal rearrangements t(8;21), t(3;21) or inv(16) respectively (Pabst et al, 2001a; Helbling et al, 2004, 2005).

During normal haematopoiesis, various CEBPA downstream effectors have been described (Tenen, 2003; Mueller and Pabst, 2006), including so far at least one miRNA (miR-223) (Fazi et al, 2005; Fukao et al, 2007; Eyholzer et al, 2009). The activation of miR-223 by CEBPA can trigger neutrophil differentiation and is necessary for maintaining proper function of mature neutrophils (Fazi et al, 2005, 2007; Johnnidis et al, 2008). On the basis of these reports and the prominent role of CEBPA for normal myelopoiesis, we assessed in this study the genome-wide regulation of miRNAs by CEBPA in myeloid leukaemic cells. We screened 470 human miRNAs for their expression levels in CEBPA-deficient leukaemic Kasumi-1 cells using a conditional CEBPA expression system. We identified 18 miRNAs whose expression levels changed more than two-fold after CEBPA induction. Among them, we identified the tumour-suppressive miR-29a/b1 cluster to be a direct target of CEBPA.

Patients and methods

Patients, controls and cell lines

Bone marrow samples from 66 consecutive AML patients collected at diagnosis before treatment were used, comprising all FAB subtypes. Leukaemic cells were collected using Ficoll gradient (Lymphoprep; Axis-Shield PoC AS, Oslo, Norway). miRNA was extracted using the miRNeasy Mini kit no. 217004 (Qiagen AG, Hombrechtikon, Switzerland). Mature monocytes or granulocytes from six healthy volunteers were isolated from peripheral blood using the EasySep selection kits nos. 18088-CD14 and 18682-CD66b (RoboSep; StemCell Technologies, Vancouver, Canada). CD34+ myeloid stem cells from three patients were enriched using the CliniMacs CD34 Complete kit no. 177–01 (Miltenyi Biotec, Auburn, CA, USA). Informed consent from patients and volunteers was obtained according to the Declaration of Helsinki Principles. Clinical characteristics are summarised in Supplementary Table S1 (Supplementary Material).

Leukaemic Kasumi-1 cells stably transfected with an inducible CEBPA-oestrogen receptor (ER) fusion construct (CEBPA-ER) (Pabst et al, 2001a) were cultured in phenol red-free RPMI 1640 supplemented with 10% foetal calf serum (FCS). The CEBPA-ER fusion protein was activated using 1 μM β-oestradiol. All reagents were from Sigma-Aldrich (Buchs, Switzerland).

Leukaemic U937 cells stably transfected with the tetracycline-inducible (tet-off) oncogenic t(8;21) fusion protein AML1-ETO (Pabst et al, 2001a) were cultured in RPMI 1640 supplemented with 10% FCS and 0.75 μg ml⁻¹ tetracycline. To induce AML1-ETO expression the cells were extensively washed with PBS and cultured in RPMI 1640, supplemented with 10% tetracycline-free FCS (PAA Laboratories GmbH, Pasching, Austria).

Leukaemic HL60, K562, Kasumi-1 and U937 cells, and H1299 lung cancer cells (ATCC, Manassas VA, USA) were cultured in RPMI 1640 with 10% FCS. The cell lines were characterised by molecular diagnostics and cytogenetics, and cell morphology was monitored by microscopy according to ATCC guidelines (http://www.atcc.org >cultures and products > technical support > technical literature > technical bulletin no. 8). No abnormalities in cell morphology were observed in these cell lines, both at low and high densities of cultures during the course of these experiments. Repetitive mycoplasma screening remained negative in these cell lines (PCR mycoplasma test kit Promokine no. PK-CA91–1048; PromoCell GmbH, Heidelberg, Germany).

miRNA microarray

Parental Kasumi-1 and Kasumi-1 cells with the inducible CEBPA-ER construct were collected before and 72 h after β-oestradiol treatment. miRNA was extracted using the miRNeasy mini kit no. 217004 (Qiagen AG), and miRNA quality was determined using Agilent 2100 Bioanalyzer (Agilent Technologies, Basel, Switzerland).

To assess miRNA expression profiles, we used the human miRNA microarray kit no. G4470A, detecting 470 human and 64 viral miRNAs based on the Sanger database version 9.1 (http://www.mirbase.org). Scanning and image analysis were carried out using the Agilent DNA microarray scanner (no. G2565BA; XDR 5/100, single pass, green). Feature Extraction software (version 9.5; Agilent Technologies) was used for data extraction from raw microarray image files using the miRNA_v1_95_May07 FE protocol (grid 016436_D_20070426). Data analysis was carried out using GeneSpring GX 9.0 (Agilent Technologies) expression analysis software and expression values were corrected for oestrogen effects. The cut-off for miRNA candidates was set at more than two-fold changes in expression (suppression or induction) after CEBPA restoration, and such changes had to be observed in two independant experiments. The microarray kit, equipment and software used for these arrays were from Agilent Technologies.

