Comprehensive transcriptome analysis of mouse embryonic stem cell adipogenesis unravels new processes of adipocyte development
- Nathalie Billon1Email author,
- Raivo Kolde†2, 3,
- Jüri Reimand†2,
- Miguel C Monteiro†1,
- Meelis Kull2, 3,
- Hedi Peterson3, 4,
- Konstantin Tretyakov2,
- Priit Adler4,
- Brigitte Wdziekonski1,
- Jaak Vilo2, 3 and
- Christian Dani1
© Billon et al.; licensee BioMed Central Ltd. 2010
Received: 4 June 2010
Accepted: 3 August 2010
Published: 3 August 2010
The current epidemic of obesity has caused a surge of interest in the study of adipose tissue formation. While major progress has been made in defining the molecular networks that control adipocyte terminal differentiation, the early steps of adipocyte development and the embryonic origin of this lineage remain largely unknown.
Here we performed genome-wide analysis of gene expression during adipogenesis of mouse embryonic stem cells (ESCs). We then pursued comprehensive bioinformatic analyses, including de novo functional annotation and curation of the generated data within the context of biological pathways, to uncover novel biological functions associated with the early steps of adipocyte development. By combining in-depth gene regulation studies and in silico analysis of transcription factor binding site enrichment, we also provide insights into the transcriptional networks that might govern these early steps.
This study supports several biological findings: firstly, adipocyte development in mouse ESCs is coupled to blood vessel morphogenesis and neural development, just as it is during mouse development. Secondly, the early steps of adipocyte formation involve major changes in signaling and transcriptional networks. A large proportion of the transcription factors that we uncovered in mouse ESCs are also expressed in the mouse embryonic mesenchyme and in adipose tissues, demonstrating the power of our approach to probe for genes associated with early developmental processes on a genome-wide scale. Finally, we reveal a plethora of novel candidate genes for adipocyte development and present a unique resource that can be further explored in functional assays.
Obesity has become a major public health problem for industrialized countries. This pathology is associated with an increased risk of metabolic troubles, such as type 2 diabetes, cardiovascular diseases, and certain types of cancers. Obesity is the result of an imbalance between energy intake and expenditure and is often characterized by an increase in both adipocyte size (hypertrophia) and number (hyperplasia). Besides the clinical importance of obesity, we still have limited information regarding the origin and the development of fat tissues.
Adipogenesis is generally described as a two-step process. The first step consists of the generation of committed adipocyte precursors (or preadipocytes) from mesenchymal stem cells (MSCs), while the second step involves the terminal differentiation of these preadipocytes into mature, functional adipocytes. By definition, MSCs are endowed with self-renewal properties and differentiation potentials towards all mesenchymal cell types, while preadipocytes have lost the ability to differentiate into mesenchymal derivatives other than adipocytes. The differentiation of preadipocytes into adipocytes has been extensively studied in vitro using preadipocyte cell lines that were selected from disaggregated mouse embryos or adult adipose tissue for their ability to accumulate cytoplasmic triacylglycerols [1–3]. These cell lines are believed to be faithful models of preadipocyte differentiation and they have provided important insights into the transcriptional control of the late steps of adipogenesis. In contrast, the early steps of adipocyte development remain largely unknown. Although there have been attempts to characterize the distinct cellular intermediates between MSCs and mature adipocytes, such studies have been hampered by the lack of specific cell surface markers to identify and prospectively isolate these cells in vivo. The recent identification and isolation of subpopulations of white adipocyte progenitors in the vasculature of mouse adipose tissues, however, opens new avenues for the understanding of fat cell formation and their modulation in pathological contexts [4, 5].
