Molecular Signals of Epigenetic States

被引:666
作者
Bonasio, Roberto
Tu, Shengjiang
Reinberg, Danny [1 ]
机构
[1] NYU, Howard Hughes Med Inst, New York, NY 10016 USA
关键词
H3; LYSINE-9; METHYLATION; NOVO DNA METHYLATION; HISTONE H3; CHROMATIN; POLYCOMB; RNA; TRANSCRIPTION; REQUIRES; MEMORY; CELLS;
D O I
10.1126/science.1191078
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 ; 0710 ; 09 ;
摘要
Epigenetic signals are responsible for the establishment, maintenance, and reversal of metastable transcriptional states that are fundamental for the cell's ability to "remember" past events, such as changes in the external environment or developmental cues. Complex epigenetic states are orchestrated by several converging and reinforcing signals, including transcription factors, noncoding RNAs, DNA methylation, and histone modifications. Although all of these pathways modulate transcription from chromatin in vivo, the mechanisms by which epigenetic information is transmitted through cell division remain unclear. Because epigenetic states are metastable and change in response to the appropriate signals, a deeper understanding of their molecular framework will allow us to tackle the dysregulation of epigenetics in disease.
引用
收藏
页码:612 / 616
页数:5
相关论文
共 81 条
[1]  
Alvarado A.Sanchez., 2006, CELL, V124, P241, DOI DOI 10.1016/J.CELL.2006.01.012
[2]  
[Anonymous], 2006, An introduction to systems biology: design principles of biological circuits, DOI DOI 10.1201/9781420011432
[3]   A piRNA pathway primed by individual transposons is linked to de novo DNA methylation in mice [J].
Aravin, Alexei A. ;
Sachidanandam, Ravi ;
Bourc'his, Deborah ;
Schaefer, Christopher ;
Pezic, Dubravka ;
Toth, Katalin Fejes ;
Bestor, Timothy ;
Hannon, Gregory J. .
MOLECULAR CELL, 2008, 31 (06) :785-799
[4]   Making a commitment: cell lineage allocation and axis patterning in the early mouse embryo [J].
Arnold, Sebastian J. ;
Robertson, Elizabeth J. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (02) :91-103
[5]   Stc1: A Critical Link between RNAi and Chromatin Modification Required for Heterochromatin Integrity [J].
Bayne, Elizabeth H. ;
White, Sharon A. ;
Kagansky, Alexander ;
Bijos, Dominika A. ;
Sanchez-Pulido, Luis ;
Hoe, Kwang-Lae ;
Kim, Dong-Uk ;
Park, Han-Oh ;
Ponting, Chris P. ;
Rappsilber, Juri ;
Allshire, Robin C. .
CELL, 2010, 140 (05) :666-677
[6]   An operational definition of epigenetics [J].
Berger, Shelley L. ;
Kouzarides, Tony ;
Shiekhattar, Ramin ;
Shilatifard, Ali .
GENES & DEVELOPMENT, 2009, 23 (07) :781-783
[7]   Reprogramming towards pluripotency requires AID-dependent DNA demethylation [J].
Bhutani, Nidhi ;
Brady, Jennifer J. ;
Damian, Mara ;
Sacco, Alessandra ;
Corbel, Stephane Y. ;
Blau, Helen M. .
NATURE, 2010, 463 (7284) :1042-U57
[8]   Perceptions of epigenetics [J].
Bird, Adrian .
NATURE, 2007, 447 (7143) :396-398
[9]   The MT domain of the proto-oncoprotein MLL binds to CpG-containing DNA and discriminates against methylation [J].
Birke, M ;
Schreiner, S ;
García-Cuéllar, MP ;
Mahr, K ;
Titgemeyer, F ;
Slany, RK .
NUCLEIC ACIDS RESEARCH, 2002, 30 (04) :958-965
[10]   A Reconfigured Pattern of MLL Occupancy within Mitotic Chromatin Promotes Rapid Transcriptional Reactivation Following Mitotic Exit [J].
Blobel, Gerd A. ;
Kadauke, Stephan ;
Wang, Eric ;
Lau, Alan W. ;
Zuber, Johannes ;
Chou, Margaret M. ;
Vakoc, Christopher R. .
MOLECULAR CELL, 2009, 36 (06) :970-983