Luciferase reporter assay

The human DNA sequence comprising −682 to +296 bp upstream of the primary miR-29a/b1 transcription start site (GenBank accession number EU154353) was cloned into the pGL3b luciferase vector using KpnI and NheI restriction sites. This construct was co-transfected with a human CEBPA expression plasmid (pcDNA3) in H1299 cells using Lipofectamine 2000 (Invitrogen, Basel, Switzerland). Luminescence was detected using the Dual-Luciferase Reporter Assay (Promega, Dübendorf, Switzerland). Primer sequences are indicated in Supplementary Table S2 (Supplementary Material).

Quantitative RT-PCR

miR-29b expression in samples from AML patients and healthy volunteers was assessed using the miScript SYBR Green PCR kit no. 218073 and primer assay hs-miR-29b no. MS_6566 (Qiagen AG). Expression values were normalised to the geometric mean (Peltier and Latham, 2008) of miR-93 and miR-191 expression (nos. MS_3346 and MS_3682 respectively; Qiagen AG). To distinguish between miR-29a and miR-29c expression, we used TaqMan microRNA assays no. 001212 (29a) and no. 000578 (29c) and TaqMan universal PCR master mix No AmpErase UNG no. 4324018 (Applied Biosystems, Rotkreuz, Switzerland). Primer sequences for pri-miR-29a/b/c detection using QuantiTect SYBR Green PCR kit no. 204143 (Qiagen AG) are indicated in Supplementary Table S2 (Supplementary Material). Expression values of miR-29a/b/c and their primary transcripts in cell line experiments were normalised to miR-93 expression, as miR-93 showed robust and stable expression during the time courses in this study. All qRT-PCR reactions were carried out on 7900HT Fast Real-Time PCR system (Applied Biosystems).

Chromatin immunoprecipitation assay

Chromatin immunoprecipitation assays were performed using the ChIP-IT Express Enzymatic kit no. 53009 (Active Motif, Rixensart, Belgium). Immunoprecipitation of sheared chromatin of parental U937 as well as of Kasumi-1-CEBPA-ER cells collected 72 h after β-oestradiol treatment was performed using antibodies against CEBPA (polyclonal rabbit IgG, sc-61X), polymerase II (sc-900X), and rabbit IgG (sc-2027; all from Santa Cruz, Heidelberg, Germany). Sequences of the PCR primers to detect CEBPA binding to the pri-miR-29a/b1 promoter or to the pre-miR-223 regulatory element as positive control (Fazi et al, 2005) are described in Supplementary Table S2 (Supplementary Material).

Western blot analysis

Protein detection was carried out from whole-cell lysates using antibodies against CEBPA no. 39306 (1:500; Active Motif) and DNMT3B sc-10236 (1:500; Santa Cruz). For loading control, β-actin antibody MAB1501 (1:10⁵; Chemicon/Milipore, Zug, Switzerland) was used. Horseradish-peroxidase-linked secondary antibodies (1:5000 each) were: anti-mouse no. NA931V, anti-rabbit no. NA934V (Amersham, GE Healthcare Bio-sciences, Uppsala, Sweden), and anti-goat sc-2020 (Santa Cruz).

URL and statistical analysis

Conservation studies of the pri-miR-29a/b1 (GenBank accession number EU154353) and pri-miR29b2/c (EU154351 and EU154352) loci were carried out using http://www.genome.ucsc.edu/ (assembly March 2006). Promoter analysis for putative CEBP binding sites were performed using Genomatix MatInspector software, release 7.7(3) (Genomatix Software GmbH, Munich, Germany). Differences in promoter activities and miR-29 expression levels were analysed by t-test, with P<0.05 defining significance using GraphPad Prism software version 4.0 (GraphPad Software Inc., La Jolla, CA, USA).

Results

Genome-wide changes in miRNA expression after CEBPA restoration in human AML

To identify miRNAs regulated by the myeloid key transcription factor CEBPA in the haematopoietic system, we carried out miRNA microarrays assessing 470 human miRNAs. We used leukaemic Kasumi-1 cells lacking detectable amounts of endogenous CEBPA, however, containing an inducible CEBPA-ER fusion construct (Pabst et al, 2001a). We treated these cells with β-oestradiol for 72 h to restore the CEBPA function, and analysed the changes in miRNA expression. We found that the expression of 18 miRNAs changed more than two-fold after restoring CEBPA function compared with untreated Kasumi-1-CEBPA-ER cells and after exclusion of effects because of oestrogen treatment (Table 1). Of the 18 miRNAs, 8 (44%) were suppressed (Table 1A: miR-98, miR-181b, miR-197, miR-210, miR-342, miR-432, miR-550, and miR-776), whereas 10 miRNAs (56%) were induced (Table 1B: miR-29b, miR-223, miR-370, miR-496, miR-572, miR-575 miR-630, miR-638, miR-663, and miR-765; Supplementary Table S3). miR-223, a previously identified target of CEBPA (Fazi et al, 2005; Fukao et al, 2007; Eyholzer et al, 2009), was confirmed and used as a positive control for the array experiments, with a two-fold induction after restoring CEBPA in our cell line model.

