SCML2 establishes the male germline epigenome through regulation of histone H2A ubiquitination.

SCML2 establishes the male germline epigenome through regulation of histone H2A ubiquitination.
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DOI:
10.1016/j.devcel.2015.01.014
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发表时间:
2015-03-09
期刊:
影响因子:
11.8
通讯作者:
Namekawa, Satoshi H.
Namekawa, Satoshi H.
中科院分区:
生物学1区
文献类型:
--
作者:
Hasegawa, Kazuteru;Sin, Ho-Su;Maezawa, So;Broering, Tyler J.;Kartashov, Andrey V.;Alavattam, Kris G.;Ichijima, Yosuke;Zhang, Fan;Bacon, W. Clark;Greis, Kenneth D.;Andreassen, Paul R.;Barski, Artem;Namekawa, Satoshi H.

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Gametogenesis is dependent on the expression of germline-specific genes. However, it remains unknown how the germline epigenome is distinctly established from that of somatic lineages. Here we show that genes commonly expressed in somatic lineages and spermatogenesis-progenitor cells undergo repression in a genome-wide manner in late stages of the male germline and identify underlying mechanisms. SCML2, a germline-specific subunit of a Polycomb repressive complex 1 (PRC1), establishes the unique epigenome of the male germline through two distinct antithetical mechanisms. SCML2 works with PRC1 and promotes RNF2-dependent ubiquitination of H2A, thereby marking somatic/progenitor genes on autosomes for repression. Paradoxically, SCML2 also prevents RNF2-dependent ubiquitination of H2A on sex chromosomes during meiosis, thereby enabling unique epigenetic programming of sex chromosomes for male reproduction. Our results reveal divergent mechanisms involving a shared regulator by which the male germline epigenome is distinguished from that of the soma and progenitor cells.
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