Until now, knowledge about mesenchymal cell fate decisions has been mostly derived from studies on the immortalized mouse stromal cell line C3H10T1/2, or mesenchymal precursor populations isolated from adult tissues. However, these cellular systems are not informative for the developmental origin of MSCs and adipocytes. Instead, the embryo might constitute a more suitable source of cells to address this issue and elucidate the exact pathways and intermediates between the embryonic stem cell and the mature adipocyte. In particular, mouse embryonic stem cells (mESCs) have provided an invaluable tool to model the earliest steps of adipocyte development in vitro. mESCs are proliferating, pluripotent stem cells that can be propagated indefinitely in vitro in the presence of leukemia inhibitory factor (LIF) [6, 7]. When transplanted into a mouse blastocyst, mESCs integrate into the embryo and contribute to all cell lineages, including germ cells . Similarly, when mESCs are cultured without leukemia inhibitory factor on a non-adherent surface, they aggregate to form embryoid bodies (EBs) containing ectodermal, mesodermal, and endodermal derivatives, thus offering a unique cell culture model to study the earliest steps of mammalian development . Directed differentiation of mESCs towards the adipocyte lineage was first accomplished by Dani et al. , who showed that functional adipocytes could be obtained by exposing EBs to an early and transient treatment with retinoic acid (RA). To dissect out the molecular mechanisms involved in the early steps of adipogenesis, we have recently performed a small-scale drug screening in mESCs using synthetic retinoids as well as pharmacological inhibitors of several signaling pathways . We have demonstrated that retinoic acid receptor β (RARβ) activation is both necessary and sufficient for the commitment of mESCs to the adipocyte lineage. Conversely, pharmacological inhibition of the glycogen synthase kinase 3 (GSK3) completely inhibits RARβ-induced adipogenesis in mESCs, uncovering the requirement of active GSK3 in this process. The induction of mESC differentiation upon single or combined treatment with RARβ agonist and GSK3 inhibitors therefore provides a selective set of screening conditions to uncover the genes involved in the early steps of adipogenesis.
Here, we have used this powerful comparative system to perform a large-scale gene expression profiling of mESC adipogenesis, using a high throughput Affymetrix platform. We then pursued in-depth comprehensive bioinformatics analyses, including de novo functional annotation and curation of the generated data within the context of biological pathways, to unravel several important biological functions associated with the early steps of adipocyte development in mESCs. Finally, we provide a basis for a more comprehensive understanding of how transcriptional regulatory networks might govern these early steps by combining detailed gene regulation studies with in silico analysis of transcription factor (TF) binding sites (TFBSs).
Results and discussion
Large-scale gene expression profiling of mESC adipogenesis
To define genes that are selectively associated with the early steps of adipocyte development in mESCs, we compared the expression levels of CD2314-treated mESCs with those of untreated, Bio- and CD2314+Bio-treated cells at days 6 and 11. We selected only the genes that were either significantly up- or downregulated in CD2314-treated mESCs compared to all three other non-adipogenic conditions. Of the 16,810 genes and expressed sequence tags that are represented on the chips, 500 fulfill these criteria, corresponding to 342 EnsEMBL unique genes. These transcripts were then organized into five clusters that reflect the time when they are differentially expressed during mESC differentiation (Additional file 1). Clusters 1 and 2 contain the genes that are upregulated or downregulated by CD2314 at day 6, respectively; clusters 3 and 4 contain the genes that are upregulated or downregulated by CD2314 at day 11, respectively; and cluster 5 contains genes that are modulated by CD2314 at both day 6 and day 11, and thus encompasses potential candidate genes for both early and later steps of adipocyte development.
We next validated our microarray data by examining the expression levels of 30 representative genes by quantitative real-time PCR (qPCR) in three independent experiments (Additional file 2). These genes encompassed several biological categories, such as cell surface and extracellular matrix components, TFs, and signal transduction and metabolism-associated molecules. As indicated in Additional file 2, the expression profiles of 29 of these genes gave comparable patterns to the microarray analysis, i.e. a validation rate of 96%.
