H3K9/HP1 and Polycomb: Two Key Epigenetic Silencing Pathways for Gene Regulation and Embryo Development

被引:38
作者
Nestorov, Peter [1 ,2 ]
Tardat, Mathieu [1 ]
Peters, Antoine H. F. M. [1 ,2 ]
机构
[1] Friedrich Miescher Inst Biomed Res, Basel, Switzerland
[2] Univ Basel, Fac Sci, Basel, Switzerland
来源
EPIGENETICS AND DEVELOPMENT | 2013年 / 104卷
关键词
NOVO DNA METHYLATION; REPRESSIVE COMPLEX 1; HISTONE H3 LYSINE-9; HETEROCHROMATIN PROTEIN-1 HOMOLOG; JMJC DOMAIN PROTEIN; STEM-CELLS; METHYLTRANSFERASE G9A; MAMMALIAN HETEROCHROMATIN; ENDOGENOUS RETROVIRUSES; CHROMATIN CONDENSATION;
D O I
10.1016/B978-0-12-416027-9.00008-5
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proper development of an embryo requires tightly controlled expression of specific sets of genes. In order to generate all the lineages of the adult, populations of pluripotent embryonic stem cells differentiate and activate specific transcriptional programs whereas others are shutdown. The role of transcription factors is obvious in promoting expression of such developmental genes; however maintenance of specific states throughout cell division needs additional mechanisms. Indeed, the nucleoprotein complex of DNA and histones, the chromatin, can act as a facilitator or barrier to transcription depending on its configuration. Chromatin-modifying enzymes regulate accessibility of DNA by establishing specific sets of chromatin, which will be either permissive or repressive to transcription. In this review, we will describe the H3K9/HP1 and Polycomb pathways, which mediate transcriptional repression by modifying chromatin. We discuss how these two major epigenetic silencing modes are dynamically regulated and how they contribute to the early steps of embryo development.
引用
收藏
页码:243 / 291
页数:49
相关论文
共 302 条
[61]   Histone H2A Mono-Ubiquitination Is a Crucial Step to Mediate PRC1-Dependent Repression of Developmental Genes to Maintain ES Cell Identity [J].
Endoh, Mitsuhiro ;
Endo, Takaho A. ;
Endoh, Tamie ;
Isono, Kyo-ichi ;
Sharif, Jafar ;
Ohara, Osamu ;
Toyoda, Tetsuro ;
Ito, Takashi ;
Eskeland, Ragnhild ;
Bickmore, Wendy A. ;
Vidal, Miguel ;
Bernstein, Bradley E. ;
Koseki, Haruhiko .
PLOS GENETICS, 2012, 8 (07)
[62]   De novo DNA methylation promoted by G9a prevents reprogramming of embryonically silenced genes [J].
Epsztejn-Litman, Silvina ;
Feldman, Nirit ;
Abu-Remaileh, Monther ;
Shufaro, Yoel ;
Gerson, Ariela ;
Ueda, Jun ;
Deplus, Rachel ;
Fuks, Francois ;
Shinkai, Yoichi ;
Cedar, Howard ;
Bergman, Yehudit .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2008, 15 (11) :1176-1183
[63]   Direct interaction between DNMT1 and G9a coordinates DNA and histone methylation during replication [J].
Esteve, Pierre-Olivier ;
Chin, Hang Gyeong ;
Smallwood, Andrea ;
Feehery, George R. ;
Gangisetty, Omkaram ;
Karpf, Adam R. ;
Carey, Michael F. ;
Pradhan, Sriharsa .
GENES & DEVELOPMENT, 2006, 20 (22) :3089-3103
[64]   The secret message of heterochromatin: new insights into the mechanisms and function of centromeric and pericentric repeat sequence transcription [J].
Eymery, Angeline ;
Callanan, Mary ;
Vourc'h, Claire .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2009, 53 (2-3) :259-268
[65]   EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair [J].
Ezhkova, Elena ;
Lien, Wen-Hui ;
Stokes, Nicole ;
Pasolli, H. Amalia ;
Silva, Jose M. ;
Fuchs, Elaine .
GENES & DEVELOPMENT, 2011, 25 (05) :485-498
[66]  
Faust C, 1998, DEVELOPMENT, V125, P4495
[67]   G9a-mediated irreversible epigenetic inactivation of Oct-3/4 during early embryogenesis [J].
Feldman, N ;
Gerson, A ;
Fang, J ;
Li, E ;
Zhang, Y ;
Shinkai, Y ;
Cedar, H ;
Bergman, Y .
NATURE CELL BIOLOGY, 2006, 8 (02) :188-U55
[68]   Systematic Protein Location Mapping Reveals Five Principal Chromatin Types in Drosophila Cells [J].
Filion, Guillaume J. ;
van Bemmel, Joke G. ;
Braunschweig, Ulrich ;
Talhout, Wendy ;
Kind, Jop ;
Ward, Lucas D. ;
Brugman, Wim ;
de Castro, Ines J. ;
Kerkhoven, Ron M. ;
Bussemaker, Harmen J. ;
van Steensel, Bas .
CELL, 2010, 143 (02) :212-224
[69]   Regulation of HP1-chromatin binding by histone H3 methylation and phosphorylation [J].
Fischle, W ;
Tseng, BS ;
Dormann, HL ;
Ueberheide, BM ;
Garcia, BA ;
Shabanowitz, J ;
Hunt, DF ;
Funabiki, H ;
Allis, CD .
NATURE, 2005, 438 (7071) :1116-1122
[70]   Molecular basis for the discrimination of repressive methyl-lysine marks in histone H3 bv Polvcomb and HP1 chromodomains [J].
Fischle, W ;
Wang, YM ;
Jacobs, SA ;
Kim, YC ;
Allis, CD ;
Khorasanizadeh, S .
GENES & DEVELOPMENT, 2003, 17 (15) :1870-1881