Table 1. miRNAs affected by CEBPA in hematopoietic cells.

			Literature available
miRNA	Chr. locus	Fold change a	Expression b	Regulation c	Targets d	Function e
(A) miRNAs > two-fold decreased after CEBPA restoration
miR-98	Xp11.2	−2.15	↑ Breast, lung cancer (Yan et al, 2008; Bhat-Nakshatri et al, 2009; Du et al, 2009)	↑ After Myc inhibition (Sampson et al, 2007)	FUS1, E2F2, Myc, MGA2 (Hebert et al, 2007; Sampson et al, 2007; Bhat-Nakshatri et al, 2009; Du et al, 2009)	Potentiates doxorubicin, cisplatin resistance (Hebert et al, 2007)
miR-181b  miR-181 family	1q32.1 9q33.3	−2.40	↑ Erythropoiesis (Choong et al, 2007), B-cell differentiation (Chen et al, 2004); ↓ megakaryopoiesis (Garzon et al, 2006) ↑ AML with CEBPA mut (Marcucci et al, 2008); ↓ in ATRA or HNE differentiated leukemic cells (Garzon et al, 2007; Careccia et al, 2009; Pizzimenti et al, 2009), CLL (Pekarsky et al, 2006); ↓ associated to disease progression in CN-AML (Marcucci et al, 2008); ↑↓ various solid tumors (Miller et al, 2008; Wong et al, 2008; Yan et al, 2008; Conti et al, 2009; Ji et al, 2009)	↑ Hypoxia, by HIF1α (Kulshreshtha et al, 2007)	TCL1 (Pekarsky et al, 2006); GATA6, CDX2, NLK (Ji et al, 2009)	↑ B-cell differentiation (Chen et al, 2004), ↓ differentiation in hepatocellular carcinoma (Ji et al, 2009); ↓ proliferation, invasion of glioma (Shi et al, 2008), lung cancer (Cheng et al, 2005), ↑ apoptosis (Shi et al, 2008)
miR-197	1p13.3	−2.26	↑ Various solid tumors (Weber et al, 2006; Wang et al, 2007; Nikiforova et al, 2008; Wong et al, 2008; Du et al, 2009).		FUS1 (Du et al, 2009), ACVR1, TSPAN3 (Weber et al, 2006)	↑ Proliferation (Weber et al, 2006)
miR-210	11p15.5	−2.13	↑ Erythroid differentiation (Bianchi et al, 2009); ↑ in various solid tumors and other diseases (Camps et al, 2008; Foekens et al, 2008; Bimpaki et al, 2009; Cho et al, 2009; Malzkorn et al, 2009; Satzger et al, 2009; Tombol et al, 2009; Jung et al, 2009; Greither et al, 2010)	↑ Hypoxia (Kulshreshtha et al, 2007; Giannakakis et al, 2008; Pulkkinen et al, 2008), by HIF1α (Camps et al, 2008; Pulkkinen et al, 2008)	E2F3 (Giannakakis et al, 2008), MNT (Zhang et al, 2009), RAD52 (Crosby et al, 2009), (Fasanaro et al, 2008)	↑ Cell proliferation (Zhang et al, 2009), angiogenesis, cell migration (Fasanaro et al, 2008); ↓ Pro-apoptotic signaling (Kulshreshtha et al, 2007), DNA repair (Crosby et al, 2009); potential biomarker: detectable in plasma/sera of pancreatic adenocarinoma (Wang et al, 2009), lymphoma patients (Lawrie et al, 2008)
miR-342	14q32.2	−2.16	↑ After ATRA differentiation (Garzon et al, 2007; Careccia et al, 2009; De Marchis et al, 2009), ↑↓ Hematologic diseases (Guglielmelli et al, 2007; Ronchetti et al, 2008), solid tumors (Grady et al, 2008; Miller et al, 2008; Lowery et al, 2009)	↑ By PU.1, IRF-9 (De Marchis et al, 2009), ↓ by PML/RARA, IRF-1(Careccia et al, 2009; De Marchis et al, 2009)		↑ Differentiation (De Marchis et al, 2009) apoptosis (Grady et al, 2008)
