Maintenance of spermatogenesis requires TAF4b, a gonad-specific subunit of TFIID

被引:178
|
作者
Falender, AE
Freiman, RN
Geles, KG
Lo, KC
Hwang, K
Lamb, DJ
Morris, PL
Tjian, R
Richards, JS [1 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Scott Dept Urol, Houston, TX 77030 USA
[3] Brown Univ, Dept Mol & Cell Biol & Biochem, Providence, RI 02921 USA
[4] Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[5] Univ Toronto, Mt Sinai Hosp, Div Urol, Toronto, ON M5G 1X5, Canada
[6] Rockefeller Univ, Populat Council, New York, NY 10021 USA
关键词
spermatogonial stem cell; Taf4b; germ cell; Stra8; c-Ret;
D O I
10.1101/gad.1290105
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The establishment and maintenance of spermatogenesis in mammals requires specialized networks of gene expression programs in the testis. The gonad-specific TAF4b component of TFIID (formerly TAF(Pi)105) is a transcriptional regulator enriched in the mouse testis. Herein we show that TAF4b is required for maintenance of spermatogenesis in the mouse. While young Taf4b-null males are initially fertile, Taf4b-null males become infertile by 3 mo of age and eventually exhibit seminiferous tubules devoid of germ cells. At birth, testes of Taf4b-null males appear histologically normal; however, at post-natal day 3 gonocyte proliferation is impaired and expression of spermatogonial stem cell markers c-Ret, Plzf, and Stra8 is reduced. Together, these data indicate that TAF4b is required for the precise expression of gene products essential for germ cell proliferation and suggest that TAF4b may be required for the regulation of spermatogonial stem cell specification and proliferation that is obligatory for normal spermatogenic maintenance in the adult.
引用
收藏
页码:794 / 803
页数:10
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