Nuclear Reprogramming in Mouse Primordial Germ Cells: Epigenetic Contribution

被引:21
作者
De Felici, Massimo [1 ]
机构
[1] Univ Roma Tor Vergata, Sect Histol & Embryol, Dept Publ Hlth & Cell Biol, I-00173 Rome, Italy
关键词
EMBRYONIC STEM-CELLS; DE-NOVO METHYLATION; DNA METHYLATION; GENE-EXPRESSION; DEVELOPMENTAL REGULATORS; IN-VITRO; PLURIPOTENT; POLYCOMB; CHROMATIN; GENOME;
D O I
10.4061/2011/425863
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The unique capability of germ cells to give rise to a new organism, allowing the transmission of primary genetic information from generation to generation, depends on their epigenetic reprogramming ability and underlying genomic totipotency. Recent studies have shown that genome-wide epigenetic modifications, referred to as "epigenetic reprogramming", occur during the development of the gamete precursors termed primordial germ cells (PGCs) in the embryo. This reprogramming is likely to be critical for the germ line development itself and necessary to erase the parental imprinting and setting the base for totipotency intrinsic to this cell lineage. The status of genome acquired during reprogramming and the associated expression of key pluripotency genes render PGCs susceptible to transform into pluripotent stem cells. This may occur in vivo under still undefined condition, and it is likely at the origin of the formation of germ cell tumors. The phenomenon appears to be reproduced under partly defined in vitro culture conditions, when PGCs are transformed into embryonic germ (EG) cells. In the present paper, I will try to summarize the contribution that epigenetic modifications give to nuclear reprogramming in mouse PGCs.
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页数:15
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共 120 条
[91]   Tsix silences Xist through modification of chromatin structure [J].
Sado, T ;
Hoki, Y ;
Sasaki, H .
DEVELOPMENTAL CELL, 2005, 9 (01) :159-165
[92]   Mouse germ cell development during embryogenesis [J].
Saga, Yumiko .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2008, 18 (04) :337-341
[93]   A molecular programme for the specification of germ cell fate in mice [J].
Saitou, M ;
Barton, SC ;
Surani, MA .
NATURE, 2002, 418 (6895) :293-300
[94]  
Saraiva Naiara Z, 2010, World J Stem Cells, V2, P121, DOI 10.4252/wjsc.v2.i6.121
[95]   The orphan nuclear receptor GCNF recruits DNA methyltransferase for Oct-314 silencing [J].
Sato, N ;
Kondo, M ;
Arai, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 344 (03) :845-851
[96]   Genome regulation by polycomb and trithorax proteins [J].
Schuettengruber, Bernd ;
Chourrout, Daniel ;
Vervoort, Michel ;
Leblanc, Benjamin ;
Cavalli, Giacomo .
CELL, 2007, 128 (04) :735-745
[97]   Generation of functional multipotent adult stem cells from GPR125+ germline progenitors [J].
Seandel, Marco ;
James, Daylon ;
Shmelkov, Sergey V. ;
Falciatori, Ilaria ;
Kim, Jiyeon ;
Chavala, Sai ;
Scherr, Douglas S. ;
Zhang, Fan ;
Torres, Richard ;
Gale, Nicholas W. ;
Yancopoulos, George D. ;
Murphy, Andrew ;
Valenzuela, David M. ;
Hobbs, Robin M. ;
Pandolfi, Pier Paolo ;
Rafii, Shahin .
NATURE, 2007, 449 (7160) :346-+
[98]   Extensive and orderly reprogramming of genome-wide chromatin modifications associated with specification and early development of germ cells in mice [J].
Seki, Y ;
Hayashi, K ;
Itoh, K ;
Mizugaki, M ;
Saitou, M ;
Matsui, Y .
DEVELOPMENTAL BIOLOGY, 2005, 278 (02) :440-458
[99]   Cellular dynamics associated with the genome-wide epigenetic reprogramming in migrating primordial germ cells in mice [J].
Seki, Yoshiyuki ;
Yamaji, Masashi ;
Yabuta, Yukihiro ;
Sano, Mitsue ;
Shigeta, Mayo ;
Matsui, Yasuhisa ;
Saga, Yumiko ;
Tachibana, Makoto ;
Shinkai, Yoichi ;
Saitou, Mitinori .
DEVELOPMENT, 2007, 134 (14) :2627-2638
[100]   Epigenetic marks by DNA methylation specific to stem, germ and somatic cells in mice [J].
Shiota, K ;
Kogo, Y ;
Ohgane, J ;
Imamura, T ;
Urano, A ;
Nishino, K ;
Tanaka, S ;
Hattori, N .
GENES TO CELLS, 2002, 7 (09) :961-969