miR-432	14q32.3	−2.20
miR-550	7p15.1	−2.18
miR-766	Xq24	−2.59
(B) miRNAs > two-fold increased after CEBPA restoration
miR-29b  miR-29 family	1q32.2 7q32.3	+2.03	↓ AML in general (Garzon et al, 2008), patients with NPM1 mut + lack FLT3-ITD (Garzon et al, 2008), MLL translocations (Garzon et al, 2008; Li et al, 2008), -7q (Garzon et al, 2009); CLL disease progression (Calin et al, 2005; Stamatopoulos et al, 2009; Visone et al, 2009); various solid tumors (Fabbri et al, 2007; Mott et al, 2007; Wang et al, 2008; Xiong et al, 2009)	↓ By Myc (Chang et al, 2008), NFκB, YY1 (Wang et al, 2008)	p85α, CDC42 (Park et al, 2009); Bcl-2, Mcl-1(Mott et al, 2007; Garzon et al, 2009; Xiong et al, 2009); Tcl1 (Pekarsky et al, 2006), YY1 (Wang et al, 2008), CXXC6, CDK6 (Garzon et al, 2009) DNMT3A,B (Fabbri et al, 2007; Garzon et al, 2009)	↑ Differentiation (Wang et al, 2008; Garzon et al, 2009; Li et al, 2009) apoptosis (Mott et al, 2007; Garzon et al, 2009; Park et al, 2009; Xiong et al, 2009); ↓ proliferation (Muniyappa et al, 2009; Xiong et al, 2009), cell migration (Muniyappa et al, 2009), de novo methylation (Fabbri et al, 2007; Garzon et al, 2009)
miR-223	Xq12	+2.02	↑ normal myeloid cells (Chen et al, 2004; Ramkissoon et al, 2006; Johnnidis et al, 2008); ↓ various leukemia types (Debernardi et al, 2007; Mi et al, 2007; Stamatopoulos et al, 2009)	↑ By CEBPA/B (Fazi et al, 2005; Fukao et al, 2007; Eyholzer et al, 2009), ↓ by NFIA (Fazi et al, 2005), AML1-ETO (Fazi et al, 2007)	E2F1(Pulikkan et al, 2009), NFIA (Fazi et al, 2005), LMO2 (Felli et al, 2009)	↑ Differentiation (Fazi et al, 2005; Fazi et al, 2007), maturation, functionality of granulocytes (Johnnidis et al, 2008); ↓ erythroid differentiation (Felli et al, 2009); cell cycle progression (Pulikkan et al, 2009)
miR-370	14q32.3	+3.14	↑ AML with t(15;17) (Dixon-McIver et al, 2008),↓ solid tumors, progression (Haller et al, 2010; Meng et al, 2008)	↓ By IL-7 (Meng et al, 2008)	MAP3K8 (Meng et al, 2008)	↓ Growth of malignant cholangiocytes (Meng et al, 2008)
miR-496	14q32.3	+4.30
miR-572	4p15.3	+3.00
miR-575	4q21.2	+2.82	↓ in HNE differentiated HL60 leukemic cells (Pizzimenti et al, 2009)
miR-630	15q24.1	+4.73
miR-638	19p13.2	+2.12	↑ in senescent fibroblasts (Maes et al, 2009); ↓ ratio miR-92/-638 in AML, ALL (Tanaka et al, 2009)
miR-663	20p11.1	+3.18	↑ in HNE differentiated HL60 leukemic cells (Pizzimenti et al, 2009), senescent fibroblasts (Maes et al, 2009); hypermethylated in breast cancer (Lehmann et al, 2008)
miR-765	1q23.1	+2.02

