Falender Allison E, Freiman Richard N, Geles Kenneth G, Lo Kirk C, Hwang KeumSil, Lamb Dolores J, Morris Patricia L, Tjian Robert, Richards JoAnne S
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Genes Dev. 2005 Apr 1;19(7):794-803. doi: 10.1101/gad.1290105. Epub 2005 Mar 17.
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(II)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.
哺乳动物精子发生的建立和维持需要睾丸中特定的基因表达程序网络。TFIID的性腺特异性TAF4b成分(以前称为TAF(II)105)是一种在小鼠睾丸中富集的转录调节因子。在此我们表明,TAF4b是小鼠精子发生维持所必需的。虽然年轻的Taf4b基因敲除雄性最初是可育的,但Taf4b基因敲除雄性在3月龄时变得不育,最终表现出没有生殖细胞的生精小管。出生时,Taf4b基因敲除雄性的睾丸在组织学上看起来正常;然而,在出生后第3天,生殖母细胞增殖受损,精原干细胞标志物c-Ret、Plzf和Stra8的表达降低。总之,这些数据表明TAF4b是生殖细胞增殖所必需的基因产物精确表达所必需的,并表明TAF4b可能是调节精原干细胞特化和增殖所必需的,而这对于成年期正常精子发生维持是必不可少的。