Global patterns of histone modifications

被引:79
作者
Rando, Oliver J. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, Worcester, MA 01605 USA
关键词
D O I
10.1016/j.gde.2007.02.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Histories, the proteins that package eukaryotic genomes into chromatin, are subject to a huge number and variety of covalent modifications. In the past few years, genomic technologies such as microarray hybridization have been applied to the study of histone modifications. These studies shed significant light on the role of covalent modifications in DNA-templated processes. Different histone modifications exhibit distinctive patterns over underlying genomic elements, and these localization patterns reflect the regulatory functions of the relevant modifications. For example, recent results indicate that the localization of H3K36me3 over coding regions reflects its role in shutting down internal transcriptional initiation sites. Histone modifications occur in domains of varying sizes, and the locations of the broadest domains of modifications suggest that broader domains are more likely to be heritable than are shorter modification domains. Importantly, genomic studies reveal that histone modifications tend to co-occur in groups, suggesting that the purpose of histone modifications is not to generate an intricate, complex code, and once again raising the question of why so many histone modifications exist in the cell.
引用
收藏
页码:94 / 99
页数:6
相关论文
共 44 条
[1]   Split decision: What happens to nucleosomes during DNA replication? [J].
Annunziato, AT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (13) :12065-12068
[2]   A bivalent chromatin structure marks key developmental genes in embryonic stem cells [J].
Bernstein, BE ;
Mikkelsen, TS ;
Xie, XH ;
Kamal, M ;
Huebert, DJ ;
Cuff, J ;
Fry, B ;
Meissner, A ;
Wernig, M ;
Plath, K ;
Jaenisch, R ;
Wagschal, A ;
Feil, R ;
Schreiber, SL ;
Lander, ES .
CELL, 2006, 125 (02) :315-326
[3]   Genomic maps and comparative analysis of histone modifications in human and mouse [J].
Bernstein, BE ;
Kamal, M ;
Lindblad-Toh, K ;
Bekiranov, S ;
Bailey, DK ;
Huebert, DJ ;
McMahon, S ;
Karlsson, EK ;
Kulbokas, EJ ;
Gingeras, TR ;
Schreiber, SL ;
Lander, ES .
CELL, 2005, 120 (02) :169-181
[4]   Polycomb complexes repress developmental regulators in murine embryonic stem cells [J].
Boyer, LA ;
Plath, K ;
Zeitlinger, J ;
Brambrink, T ;
Medeiros, LA ;
Lee, TI ;
Levine, SS ;
Wernig, M ;
Tajonar, A ;
Ray, MK ;
Bell, GW ;
Otte, AP ;
Vidal, M ;
Gifford, DK ;
Young, RA ;
Jaenisch, R .
NATURE, 2006, 441 (7091) :349-353
[5]   Histone H3 methylation by Set2 directs deacetylation of coding regions by Rpd3S to suppress spurious intragenic transcription [J].
Carrozza, MJ ;
Li, B ;
Florens, L ;
Suganuma, T ;
Swanson, SK ;
Lee, KK ;
Shia, WJ ;
Anderson, S ;
Yates, J ;
Washburn, MP ;
Workman, JL .
CELL, 2005, 123 (04) :581-592
[6]   Genomic characterization reveals a simple histone H4 acetylation code [J].
Dion, MF ;
Altschuler, SJ ;
Wu, LF ;
Rando, OJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (15) :5501-5506
[7]   The ENCODE (ENCyclopedia of DNA elements) Project [J].
Feingold, EA ;
Good, PJ ;
Guyer, MS ;
Kamholz, S ;
Liefer, L ;
Wetterstrand, K ;
Collins, FS ;
Gingeras, TR ;
Kampa, D ;
Sekinger, EA ;
Cheng, J ;
Hirsch, H ;
Ghosh, S ;
Zhu, Z ;
Pate, S ;
Piccolboni, A ;
Yang, A ;
Tammana, H ;
Bekiranov, S ;
Kapranov, P ;
Harrison, R ;
Church, G ;
Struhl, K ;
Ren, B ;
Kim, TH ;
Barrera, LO ;
Qu, C ;
Van Calcar, S ;
Luna, R ;
Glass, CK ;
Rosenfeld, MG ;
Guigo, R ;
Antonarakis, SE ;
Birney, E ;
Brent, M ;
Pachter, L ;
Reymond, A ;
Dermitzakis, ET ;
Dewey, C ;
Keefe, D ;
Denoeud, F ;
Lagarde, J ;
Ashurst, J ;
Hubbard, T ;
Wesselink, JJ ;
Castelo, R ;
Eyras, E ;
Myers, RM ;
Sidow, A ;
Batzoglou, S .
SCIENCE, 2004, 306 (5696) :636-640
[8]   Controlling the double helix [J].
Felsenfeld, G ;
Groudine, M .
NATURE, 2003, 421 (6921) :448-453
[9]   Mechanisms of transcriptional memory [J].
Francis, NJ ;
Kingston, RE .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2001, 2 (06) :409-421
[10]   Eaf3 chromodomain interaction with methylated H3-K36 links histone deacetylation to Pol II elongation [J].
Joshi, AA ;
Struhl, K .
MOLECULAR CELL, 2005, 20 (06) :971-978