Abbreviations: AML=acute myeloid leukemia; CEBPA=CCAAT/enhancer-binding protein-α; CLL=chronic lymphoid leukemia; IL=interleukin; miRNA=microRNA; NF κB=nuclear factor κB; NFIA=nuclear factor IA.

References are given in Supplementary Table 3.

^aMean expression change (suppression (−) or induction (+)) out of two miRNA microarray experiments, analyzed with GeneSpring GX 9.0 software.

^bExpression data summarized with ↑ for induction or ↓ suppression of miRNA referenced in literature. For miRNAs with differing expression depending on tissue context, expression is shown as ↑↓.

^cDirect activator ↑ or suppressor ↓ of referenced miRNA.

^dFunctionally tested and verified targets only.

^eEffect of miRNA: on cellular mechanisms induced ↑ or suppressed ↓ by a particular miRNA.

With a focus on haematopoiesis, differentiation, and/or carcinogenesis, we summarised the rapidly increasing literature available for the 18 identified miRNAs in Table 1 (for references see also Supplementary Table S3). Most of these reports describe expression patterns in various types of normal tissues and cancer, whereas reports on the regulation of specific miRNAs are rare.

In this study, we focused on CEBPA-regulated miRNAs with tumour-suppressive functions in haematopoiesis, and miR-29b represented the most prominent candidate. miR-29b belongs to a miRNA family comprising three members (miR-29a, -29b, and -29c), which have been reported to be suppressed in various cancer types (Fabbri et al, 2007; Mott et al, 2007; Wang et al, 2008), including leukaemias (Li et al, 2008; Stamatopoulos et al, 2009; Garzon et al, 2009b). Furthermore, they were shown to induce differentiation (Wang et al, 2008; Li et al, 2009; Garzon et al, 2009b) and apoptosis (Park et al, 2009), and inhibit epigenetic silencing due to de novo methylation (Fabbri et al, 2007; Garzon et al, 2009b).

CEBPA mediates miR-29b expression in AML

We aimed to verify the results of the miRNA microarray by qRT-PCR. We observed that miR-29b was, indeed, induced two-fold after CEBPA restoration in the Kasumi-1-CEBPA-ER cell line system (Figure 1A). We then investigated the effect of CEBPA knock down on miR-29b expression. We used parental U937 leukaemic cells, expressing high levels of endogenous CEBPA as well as a tet-off system conditionally expressing the oncogenic t(8;21) fusion protein AML1-ETO (Pabst et al, 2001a). Induction of AML1-ETO in these cells efficiently blocked CEBPA protein expression (Figure 1B, left), which led to suppressed miR-29b expression (Figure 1B, right).

Figure 1.

CEBPA mediates miR-29b expression in leukaemic cells. (A) Mature miR-29b expression was induced two-fold after restoring CEBPA function in leukemic Kasumi-1 cells. The CEBPA target miR-223 was used as positive control for restored CEBPA function. Results are given as fold expression compared with untreated cells (day 0, ^*P<0.05) and represent three independant experiments. (B) Conditional expression of AML1-ETO abolished CEBPA protein expression in U937 leukemic cells (B, left) and suppressed miR-29b expression (^*P<0.05; B, right). miR-29b expression is given as fold changes compared with the control cells U937-T (ΔΔC_t-method) and represent three independant experiments. (C) Protein levels of the putative miR-29b activator CEBPA and the miR-29b target DNMT3B inversely correlated in leukemic cell lines (C, left). miR-29b expression correlated to CEBPA, and inversely correlated to DNMT3B protein levels (C, right). miR-29b expression is given as ΔC_t-values (C_t(miR-29b)−C_t(normalisation)) representing three independant experiments.

Interestingly, CEBPA-associated expression of miR-29b was further observed across a variety of leukaemic cell lines: the expression of CEBPA protein and miR-29b in HL60, K562, Kasumi-1, and U937 cells inversely correlated to the protein expression of the previously identified miR-29b target gene DNA methyltransferase 3B (DNMT3B, Figure 1C; Fabbri et al, 2007; Garzon et al, 2009b). As DNMT3B is mediating de novo DNA methylation and thus epigenetically inactivates tumour suppressor genes in cancer (Robertson et al, 1999; Rhee et al, 2002; Lin et al, 2007), these observations connect blocked differentiation through CEBPA suppression with deregulated methylation because of the suppressed miR-29b activity.

miR-29b expression is suppressed in AML patients with impaired CEBPA function or with monosomy 7 or del(7q)

To evaluate the importance of CEBPA-mediated miR-29b induction in vivo, we analysed miR-29b expression in diagnostic samples of 66 AML patients, three samples of enriched CD34+ myeloid stem cells, and in samples of mature granulocytes and monocytes from 6 healthy volunteers (Figure 2).

Figure 2.

miR-29b expression in AML patients and healthy controls. miR-29b expression was assessed in samples from 66 AML patients, in three samples of enriched CD34+ myeloid stem cells as well as in mature granulocytes and monocytes from six healthy volunteers. The cohort of consecutive AML samples showed suppressed miR-29b expression compared with granulocytes (P=0.043). Patients with CEBPA deficiency (CEBPA mutations, t(8;21), inv(16)) or chromosome 7q alterations (monosomy 7 or del(7q)) represented roughly one-third of the entire cohort and showed differences in miR-29b expression compared with granulocytes from healthy volunteers (^**P<0.001 for all three subgroups with deficient CEBPA function, and ^*P<0.05 for −7q) as well as compared with the remaining 45 AML patients (wt CEBPA and 7q, ^**P<0.001). miR-29b expression was not suppressed in the remaining 45 patients (wt CEBPA and 7q) if compared with mature granulocytes (P=0.182, NS). Expression levels are given as ΔC_t-values (C_t(miR-29b)−C_t(normalisation)).

