Characterization of Enhancer Function from Genome-Wide Analyses

被引:73
作者
Maston, Glenn A. [1 ,2 ,3 ]
Landt, Stephen G. [4 ]
Snyder, Michael [4 ]
Green, Michael R. [1 ,2 ,3 ]
机构
[1] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[3] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[4] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
来源
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 13 | 2012年 / 13卷
关键词
ChIP-Seq; chromatin; pioneer factors; poised enhancers and promoters; transcriptional competence; location analysis; RNA-POLYMERASE-II; CIS-REGULATORY MODULES; TISSUE-SPECIFIC ENHANCERS; FACTOR-BINDING-SITES; TRANSCRIPTION FACTORS; CHIP-SEQ; GENE-EXPRESSION; CHROMATIN SIGNATURES; NUCLEOSOME ORGANIZATION; NONCODING RNAS;
D O I
10.1146/annurev-genom-090711-163723
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There has been a recent surge in the use of genome-wide methodologies to identify and annotate the transcriptional regulatory elements in the human genome. Here we review some of these methodologies and the conceptual insights about transcription regulation that have been gained from the use of genome-wide studies. It has become clear that the binding of transcription factors is itself a highly regulated process, and binding does not always appear to have functional consequences. Numerous properties have now been associated with regulatory elements that may be useful in their identification. Several aspects of enhancer function have been shown to be more widespread than was previously appreciated, including the highly combinatorial nature of transcription factor binding, the postinitiation regulation of many target genes, and the binding of enhancers at early stages to maintain their competence during development. Going forward, the integration of multiple genome-wide data sets should become a standard approach to elucidate higher-order regulatory interactions.
引用
收藏
页码:29 / 57
页数:29
相关论文
共 186 条
[1]   Noncoding transcription controls downstream promoters to regulate T-cell receptor α recombination [J].
Abarrategui, Iratxe ;
Krangel, Michael S. .
EMBO JOURNAL, 2007, 26 (20) :4380-4390
[2]   Mapping accessible chromatin regions using Sono-Seq [J].
Auerbach, Raymond K. ;
Euskirchen, Ghia ;
Rozowsky, Joel ;
Lamarre-Vincent, Nathan ;
Moqtaderi, Zarmik ;
Lefrancois, Philippe ;
Struhl, Kevin ;
Gerstein, Mark ;
Snyder, Michael .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (35) :14926-14931
[3]   A BLOCK TO ELONGATION IS LARGELY RESPONSIBLE FOR DECREASED TRANSCRIPTION OF C-MYC IN DIFFERENTIATED HL60 CELLS [J].
BENTLEY, DL ;
GROUDINE, M .
NATURE, 1986, 321 (6071) :702-706
[4]   Sequentially acting Sox transcription factors in neural lineage development [J].
Bergsland, Maria ;
Ramskold, Daniel ;
Zaouter, Cecile ;
Klum, Susanne ;
Sandberg, Rickard ;
Muhr, Jonas .
GENES & DEVELOPMENT, 2011, 25 (23) :2453-2464
[5]   Transcription Factor AP1 Potentiates Chromatin Accessibility and Glucocorticoid Receptor Binding [J].
Biddie, Simon C. ;
John, Sam ;
Sabo, Pete J. ;
Thurman, Robert E. ;
Johnson, Thomas A. ;
Schiltz, R. Louis ;
Miranda, Tina B. ;
Sung, Myong-Hee ;
Trump, Saskia ;
Lightman, Stafford L. ;
Vinson, Charles ;
Stamatoyannopoulos, John A. ;
Hager, Gordon L. .
MOLECULAR CELL, 2011, 43 (01) :145-155
[6]   Animal Transcription Networks as Highly Connected, Quantitative Continua [J].
Biggin, Mark D. .
DEVELOPMENTAL CELL, 2011, 21 (04) :611-626
[7]   THE ESSENTIALS OF DNA METHYLATION [J].
BIRD, A .
CELL, 1992, 70 (01) :5-8
[8]   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
[9]   Genome-wide computational prediction of transcriptional regulatory modules reveals new insights into human gene expression [J].
Blanchette, M ;
Bataille, AR ;
Chen, XY ;
Poitras, C ;
Laganière, J ;
Lefèbvre, C ;
Deblois, G ;
Giguère, V ;
Ferretti, V ;
Bergeron, D ;
Coulombe, B ;
Robert, FO .
GENOME RESEARCH, 2006, 16 (05) :656-668
[10]   ChIP-Seq identification of weakly conserved heart enhancers [J].
Blow, Matthew J. ;
McCulley, David J. ;
Li, Zirong ;
Zhang, Tao ;
Akiyama, Jennifer A. ;
Holt, Amy ;
Plajzer-Frick, Ingrid ;
Shoukry, Malak ;
Wright, Crystal ;
Chen, Feng ;
Afzal, Veena ;
Bristow, James ;
Ren, Bing ;
Black, Brian L. ;
Rubin, Edward M. ;
Visel, Axel ;
Pennacchio, Len A. .
NATURE GENETICS, 2010, 42 (09) :806-U107