Genome-wide analysis of FOXO3 mediated transcription regulation through RNA polymerase II profiling

被引:100
作者
Eijkelenboom, Astrid [1 ]
Mokry, Michal [2 ,3 ]
de Wit, Elzo [2 ,3 ]
Smits, Lydia M. [1 ]
Polderman, Paulien E. [1 ]
van Triest, Miranda H. [1 ]
van Boxtel, Ruben [4 ]
Schulze, Almut [5 ]
de Laat, Wouter [2 ,3 ]
Cuppen, Edwin [2 ,3 ]
Burgering, Boudewijn M. T. [1 ]
机构
[1] Univ Med Ctr, Dept Mol Canc Res, NL-3584 CG Utrecht, Netherlands
[2] KNAW, Hubrecht Inst Dev Biol & Stem Cell Res, Utrecht, Netherlands
[3] Univ Med Ctr, NL-3584 CG Utrecht, Netherlands
[4] Univ Med Ctr, Dept Cell Biol, NL-3584 CG Utrecht, Netherlands
[5] Canc Res UK London Res Inst, Gene Express Anal Lab, London, England
关键词
enhancer; FOXO; initiation; RNA pol II; transcription; DNA-BINDING; HISTONE MODIFICATIONS; DOWN-REGULATION; GENE; INSULIN; STRESS; EXPRESSION; CELLS; MYC; IDENTIFICATION;
D O I
10.1038/msb.2012.74
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Forkhead box O (FOXO) transcription factors are key players in diverse cellular processes affecting tumorigenesis, stem cell maintenance and lifespan. To gain insight into the mechanisms of FOXO-regulated target gene expression, we studied genome-wide effects of FOXO3 activation. Profiling RNA polymerase II changes shows that FOXO3 regulates gene expression through transcription initiation. Correlative analysis of FOXO3 and RNA polymerase II ChIP-seq profiles demonstrates FOXO3 to act as a transcriptional activator. Furthermore, this analysis reveals a significant part of FOXO3 gene regulation proceeds through enhancer regions. FOXO3 binds to pre-existing enhancers and further activates these enhancers as shown by changes in histone acetylation and RNA polymerase II recruitment. In addition, FOXO3-mediated enhancer activation correlates with regulation of adjacent genes and pre-existence of chromatin loops between FOXO3 bound enhancers and target genes. Combined, our data elucidate how FOXOs regulate gene transcription and provide insight into mechanisms by which FOXOs can induce different gene expression programs depending on chromatin architecture. Molecular Systems Biology 9: 638; published online 22 January 2013; doi:10.1038/msb.2012.74
引用
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页数:15
相关论文
共 87 条
[21]   FoxO1 regulates Tlr4 inflammatory pathway signalling in macrophages [J].
Fan, WuQiang ;
Morinaga, Hidetaka ;
Kim, Jane J. ;
Bae, Eunju ;
Spann, Nathanael J. ;
Heinz, Sven ;
Glass, Christopher K. ;
Olefsky, Jerrold M. .
EMBO JOURNAL, 2010, 29 (24) :4223-4236
[22]   FOXO3a regulates reactive oxygen metabolism by inhibiting mitochondrial gene expression [J].
Ferber, E. C. ;
Peck, B. ;
Delpuech, O. ;
Bell, G. P. ;
East, P. ;
Schulze, A. .
CELL DEATH AND DIFFERENTIATION, 2012, 19 (06) :968-979
[23]   Identification of the differential distribution patterns of mRNAs and consensus binding sequences for mouse DAF-16 homologues [J].
Furuyama, T ;
Nakazawa, T ;
Nakano, I ;
Mori, N .
BIOCHEMICAL JOURNAL, 2000, 349 :629-634
[24]   Quantifying similarity between motifs [J].
Gupta, Shobhit ;
Stamatoyannopoulos, John A. ;
Bailey, Timothy L. ;
Noble, William Stafford .
GENOME BIOLOGY, 2007, 8 (02)
[25]   Acetylation curtails nucleosome binding, not stable nucleosome remodeling, by FoxO1 [J].
Hatta, M. ;
Liu, F. ;
Cirillo, L. A. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 379 (04) :1005-1008
[26]   Chromatin opening and stable perturbation of core histone: DNA contacts by FoxO1 [J].
Hatta, Mitsutoki ;
Cirillo, Lisa Ann .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (49) :35583-35593
[27]   Genome-wide pattern of TCF7L2/TCF4 chromatin occupancy in colorectal cancer cells [J].
Hatzis, Pantelis ;
van der Flier, Laurens G. ;
van Driel, Marc A. ;
Guryev, Victor ;
Nielsen, Fiona ;
Denissov, Sergei ;
Nijman, Isaac J. ;
Koster, Jan ;
Santo, Evan E. ;
Welboren, Willem ;
Versteeg, Rogier ;
Cuppen, Edwin ;
van de Wetering, Marc ;
Clevers, Hans ;
Stunnenberg, Hendrik G. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (08) :2732-2744
[28]   Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome [J].
Heintzman, Nathaniel D. ;
Stuart, Rhona K. ;
Hon, Gary ;
Fu, Yutao ;
Ching, Christina W. ;
Hawkins, R. David ;
Barrera, Leah O. ;
Van Calcar, Sara ;
Qu, Chunxu ;
Ching, Keith A. ;
Wang, Wei ;
Weng, Zhiping ;
Green, Roland D. ;
Crawford, Gregory E. ;
Ren, Bing .
NATURE GENETICS, 2007, 39 (03) :311-318
[29]   Histone modifications at human enhancers reflect global cell-type-specific gene expression [J].
Heintzman, Nathaniel D. ;
Hon, Gary C. ;
Hawkins, R. David ;
Kheradpour, Pouya ;
Stark, Alexander ;
Harp, Lindsey F. ;
Ye, Zhen ;
Lee, Leonard K. ;
Stuart, Rhona K. ;
Ching, Christina W. ;
Ching, Keith A. ;
Antosiewicz-Bourget, Jessica E. ;
Liu, Hui ;
Zhang, Xinmin ;
Green, Roland D. ;
Lobanenkov, Victor V. ;
Stewart, Ron ;
Thomson, James A. ;
Crawford, Gregory E. ;
Kellis, Manolis ;
Ren, Bing .
NATURE, 2009, 459 (7243) :108-112
[30]   Early chromatin unfolding by RUNX1: a molecular explanation for differential requirements during specification versus maintenance of the hematopoietic gene expression program [J].
Hoogenkamp, Maarten ;
Lichtinger, Monika ;
Krysinska, Hanna ;
Lancrin, Christophe ;
Clarke, Deborah ;
Williamson, Andrew ;
Mazzarella, Luca ;
Ingram, Richard ;
Jorgensen, Helle ;
Fisher, Amanda ;
Tenen, Daniel G. ;
Kouskoff, Valerie ;
Lacaud, Georges ;
Bonifer, Constanze .
BLOOD, 2009, 114 (02) :299-309