We observed that the mean expression of miR-29b was suppressed in the entire cohort of AML patients compared with normal granulocytes (P=0.043). In our cohort, we then separately analysed the patients with suppressed CEBPA function. This group comprised the AML patients with CEBPA mutations, with t(8;21) or with inv(16) (Pabst et al, 2001a, 2001b; Helbling et al, 2005). We found that these AML patients had suppressed miR-29b compared with mature granulocytes (P=0.0001 for CEBPA mutated, P<0.0001 for t(8;21) and inv(16)). Remarkably, the low miR-29b levels were comparable with miR-29b expression in CD34+ precursor cells, which hardly express detectable amounts of CEBPA (Radomska et al, 1998).

In addition, we confirmed previous observations (Garzon et al, 2009a) that miR-29b is suppressed in patients with monosomy 7 or del(7q) (P=0.012). On combining AML patients with alterations of chromosome 7q or CEBPA (n=21), we observed low miR-29b expression compared with the remaining 45 patients of our cohort, with other or no detectable genomic alterations (P=0.0002). We thus confirmed in our cohort of 66 AML patients that miR-29b expression is associated with CEBPA levels and therefore suppressed in patients with disrupted CEBPA function.

Only miR-29a/b1 is induced after restoring CEBPA in human AML cells

miR-29b belongs to the miR-29 family that is encoded in two clusters on two chromosomes (Figure 3A): miR-29a as well as miR-29b on chromosome 7q32.3, and miR-29c as well as, again, miR-29b on chromosome 1q32.2. Mature miR-29b is therefore encoded by two distinct precursor stem sequences (pre-miRNA) on both chromosomes, a pre-miR-29b1 and pre-miR-29b2 stem. Although the sequences of the two pre-miR-29b stems are differing, mature miR-29b resulting from these two stem structures is identical.

Figure 3.

CEBPA activates miR-29b at the pri-miR-29a/b1 locus on chromosome 7q32.3. (A) miR-29b belongs to a family of three members (a, b, c), encoded on two loci on chromosome 1q32.2 and chromosome 7q32.3. Although miR-29b is encoded on both chromosomes, the mature miR-29b sequence encoded from the two loci is identical. (B) In addition to miR-29b, only mature miR-29a is induced after CEBPA restoration, but not mature miR-29c. (C) miR-29 family members are generated from two polymerase II primary transcripts: pri-miR-29a/b1 (GenBank accession number EU154353) and pri-miR-29b2/c (EU154351 and EU154352). These primary transcripts are processed to double stranded precursors (pre-miR-29) and ultimately to the mature single stranded miR-29. Both pri-miR-29s are highly conserved in their putative promoter region and in the pre-miR-29 stem sequences, encoded in the last intron (pre-miR-29a, -b1) on chr.7q32.3 and the last exon (pre-miR-29b2, -c) on chr.1q32.2 respectively. (D) Primer pairs dispersed over the pri-miR-29a/b1 and pri-miR-29b2/c confirmed induction of the pri-miR-29a/b1 locus on chr.7q32.3 (D, left), whereas the pri-miR-29b2/c on chromosome 1.q32.2 is not affected by CEBPA expression (D, right). Results are given as fold expression compared with untreated cells (day 0, ^*P<0.05) and represent three independant experiments.

Consequently, we first investigated the transcriptional effects of CEBPA on the two miR-29 loci to define the individual contribution of each locus to miR-29b expression. Our microarray data indicated a roughly two-fold induction of miR-29a expression after restoring CEBPA in Kasumi-1 cells, whereas miR-29c tended to be suppressed (−1.3-fold). By qRT-PCR, we confirmed that miR-29a was induced two-fold 72 h after CEBPA restoration, similarly to miR-29b. In contrast, the expression of miR-29c was not affected (Figure 3B). This suggests that miR-29a and miR-29b, but not miR-29c, are regulated by CEBPA.

Previous reports (Chang et al, 2008; Wang et al, 2008) indicated that mature miR-29 family members encoded on the same chromosome are processed from a common primary transcript (pri-miRNA, Figure 3C). We thus designed a series of primer pairs dispersed over the pri-miR-29a/b1 and pri-miR-29b2/c sequences. Again, we observed a two-fold induction of pri-miR-29a/b1 (Figure 3D, left), whereas the expression of the miR-29b2/c primary transcript remained stable (Figure 3D, right). This is consistent with the above-mentioned observation of suppressed miR-29b in AML patients with aberrant chromosome 7q. We thus concluded that CEBPA activates the expression of the miR-29a/b1 cluster on chromosome 7, whereas it does not affect miR-29b2/c on chromosome 1 in myeloid leukaemic cells.