Adipocyte development is associated with several important biological functions in mESCs
Early steps of adipocyte development are coupled to blood vessel formation in mESCs
The first phase of adipogenesis, which begins right after CD2314 exposure (day 6 of differentiation, cluster 1), is characterized by a dramatic enrichment in genes involved in developmental processes, such as organ and anatomical structure development (Figure 2). Among them, many are known to regulate blood vessel morphogenesis, such as angiopoietin 1 (Angpt1), its receptor endothelial-specific receptor tyrosine kinase (Tek), vascular endothelial growth factor C (Vegfc), disintegrin-like and metallopeptidase with thrombospondin type 1 motif 1 (Adamts1) and the TF forkhead box C2 (Foxc2). A close spatial and temporal relationship between adipocyte and blood vessel formation exists during fetal development. Blood vessels and first formed adipocytes appear coincidentally and are always found in close association in vivo, so that a common precursor for adipocytes and endothelial cells has been suggested, although never formally isolated [14–16]. The prevalence of vasculature-associated genes in CD2314-regulated cluster 1 suggests that, similarly to normal development, the early steps of adipocyte formation in mESCs are coupled to blood vessel morphogenesis. Interestingly, an elegant genetic lineage-mapping study recently shed new light on the interplay between the adipocyte and the endothelial lineages by showing that white adipocyte progenitors reside in the mural compartment of the adipose vasculature in mice . The observation that the mESC culture system might allow the development of both adipose cells and their potential vascular niche opens exciting perspectives for the prospective isolation and the biochemical characterization of these newly identified adipocyte progenitors by offering an abundant source for these cells.
Early steps of adipocyte development are coupled to neural development in mESCs
Another striking observation that arises from the functional annotations of both clusters 1 and 5 (Figure 2) is the enrichment in neural development-associated genes at both day 6 and day 11 of mESC adipogenesis. This group includes genes like the neurotrophin receptors neurotrophic tyrosine kinase, receptor, type 2 (Ntrk2) and nerve growth factor receptor (ngfr) , roundabout homolog (robo2) , the TFs hairy and enhancer of split 5 (Hes5)  and paired box gene 6 (Pax6) , which are all known to play important functions in the control of mammalian neurogenesis and axon guidance. Interestingly, this group also contains genes involved in the development of the neural crest, such as homeobox A2 (Hoxa2) , paired-like homeobox 2b (Phox2B) , semaphorin 3 D (Sema3D)  and endothelin receptor type B (Ednrb)  (indicated by an asterisk in Figure 2). The neural crest comprises a transient cell population of vertebrate embryos that generates the peripheral nervous system, pigment cells, most of the craniofacial skeleton, as well as other derivatives . These data indicate that the early steps of adipocyte formation might be closely associated with nervous system/neural crest development. In accordance with these findings, we have demonstrated that, during normal mouse development, a subset of adipocytes in the cranial region of the body is generated by the neural crest, rather than by mesodermal progenitors, classically thought to be at the origin of this lineage . Furthermore, we have shown that adipocytes obtained from mESCs upon RA treatment are mostly derived from the neuroectoderm and that this phenomenon is associated with a precocious upregulation of neural crest markers . The neural origin of adipocytes generated by embryonic stem cells exposed to RA has been confirmed by Takashima et al. , who also used an elegant approach to demonstrate that the earliest wave of MSC production in the mouse embryo is generated from the neuroepithelium, and not the mesoderm. The results presented here corroborate these findings and indicate that genomics data can be successively mined to unravel plausible biological functions. They further indicate that RARβ might mediate RA effects on neural and adipocyte development in mESCs.
Early steps of adipocyte development involve major changes in cell signaling components: analysis of the Wnt pathway
To clarify the role of sFRPs in the early steps of adipocyte development, we assessed the effect of exogenous addition of sFRP-1 on differentiating mESCs. To measure Wnt pathway activity, we used mESCs stably transfected with the TOP-FLASH reporter construct, which contains the Firefly luciferase reporter gene under the control of TCF/LEF (T-cell-specific transcription factor/lymphoid enhancer binding factor) response elements (TCF/LEF being the main transcriptional effectors of the Wnt pathway). As expected, sFRP-1 addition between days 3 and 6 of EB formation inhibited Wnt pathway activity (Figure 4b). However, sFRP-1 addition, alone or in combination with CD2314, had no significant effect on adipocyte formation, GPDH activity, or the expression of adipocyte-differentiation markers (Figure 4c-e). Therefore, inhibiting the Wnt pathway activity through addition of exogenous sFRP-1 was not sufficient to drive adipocyte development in mESCs. In accordance with other recent observations, these results suggest that although RARβ and active GSK3 are required for adipocyte formation in mESCs, they are likely to be acting through a Wnt pathway-independent mechanism .
