Comprehensive transcriptome analysis of mouse embryonic stem cell adipogenesis unravels new processes of adipocyte development

被引:25
作者
Billon, Nathalie [1 ]
Kolde, Raivo [2 ,3 ]
Reimand, Jueri [2 ]
Monteiro, Miguel C. [1 ]
Kull, Meelis [2 ,3 ]
Peterson, Hedi [3 ,4 ]
Tretyakov, Konstantin [2 ]
Adler, Priit [4 ]
Wdziekonski, Brigitte [1 ]
Vilo, Jaak [2 ,3 ]
Dani, Christian [1 ]
机构
[1] Univ Nice Sophia Antipolis, Inst Biol Dev & Canc, CNRS UMR 6543, Fac Med Pasteur, F-06108 Nice 2, France
[2] Univ Tartu, Inst Comp Sci, EE-50409 Tartu, Estonia
[3] Quretec, EE-51003 Tartu, Estonia
[4] Univ Tartu, Inst Mol & Cell Biol, EE-51010 Tartu, Estonia
来源
GENOME BIOLOGY | 2010年 / 11卷 / 08期
关键词
GENOME BROWSER DATABASE; GENE-EXPRESSION; FACTOR-II; DIFFERENTIATION; INSULIN; BINDING; BETA; LINE; IDENTIFICATION; PLASTICITY;
D O I
10.1186/gb-2010-11-8-r80
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: 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. Results: 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. Conclusions: 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.
引用
收藏
页数:16
相关论文
共 62 条
[1]   KEGGanim:: pathway animations for high-throughput data [J].
Adler, Priit ;
Reimand, Jueri ;
Jaenes, Juergen ;
Kolde, Raivo ;
Peterson, Hedi ;
Vilo, Jaak .
BIOINFORMATICS, 2008, 24 (04) :588-590
[2]   Nonhematopoietic/endothelial SSEA-1+ cells define the most primitive progenitors in the adult murine bone marrow mesenchymal compartment [J].
Anjos-Afonso, Fernando ;
Bonnet, Dominique .
BLOOD, 2007, 109 (03) :1298-1306
[3]   Semaphorin 3d promotes cell proliferation and neural crest cell development downstream of TCF in the zebrafish hindbrain [J].
Berndt, Jason D. ;
Halloran, Mary C. .
DEVELOPMENT, 2006, 133 (20) :3983-3992
[4]   The generation of adipocytes by the neural crest [J].
Billon, Nathalie ;
Iannarelli, Palma ;
Monteiro, Miguel Caetano ;
Glavieux-Pardanaud, Corinne ;
Richardson, William D. ;
Kessaris, Nicoletta ;
Dani, Christian ;
Dupin, Elisabeth .
DEVELOPMENT, 2007, 134 (12) :2283-2292
[5]   Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project [J].
Birney, Ewan ;
Stamatoyannopoulos, John A. ;
Dutta, Anindya ;
Guigo, Roderic ;
Gingeras, Thomas R. ;
Margulies, Elliott H. ;
Weng, Zhiping ;
Snyder, Michael ;
Dermitzakis, Emmanouil T. ;
Stamatoyannopoulos, John A. ;
Thurman, Robert E. ;
Kuehn, Michael S. ;
Taylor, Christopher M. ;
Neph, Shane ;
Koch, Christoph M. ;
Asthana, Saurabh ;
Malhotra, Ankit ;
Adzhubei, Ivan ;
Greenbaum, Jason A. ;
Andrews, Robert M. ;
Flicek, Paul ;
Boyle, Patrick J. ;
Cao, Hua ;
Carter, Nigel P. ;
Clelland, Gayle K. ;
Davis, Sean ;
Day, Nathan ;
Dhami, Pawandeep ;
Dillon, Shane C. ;
Dorschner, Michael O. ;
Fiegler, Heike ;
Giresi, Paul G. ;
Goldy, Jeff ;
Hawrylycz, Michael ;
Haydock, Andrew ;
Humbert, Richard ;
James, Keith D. ;
Johnson, Brett E. ;
Johnson, Ericka M. ;
Frum, Tristan T. ;
Rosenzweig, Elizabeth R. ;
Karnani, Neerja ;
Lee, Kirsten ;
Lefebvre, Gregory C. ;
Navas, Patrick A. ;
Neri, Fidencio ;
Parker, Stephen C. J. ;
Sabo, Peter J. ;
Sandstrom, Richard ;
Shafer, Anthony .
NATURE, 2007, 447 (7146) :799-816
[6]   The Wnt antagonist secreted frizzled-related protein-1 is a negative regulator of trabecular bone formation in adult mice [J].
Bodine, PVN ;
Zhao, WG ;
Kharode, YP ;
Bex, FJ ;
Lambert, AJ ;
Goad, MB ;
Gaur, T ;
Stein, GS ;
Lian, JB ;
Komm, BS .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (05) :1222-1237
[7]   FORMATION OF GERM-LINE CHIMERAS FROM EMBRYO-DERIVED TERATOCARCINOMA CELL-LINES [J].
BRADLEY, A ;
EVANS, M ;
KAUFMAN, MH ;
ROBERTSON, E .
NATURE, 1984, 309 (5965) :255-256
[8]   Inhibitors of preadipocyte differentiation induce COUP-TF binding to a PPAR/RXR binding sequence [J].
Brodie, AE ;
Manning, VA ;
Hu, CY .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 228 (03) :655-661
[9]   HOX gene network is involved in the transcriptional regulation of in vivo human adipogenesis [J].
Cantile, M ;
Procino, A ;
D'Armiento, M ;
Cindolo, L ;
Cillo, C .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 194 (02) :225-236
[10]   FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance [J].
Cederberg, A ;
Gronning, LM ;
Ahrén, B ;
Taskén, K ;
Carlsson, P ;
Enerbäck, S .
CELL, 2001, 106 (05) :563-573