The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression

被引:229
作者
Mueller, Jacob L. [1 ,2 ]
Mahadevaiah, Shantha K. [3 ]
Park, Peter J. [4 ]
Warburton, Peter E. [5 ]
Page, David C. [1 ,2 ]
Turner, James M. A. [3 ]
机构
[1] Whitehead Inst, Howard Hughes Med Inst, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] Natl Inst Med Res, MRC, Div Stem Cell Res & Dev Genet, London NW7 1AA, England
[4] Harvard Partners Ctr Genet & Genom, Childrens Hosp Informat Program, Boston, MA 02115 USA
[5] Mt Sinai Sch Med, Dept Human Genet, New York, NY 10029 USA
基金
英国医学研究理事会;
关键词
D O I
10.1038/ng.126
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
According to the prevailing view, mammalian X chromosomes are enriched in spermatogenesis genes expressed before meiosis(1-3) and deficient in spermatogenesis genes expressed after meiosis(2,3).The paucity of postmeiotic genes on the X chromosome has been interpreted as a consequence of meiotic sex chromosome inactivation (MSCI)-the complete silencing of genes on the XY bivalent at meiotic prophase(4,5). Recent studies have concluded that MSCI-initiated silencing persists beyond meiosis(6-8) and that most genes on the X chromosome remain repressed in round spermatids(7). Here, we report that 33 multicopy gene families, representing similar to 273 mouse X-linked genes, are expressed in the testis and that this expression is predominantly in postmeiotic cells. RNA FISH and microarray analysis show that the maintenance of X chromosome postmeiotic repression is incomplete. Furthermore, X-linked multicopy genes exhibit a similar degree of expression as autosomal genes. Thus, not only is the mouse X chromosome enriched for spermatogenesis genes functioning before meiosis, but in addition, similar to 18% of mouse X-linked genes are expressed in postmeiotic cells.
引用
收藏
页码:794 / 799
页数:6
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