In silicogene regulation analysis provides a basis for the understanding of transcriptional control of adipocyte development
The differentiation of preadipocytes into adipocytes is regulated by an extensive network of TFs that coordinate the expression of several genes essential for the acquisition of mature fat-cell characteristics. Among them, Peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT-enhancer-binding proteins (C/EBPs) are considered as master regulators of the entire terminal differentiation process (for a review, see ). In contrast, the transcriptional processes controlling the conversion of mesenchymal precursors to preadipocytes are largely unknown. To provide a basis for a more comprehensive understanding of how transcriptional control governs these early steps in mESCs, we used a combination of computational and experimental approaches.
Analysis of the expression of TFs associated with mESC adipogenesis during mouse embryogenesis and in mouse adipose tissues
In addition to TFs known to participate in adipogenesis and adipose function, we also identified several TFs with no previous link to adipocyte biology. To assess the relevance of the TFs differentially expressed in mESCs for mesenchymal and adipocyte formation during normal development, we used the Mouse Genome Informatics (MGI) web tool, together with extensive literature curation, to analyze the reported expression of such TFs during mouse embryogenesis. In particular, we had a closer look at mesenchymal tissues, since the adipocyte lineage originates from mesenchymal precursors. As reported in Figure 5, a large proportion (77%) of the TFs present in clusters 1 to 5 were detected in mesenchymal compartments between day 7 and day 18.5 of mouse embryonic development. Interestingly, some of them (23%) were specifically associated with neural crest-derived mesenchyme, again suggesting that adipocytes developing from mESCs do so, at least in part, through a neural crest pathway.
In silicoanalysis of TFBS enrichment in CD2314-modulated clusters
Some of the enriched motifs highlighted by our analysis bind to TFs already known to exert a pro-adipogenic effect in various cellular models of adipocyte differentiation. For instance, Leukemia/lymphoma-related factor (LRF) has been show to be expressed in human and mouse adipocyte precursors, where it might promote differentiation by blocking cell cycle progression . Similarly, Early growth response protein-2 (EGR2, or KROX20), is induced early during 3T3-L1 adipogenesis and promotes C/EBPβ expression, while decreasing its expression reduces the ability of these cells to differentiate . Finally, C/EBP family members act as master regulators of adipocyte differentiation both in vitro and in vivo . Together, these data suggest that TFBS enrichment analysis may constitute a very useful approach to unravel new transcriptional networks involved in the early steps of mESC adipogenesis.
Besides binding sites for TFs known to participate in adipogenesis, we also identified several motifs that suggested novel factors in adipocyte biology. For instance, the genes associated with adipocyte development in mESCs were enriched for a motif bound by three members of the Activator protein 2 (AP-2) family of TFs . In mice, these TF genes (AP-2α, AP-2β and AP-2γ) are co-expressed in neural crest cells, the peripheral nervous system, as well as facial and limb mesenchyme, where they play crucial roles during development [18, 48]. Mutation of AP-2α predominantly affects the cranial neural crest and the limb mesenchyme, leading to profound disturbances of facial and limb development. Together, these data place the AP-2 family members as interesting candidates for the regulation of adipocyte generation through the neural crest developmental pathway, which has been shown to account for the generation of cephalic WAT in mouse .
