Reprogramming and the mammalian germline: the Weismann barrier revisited

被引:37
|
作者
Sabour, Davood [1 ]
Schoeler, Hans R. [1 ,2 ]
机构
[1] Max Planck Inst Mol Biomed, Dept Cell & Dev Biol, D-48149 Munster, Germany
[2] Univ Munster, Fac Med, D-48149 Munster, Germany
关键词
PLURIPOTENT STEM-CELLS; IN-VITRO; OVARIAN STRUCTURES; MOUSE; GENERATION; DIFFERENTIATION; DERIVATION; SPECIFICATION; FIBROBLASTS; INDUCTION;
D O I
10.1016/j.ceb.2012.08.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The germline represents a unique cell type that can transmit genetic material to the next generation. During early embryonic development, somatic cells give rise to a small population of cells known as germ cells, which eventually differentiate into mature gametes. Germ cells undergo a process of removing and resetting relevant epigenetic information, mainly by DNA demethylation. This extensive epigenetic reprogramming leads to the conversion of germ cells into immortal cells that can pass on the genome to the next generation. In the absence of germline-specific reprogramming, germ cells would preserve the old, parental epigenetic memory, which would prevent the transfer of heritable information to the offspring. On the contrary, somatic cells cannot reset epigenetic information by preserving the full methylation pattern on imprinting genes. In this review, we focus on the capacity of germ cells and somatic cells (soma) to transfer genetic information to the next generation, and thus revisit the Weismann theory of heredity.
引用
收藏
页码:716 / 723
页数:8
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