Epigenetic landscape required for placental development

被引:86
作者
Hemberger, M. [1 ]
机构
[1] Babraham Inst, Cambridge CB22 3AT, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
extraembryonic tissues; trophoblast; placenta; development; chromatin; epigenetics;
D O I
10.1007/s00018-007-7113-z
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
Formation of extraembryonic tissues, and in particular the placenta, is an absolute necessity to ensure growth and survival of the embryo during intrauterine development in mammals. To date, an intriguing number of genes have been identified that are essential for development of extraembryonic structures. However, the underlying genetic information must be interpreted by a set of epigenetic instructions to both establish and maintain lineage- and cell type-specific expression profiles. Based on accumulating data in particular from studies in the mouse, this article is aimed at highlighting the epigenetic machinery required for differentiation of extraembryonic cell types and formation of the placenta. An overview of knockout models reveals key stages in extraembryonic development that are particularly sensitive to alterations in the chromatin environment. The article also summarizes the importance of complex epigenetically controlled mechanisms for placental development, such as imprinted gene expression and imprinted X chromosome inactivation. These investigations of the epigenetic regulation of transcriptional states will provide valuable insights into the dynamic chromatin environment that is specific to extraembryonic tissues and determines gene expression patterns required for normal trophoblast differentiation.
引用
收藏
页码:2422 / 2436
页数:15
相关论文
共 124 条
[71]  
Okamoto I, 2000, DEVELOPMENT, V127, P4137
[72]   Epigenetic dynamics of imprinted X inactivation during early mouse development [J].
Okamoto, I ;
Otte, AP ;
Allis, CD ;
Reinberg, D ;
Heard, E .
SCIENCE, 2004, 303 (5658) :644-649
[73]   DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development [J].
Okano, M ;
Bell, DW ;
Haber, DA ;
Li, E .
CELL, 1999, 99 (03) :247-257
[74]   Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality [J].
Ono, R ;
Nakamura, K ;
Inoue, K ;
Naruse, M ;
Usami, T ;
Wakisaka-Saito, N ;
Hino, T ;
Suzuki-Migishima, R ;
Ogonuki, N ;
Miki, H ;
Kohda, T ;
Ogura, A ;
Yokoyama, M ;
Kaneko-Ishino, T ;
Ishino, F .
NATURE GENETICS, 2006, 38 (01) :101-106
[75]   Suz12 is essential for mouse development and for EZH2 histone methyltransferase activity [J].
Pasini, D ;
Bracken, AP ;
Jensen, MR ;
Denchi, EL ;
Helin, K .
EMBO JOURNAL, 2004, 23 (20) :4061-4071
[76]   Arginine N-methyltransferase 1 is required for early postimplantation mouse development, but cells deficient in the enzyme are viable [J].
Pawlak, MR ;
Scherer, CA ;
Chen, J ;
Roshon, MJ ;
Ruley, HE .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (13) :4859-4869
[77]   Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability [J].
Peters, AHFM ;
O'Carroll, D ;
Scherthan, H ;
Mechtler, K ;
Sauer, S ;
Schöfer, C ;
Weipoltshammer, K ;
Pagani, M ;
Lachner, M ;
Kohlmaier, A ;
Opravil, S ;
Doyle, M ;
Sibilia, M ;
Jenuwein, T .
CELL, 2001, 107 (03) :323-337
[78]   An update on embryo culture for human assisted reproductive technology: Media, performance, and safety [J].
Pool, TB .
SEMINARS IN REPRODUCTIVE MEDICINE, 2005, 23 (04) :309-318
[79]   Epigenetic regulation of human trophoblastic cell migration and invasion [J].
Rahnama, Fahimeh ;
Shafiei, Farhad ;
Gluckman, Peter D. ;
Mitchell, Murray D. ;
Lobie, Peter E. .
ENDOCRINOLOGY, 2006, 147 (11) :5275-5283
[80]   NSD1 is essential for early post-implantation development and has a catalytically active SET domain [J].
Rayasam, GV ;
Wendling, O ;
Angrand, PO ;
Mark, M ;
Niederreither, K ;
Song, L ;
Lerouge, T ;
Hager, GL ;
Chambon, P ;
Losson, R .
EMBO JOURNAL, 2003, 22 (12) :3153-3163