CEBPA specifically activates the pri-miR-29a/b1 promoter

As previously shown by RACE experiments (Chang et al, 2008), the primary miR-29a/b1 transcript starts 35.7 kb upstream of the pre-miR-29b1 stem structure, and the highly conserved promoter region just upstream of this transcription start is responsible for regulation of miR-29a/b1 expression (Figure 3C).

A computational analysis of the conserved region spanning −682 bp upstream to +296 bp downstream of the pri-miR-29a/b1 transcription start site indicated six potential CEBP binding sites (Figure 4A). Using luciferase reporter assays, we observed that CEBPA, indeed, activated the entire conserved promoter region two-fold in a dose-dependent manner (Figure 4A). Deletion and mutation constructs of the pri-miR-29a/b1 promoter identified a CEBP binding site located +15 to +29 bp immediately downstream of the transcription start site to be responsible for CEBPA-mediated activation of the pri-miR-29a/b1 promoter (Figure 4B). Chromatin immunoprecipitation assays in myeloid leukaemic cells confirmed that CEBPA is, in fact, binding in vivo to this part of the pri-miR-29a/b1 locus as suggested by the luciferase experiments (Figure 4C): both endogenous CEBPA in U937 cells and exogenous CEBPA in Kasumi-CEBPA-ER were binding to the CEBPA site located +15 to +29 bp downstream of the pri-miR-29a/b1 transcript start.

Figure 4.

CEBPA activates the pri-miR29a/b1 promoter on chromosome 7q32.3. Results represent three independant experiments and are given as fold changes compared with the empty pcDNA3 expression vector; ^*P<0.05, control: empty pGL3b luciferase vector. (A) A computational analysis of the highly conserved region spanning −682 to +296 bp across the pri-miR-29a/b1 transcription start site resulted in six putative CEBPA binding sites. This sequence was cloned into the pGL3b luciferase vector and 200 ng of promoter construct were transfected with 1–10 ng of CEBPA expression plasmid. (B) The CEBPA binding site +15 to +29 bp downstream of the pri-miR-29a/b1 transcription start was identified to be responsible for pri-miR-29a/b1 activation. Deleted (B, upper panel) or mutated (B, lower panel) pri-miR-29a/b1 promoter construct (200 ng) were transfected with 2 ng CEBPA expression plasmid. (C) Chromatin immunoprecipitation (ChIP) assays confirmed binding of CEBPA to the site in the pri-miR-29a/b1 transcription start region. Endogenous CEBPA of U937 cells (C, left) and exogenous CEBPA in Kasumi-1-CEBPA-ER cells (C, right) were binding to the CEBPA site identified by the luciferase assays above. Binding of CEBPA to the regulatory element of pre-miR-223 was used as positive control for these ChIP experiments.

Furthermore, we sought to exclude additional functional CEBPA-binding sites in the non-conserved region directly upstream of the pre-miR29a and -29b1 stem structures. Such additional CEBPA responsive promoter elements were reported for CEBPA regulation of miR-223 (Fazi et al, 2005; Eyholzer et al, 2009) or miR-661 (Reddy et al, 2009). Although the computational sequence analysis of 2.2 kb upstream of the pre-miR-29b1 stem indicated four putative CEBP binding sites, we found that none of them was CEBPA responsive in luciferase assays (data not shown). We thus conclude that CEBPA activates miR-29a/b expression through direct binding to a single site in the conserved promoter region of the pri-miR-29a/b1 transcript on chromosome 7q32.3.

Discussion

The transcription factor CEBPA is a master regulator within normal haematopoiesis (Pabst and Mueller, 2007; Koschmieder et al, 2009). Increasing evidence indicates that CEBPA is exerting its regulatory effects, at least in part, by direct regulation of specific miRNAs. Fazi et al (2005) first identified miR-223 as a direct target of CEBPA. The activation of miR-223 by CEBPA triggers granulocytic differentiation and maturation (Fazi et al, 2005, 2007). Recently, miR-661 was reported to be another direct CEBPA target miRNA. miR-661 suppresses the metastatic tumour antigen 1, a gene broadly upregulated in human cancer (Reddy et al, 2009).

In this study, we sought to identify the pattern of miRNAs that are regulated by CEBPA in haematopoietic cells. Using leukaemic Kasumi-1 cells with conditionally inducible CEBPA function (Pabst et al, 2001a), we determined the expression changes of 470 human miRNAs. We identified 18 miRNAs, whose expression levels were changed more than two-fold after restoring CEBPA function: miR-98, miR-181b, miR-197, miR-210, miR-342, miR-432, miR-550, and miR-776 were suppressed, whereas miR-29b, miR-223, miR-370, miR-496, miR-572, miR-575, miR-630, miR-638, miR-663, and miR-765 were induced compared with their expression levels before CEBPA induction. As expected, the previously identified CEBPA target miR-223 was induced more than two-fold. In contrast, miR-661 levels remained stable in our system of myeloid leukaemic cells. As miR-661 activation by CEBPA was reported to be involved in some solid tumours (Reddy et al, 2009), it may be less important in haematopoietic cells.

