Genetic basis for primordial germ cells specification in mouse and human: Conserved and divergent roles of PRDM and SOX transcription factors

被引:24
作者
Sybirna, Anastasiya [1 ,2 ,3 ]
Wong, Frederick C. K. [1 ,2 ]
Surani, M. Azim [1 ,2 ,3 ]
机构
[1] Univ Cambridge, Wellcome Trust Canc Res UK Gurdon Inst, Cambridge, England
[2] Univ Cambridge, Physiol Dev & Neurosci Dept, Cambridge, England
[3] Univ Cambridge, Wellcome Trust Med Res Council Cambridge Stem Cel, Cambridge, England
来源
IMMORTAL GERMLINE | 2019年 / 135卷
基金
英国惠康基金;
关键词
EMBRYONIC STEM-CELLS; DNA DEMETHYLATION DYNAMICS; IN-VITRO; NAIVE PLURIPOTENCY; MARMOSET MONKEY; SYNERGISTIC ACTION; SELF-ORGANIZATION; AXIS FORMATION; TERMINAL DIFFERENTIATION; REGULATES PLURIPOTENCY;
D O I
10.1016/bs.ctdb.2019.04.004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Primordial germ cells (PGCs) are embryonic precursors of sperm and egg that pass on genetic and epigenetic information from one generation to the next. In mammals, they are induced from a subset of cells in peri-implantation epiblast by BMP signaling from the surrounding tissues. PGCs then initiate a unique developmental program that involves comprehensive epigenetic resetting and repression of somatic genes. This is orchestrated by a set of signaling molecules and transcription factors that promote germ cell identity. Here we review significant findings on mammalian PGC biology, in particular, the genetic basis for PGC specification in mice and human, which has revealed an evolutionary divergence between the two species. We discuss the importance and potential basis for these differences and focus on several examples to illustrate the conserved and divergent roles of critical transcription factors in mouse and human germline.
引用
收藏
页码:35 / 89
页数:55
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