Finally, we performed an integrated study compiling TFBS enrichment results, gene expression profiling and PPI analysis. Interestingly, three motifs enriched in cluster 3 (day 11) correspond to binding sites for TFs upregulated at day 6 of mESC adipogenesis (indicated by a star in Figure 7): Cartilage homeo protein 1 (CART-1), Paired related homeobox 2 (PRRX2), and myeloid ecotropic viral integration site 1 (MEIS1) (Figure 5). As revealed by our PPI analysis (Figure 3), MEIS1 physically interacts with HOXB4, HOXA2 and Pre B-cell leukemia transcription factor 1 (PBX1) in a large transcriptional network also involving PAX6 and homeodomain interacting protein kinase 2 (HIPK2), and all these regulators exhibit transcriptional upregulation at day 6 of adipogenesis. To rule out the possibility that this predictive candidate regulatory network might represent a 'noisy artifact' from our transcriptomic study, we examined the expression of its components during mESC adipogenesis at the protein level. As shown in Additional file 3, the interacting partners of this regulatory network could all be detected by western blot in the mESC system. Interestingly, most of them showed the predicted, specific upregulation at day 6 of adipocyte development. In addition, MEIS1, PBX1 and HOXB4 were also upregulated at day 11 of adipocyte development, when enrichment in TFBSs for MEIS1 could be predicted from our in silico analysis, reinforcing the idea that the integrated approach presented here could be very useful to unravel important novel regulators of adipocyte development. Several biochemical and genetic approaches have shown that MEIS1, PBX1 and HOX factors associate in trimeric, DNA-binding transcriptional complexes to modulate gene expression during early embryonic development and organogenesis [49, 50]. Additional studies should now explore the precise role of this network in regulating the early steps of adipocyte commitment.
In the present study, we have used a unique cell model and genome-wide analysis of gene expression to uncover the signaling and transcriptional networks underlying the early steps of adipocyte development, a process that remains largely unknown. Although expression profiling using microarrays has been reported for different adipocyte cell models, no such study aiming at uncovering the early steps of adipocyte formation in mESCs had been conducted so far . Our comprehensive and unbiased approach resulted in the identification of 500 transcripts differentially expressed during mESC adipogenesis, a large proportion of which had no previous link to adipocyte biology. Therefore, these results considerably increase existing knowledge of adipocyte development. Besides providing an unprecedented look at transcriptional changes over the course of adipocyte development in mESCs, our study supports several important biological findings.
First, adipocyte development in mESCs is coupled to blood vessel morphogenesis and neural development, closely mimicking normal mouse development. The observation that the mESC culture system might not only allow the generation of adipose stem cells, but also of their potential vascular niche, opens new avenues for the study of adipose stem cell biology and their close relationship with the endothelial lineage.
Second, the early steps of adipocyte formation involve important changes in cell signaling, including components of the Wnt pathway. Of these, we have further investigated the role of a single candidate, sFRP-1. Functional validation studies provided evidence that this factor is not sufficient to drive adipocyte commitment in the mESC system, suggesting that more complex regulatory mechanisms are needed to allow immature stem cells to launch adipocyte lineage-specific differentiation programs.
Third, adipocyte development in mESCs is regulated by an extensive network of TFs, which might coordinate the expression of genes essential for the acquisition of mesenchymal and adipocyte characteristics. By combining computational and experimental approaches, we show here that a large proportion of these TFs are also expressed in mesenchymal areas during mouse embryogenesis and in mouse adipose tissues, therefore demonstrating the power of our system to probe for genes associated with early developmental processes on a genome-wide scale. In addition, using in silico analysis of the promoters of co-expressed genes, we uncover further putative transcriptional networks that could drive these coordinated gene expression programs.
Finally, we reveal a plethora of novel candidate genes for adipocyte development, and present a unique and comprehensive resource that can be further explored in functional assays.
Materials and methods
mESC culture and induction of adipocyte development
CGR8 mESCs  were used in this study and were propagated as previously described [10, 53]. For EB formation, mESCs were cultivated in aggregates as previously described [10, 53]. From days 3 to 6, EBs were incubated in control medium alone or in the presence of either the RARβ-selective agonist CD2314, the inhibitor of the glycogen synthase kinase (2'Z,3'E)-6-bromoindirubin-3'-oxime (BIO) or both compounds, as previously described . At day 6, EBs were allowed to settle onto gelatin-coated plates. From day 7 onward, EB outgrowths were cultured in the presence of 85 nM bovine insulin, 2 nM triiodothyronine, and 0.5 μM rosiglitazone (BRL4953), a PPARγ agonist. Media were changed every 2 days until day 21. CD2314 was kindly provided by Professor Pierre Chambon (IGBMC; Illkirch, France) and rosiglitazone was a gift of GlaxoSmithKline, Marly le Roy, France. The remaining compounds were bought from Sigma-Aldrich, Lyon, France. For sFRP experiments, differentiating EBs were treated with 100 ng/ml of recombinant sFRP-1 (R&D Systems, Lille, France) daily from days 3 to 6.