So far, two studies described miRNA expression patterns associated with AML patients with CEBPA mutations (Jongen-Lavrencic et al, 2008; Marcucci et al, 2008). In accordance with our observations, miR-181 family members were induced in patients with CEBPA mutations in both studies. Remarkably, however, these authors have not reported other miRNAs detected by our array approach. Possible explanations might be differences in the type of arrays used or differences arising from a comparison of results obtained from CEBPA restoration in a leukaemic cell line (as in this report) vs differing miRNA patterns seen in patients with or without CEBPA mutations.

Among the 18 identified miRNAs in our approach, we decided to dissect the molecular mechanisms involved in CEBPA-dependent regulation of miR-29b based on its increasingly recognised importance for normal haematopoiesis and leukaemogensis. Suppressed miR-29 levels have been shown to be associated with disease progression in chronic lymphoid leukemia patients (Calin et al, 2005; Stamatopoulos et al, 2009; Visone et al, 2009). In AML, miR-29 suppression is associated to translocations involving the MLL oncogene (Li et al, 2008), but it is induced in patients with NPM1 mutations in the absence of FLT3-ITD alterations (Garzon et al, 2008). Consistent with these expression data suggesting tumour-suppressive properties, miR-29 is reported to trigger differentiation (Wang et al, 2008; Garzon et al, 2009b; Li et al, 2009) and apoptosis (Mott et al, 2007; Garzon et al, 2009a; Park et al, 2009; Xiong et al, 2009) in various tissues as well as having anti-invasive and anti-proliferative properties in solid tumours (Muniyappa et al, 2009; Xiong et al, 2009).

Several potential oncogenes have been reported to be silenced by miR-29, such as Tcl1 (Pekarsky et al, 2006), YY1 (Wang et al, 2008), CXXC6, and CDK6 (Garzon et al, 2009a), the p53 upstream inhibitors p85α and CDC42 (Park et al, 2009), and the anti-apoptotic Bcl2 family members Bcl2 and Mcl1 (Mott et al, 2007; Garzon et al, 2009a; Xiong et al, 2009). Importantly, miR-29 family members were also reported to have an important role in preventing epigenetic silencing of tumour suppressors due to de novo methylation in cancer, as they directly suppress DNMT3A and B (Fabbri et al, 2007; Garzon et al, 2009b).

Despite the variety of reported miR-29 downstream effects, little is known so far on how miR-29 expression is regulated itself. Chang et al (2008) first described the conserved promoter regions of both miR-29 family clusters on chromosome 1q32.2 (miR-29b2/c) and chromosome 7q32.3 (miR-29a/b1). They showed that both clusters were suppressed by the oncogenic transcription factor Myc in B-cell lymphoma. Wang et al (2008) proposed that the miR-29b2/c cluster on chromosome 1 is suppressed in rhabdomyosarcoma through NFκB/YY1 via the same conserved upstream promoter region.

In this study, we report that the haematopoietic master transcription factor CEBPA is inducing miR-29b expression. We observed that miR-29b is suppressed in AML patients with disrupted CEBPA function. This comprises AML patients with CEBPA mutations or with suppressed CEBPA function because of t(8,21) or inv(16) chromosome aberrations (Pabst et al, 2001a, 2001b; Helbling et al, 2005). We also confirmed recent observations by others (Garzon et al, 2009a) that miR-29b is suppressed in AML patients with alterations of chromosome 7 (monosomy 7 or del(7q)). Interestingly, functional analysis of CEBPA-mediated miR-29b expression indicated that only the miR-29a/b1 locus on chromosome 7q32.3 is activated by CEBPA, whereas miR-29b2/c expression is not affected by CEBPA. This was surprising as the conserved promoter region upstream of the miR-29b2/c primary transcript on chromosome 1q32.2 (Chang et al, 2008) also indicated several putative CEBPA binding sites in a computational analysis. However, we found that none of them turned out to be functional. The finding that CEBPA induces miR-29b expression only from its chromosome 7q32.3 locus (miR-29a/b1 cluster) provides a rationale for miR-29b suppression observed in patients with alterations of chromosome 7.

In summary, using miRNA microarrays, we found that CEBPA affects the expression of a defined subset of 18 miRNAs in human AML cells. Among them, we identified the miR-29a/b1 cluster encoded on chromosome 7q32.3 to be directly activated by CEBPA. The findings of our study suggest a rationale for miR-29b suppression in AML patients with disrupted CEBPA function or with aberrations on chromosome 7.