Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor

被引:48
作者
Conboy, Caitlin M. [1 ]
Spyrou, Christiana [1 ,2 ]
Thorne, Natalie P. [1 ,3 ]
Wade, Elizabeth J. [4 ]
Barbosa-Morais, Nuno L. [1 ]
Wilson, Michael D. [1 ]
Bhattacharjee, Arindam [5 ]
Young, Richard A. [6 ,7 ]
Tavare, Simon [1 ,3 ]
Lees, Jacqueline A. [6 ]
Odom, Duncan T. [1 ]
机构
[1] Canc Res UK Cambridge Res Inst, Li Ka Shing Ctr, Cambridge, England
[2] Univ Cambridge, Stat Lab, Dept Pure Math & Math Stat, Cambridge CB2 1SB, England
[3] Univ Cambridge, Dept Appl Math & Theoret Phys, Cambridge CB3 9EW, England
[4] Univ Connecticut, Dept Ecol & Evolutionary Biol, Storrs, CT 06269 USA
[5] Agilent Technol, Andover, MA USA
[6] MIT, Dept Biol, Cambridge, MA USA
[7] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1371/journal.pone.0001061
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Maintaining quiescent cells in G0 phase is achieved in part through the multiprotein subunit complex known as DREAM, and in human cell lines the transcription factor E2F4 directs this complex to its cell cycle targets. We found that E2F4 binds a highly overlapping set of human genes among three diverse primary tissues and an asynchronous cell line, which suggests that tissue-specific binding partners and chromatin structure have minimal influence on E2F4 targeting. To investigate the conservation of these transcription factor binding events, we identified the mouse genes bound by E2f4 in seven primary mouse tissues and a cell line. E2f4 bound a set of mouse genes that was common among mouse tissues, but largely distinct from the genes bound in human. The evolutionarily conserved set of E2F4 bound genes is highly enriched for functionally relevant regulatory interactions important for maintaining cellular quiescence. In contrast, we found minimal mRNA expression perturbations in this core set of E2f4 bound genes in the liver, kidney, and testes of E2f4 null mice. Thus, the regulatory mechanisms maintaining quiescence are robust even to complete loss of conserved transcription factor binding events.
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页数:9
相关论文
共 44 条
[1]
Role for a Drosophila Myb-containing protein complex in site-specific DNA replication [J].
Beall, EL ;
Manak, JR ;
Zhou, S ;
Bell, M ;
Lipsick, JS ;
Botchan, MR .
NATURE, 2002, 420 (6917) :833-837
[2]
GOstat: find statistically overrepresented Gene Ontologies within a group of genes [J].
Beissbarth, T ;
Speed, TP .
BIOINFORMATICS, 2004, 20 (09) :1464-1465
[3]
CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[4]
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
[5]
BOLSTAD B, 2005, QUALITY ASSESSMENT A
[6]
BOLSTAD B, 2007, AFFYPLM METHODS FITT
[7]
A common set of gene regulatory networks links metabolism and growth inhibition [J].
Cam, H ;
Balciunaite, E ;
Blais, A ;
Spektor, A ;
Scarpulla, RC ;
Young, R ;
Kluger, Y ;
Dynlacht, BD .
MOLECULAR CELL, 2004, 16 (03) :399-411
[8]
Emerging roles for E2F: Beyond the G1/S transition and DNA replication [J].
Cam, H ;
Dynlacht, BD .
CANCER CELL, 2003, 3 (04) :311-316
[9]
Identification and classification of genes that act antagonistically to let-60 Ras signaling in Caenorhabditis elegans vulval development [J].
Ceol, Craig J. ;
Stegmeier, Frank ;
Harrison, Melissa M. ;
Horvitz, H. Robert .
GENETICS, 2006, 173 (02) :709-726
[10]
The E2F transcriptional network: old acquaintances with new faces [J].
Dimova, DK ;
Dyson, NJ .
ONCOGENE, 2005, 24 (17) :2810-2826