Assessment of adipocyte differentiation
Lipid droplets were visualized after Oil Red O staining as described previously [10, 53]. Enzymatic activity of GPDH, an adipocyte-specific enzyme, was measured as previously described . Expression of adipocyte differentiation markers such as Fabp4 and Lpl was measured using qPCR as described below.
White adipose tissue isolation and fractionation
Periepidymal WAT was obtained from 10-week-old C57Bl/6J male mice in accordance with the French and European regulations for the care and use of research animals. Adipose tissues were digested using collagenase (300 U/ml in phosphate-buffered saline, 2% bovine serum albumin, pH 7.4) for 45 minutes under constant shaking. Following removal of the floating mature AF, the lower layer containing the SVF was successively filtrated through 100, 70, and 40 μm sieves, centrifuged (200g, 10 minutes) and resuspended in erythrocyte lysis buffer (Sigma) for 1 minutes. SVF cells were then resuspended in phosphate-buffered saline/2% fetal calf serum and processed for RNA extraction together with the AF.
Microarray experimental design, RNA isolation and microarray hybridization
Samples were generated from mESCs before (day 3) or immediately after (day 6) exposure to control medium, CD2314, BIO, or CD2314+BIO. Samples were also taken at day 11 after exposure to these four conditions. A summary scheme of this strategy is given in Additional file 1. The total number of experimental conditions was then nine, each performed in three separate biological repeats. Total RNA from embryonic stem cells or their derivatives was isolated using the RNeasy Mini Kit from Qiagen (Courtaboeuf, France) and treated with RNase-free DNase I (5 U/100 μg of nucleic acids, Sigma). Biotinylated cRNA was prepared according to the standard Affymetrix protocol. In brief, double-stranded cDNA was synthesized from 10 μg total RNA using the SuperScript Choice System from Invitrogen (Cergy Pontoise, France) and the Affymetrix T7-(dT)24 primer, which contains a T7 RNA polymerase promoter attached to a poly-dT sequence. Following a phenol/chloroform extraction and ethanol precipitation, the cDNA was transcribed into biotin-labeled cRNA using the Retic Lysate IVT™ kit (Ambion Inc., Woodward Austin, TX, USA). cRNA products were purified using the RNeasy kit (Qiagen) and fragmented to an average size of 30 to 50 bases according to Affymetrix recommendations. Fragmented cRNA (15 μg) was used to hybridize the Mouse Genome 430 2.0 Array for 16 hours at 45°C. The arrays were washed and stained in the Affymetrix Fluidics Station 400 and scanned using the Hewlett-Packard GeneArray Scanner G2500A. Image data were analyzed with the GeneChip® Operating Software (GCOS) using Affymetrix default analysis settings. After quality control tests, arrays were normalized by the log scale robust multi-array analysis . The raw data can be obtained from ArrayExpress (accession number [E-TABM-668]).
To identify genes that display a CD2314-specific expression profile, we performed t-tests with each other condition on the same time point. The final clusters are composed of genes that were either up- or downregulated significantly in all comparisons. We used false discovery rate (P = 0.05) as the significance threshold in each of the tests. The statistical analysis was performed using the Limma package from Bioconductor .
All biological quantification data are shown as mean values ± standard error of the mean of at least three independent experiments and tested statistically using two-tailed Student's t-test or Z-test for location, unless otherwise indicated.
Functional annotations, protein-protein interactions, and pathway animations
For functional annotations of selected groups of genes, we used the recently developed g:Profiler web toolkit . To assess PPIs in selected clusters, we downloaded the manually curated collection of human PPIs from the Human Protein Reference Database . Corresponding mouse proteins were retrieved with the g:Orth tool . We used a conservative strategy to map orthologs and only accounted for interactions where both interacting proteins in human had exactly one corresponding protein in mouse. The PPIs in our clusters were extracted with the GraphWeb tool  by setting the input to the Human Protein Reference Database interactions and the Network Neighbourhood to the list of differentially expressed genes of a selected cluster (distance = 0). To better visualize dynamic changes in entire genetic and signaling cellular circuits, we used the KEGGanim web toolkit , which involves a set of animations based on pathways from KEGG .
In silicoprediction analysis of transcription factor binding sites
To predict TFs potentially involved in mESC adipogenesis, we performed in silico analysis of TFBSs in the promoter sequences of CD2314-modulated genes (clusters 1 to 5). Because sequence-specific TFs show a marked increase in binding across the region that encompasses each transcription start site , we focused our analysis on the 2,000 bp upstream and 1,000 bp downstream of each transcription start site. We used the UCSC genome database (mm8 release) to extract these sequences, with transcription start site defined by track RefSeq genes [59, 60]. In case several promoters had more than 1,500 bp overlapping, we randomly discarded all but one of the promoters. In the obtained promoters, we searched for TFBS enrichment, for example, TFBSs that were occurring more often than expected from the comparison with all other mouse gene promoters. For the source of TFBSs, we used the position weight matrices from the TRANSFAC (version 11.4)  and JASPAR  databases. As the first step of the analysis, each position weight matrix was scored in every promoter by taking the highest scoring hit within the promoter using the Storm software . While scanning the promoter for the best match, we only considered the regions that are conserved according to the UCSC Euarchontoglires conservation track. For conservation, we used four different thresholds (0.7, 0.8, 0.9 and 1.0) plus we also performed the analysis with no conservation required. In the latter case, each promoter was scored by averaging the three highest scoring hits in the promoter, instead of a single hit. For both clusters 1 and 3, a position weight matrix was considered interesting if the proportion of promoters scoring over some threshold was significantly higher in the promoters of this list than among all other mouse promoters. The threshold was optimized for the fold-change in the proportion, while requiring the Bonferroni-corrected hypergeometric P-value to be below 0.01. We discarded the results with fold-change less than 1.8 times.
Total RNA was extracted using TRI-Reagent™ kit (Euromedex, Souffelweyersheim, France) according to the manufacturer's instructions and RT-PCR analysis was conducted as described previously. All primers sequences are detailed in Additional file 4. For qPCR, the final reaction volume was 25 μl, including specific primers (0.4 μM), 10 ng of reverse transcribed RNA and 12.5 μl SYBR green master mix (Eurogentec, Angers, France) qPCR conditions were as follows: 2 minutes at 50°C, 10 minutes at 95°C, followed by 40 cycles of 15 s at 95°C, 1 minute at 60°C. Real-time PCR assays were run on an ABI Prism 7700 real-time PCR machine (PerkinElmer Life Sciences, Courtaboeuf, France). Relative gene expression was calculated by the dCT method and normalized to the geometric mean of the expression of three reference genes (βactin, gapdh and tbp).
fatty acid binding protein 4
forkhead box C2
glycogen synthase kinase
homeodomain interacting protein kinase
Kyoto Encyclopedia of Genes and Genomes
myeloid ecotropic viral integration site 1
mouse embryonic stem cell
mesenchymal stem cell
paired box gene 6
Pre B-cell leukemia transcription factor 1
Peroxisome proliferator-activated receptor γ
quantitative real-time PCR
retinoic acid receptor
secreted frizzled-related protein
stromal vascular fraction
transcription factor binding site
white adipose tissue
wingless-related MMTV integration site.
This research was supported by CNRS and by funding under the Sixth Research Framework Programme of the European Union, Project FunGenES (LSHG-CT-2003-503494), the Egide Parrot PHC Programme N° 20679QJ, ERDF through EXCS and the Estonian Science Foundation ETF7437. RK acknowledges the Tiger University Program of the Estonian Information Technology Foundation. JR acknowledges Ustus Agur and Artur Lind foundations for fellowships. MCM was supported by the 'International PhD Program in Developmental and Cellular Decisions' of the University of Nice, an Early Stage Research Training Host Fellowship action of the European Union Marie Curie program and the Portuguese Foundation for Science and Technology.
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