Ross A J, Waymire K G, Moss J E, Parlow A F, Skinner M K, Russell L D, MacGregor G R
Center for Molecular Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Nat Genet. 1998 Mar;18(3):251-6. doi: 10.1038/ng0398-251.
To identify genes required for mammalian spermatogenesis, we screened lines of mutant mice created using a retroviral gene-trap system for male infertility. Homozygous ROSA41 male mice exhibit sterility associated with progressive testicular degeneration. Germ-cell defects are first observed at 19 days post-natal (p19). Spermatogenesis is blocked during late spermiogenesis in young adults. Gradual depletion of all stages of germ cells results in a Sertoli-cell-only phenotype by approximately six months of age. Subsequently, almost all Sertoli cells are lost from the seminiferous tubules and the Leydig cell population is reduced. Molecular analysis indicates that the gene mutated is Bclw, a death-protecting member of the Bcl2 family. The mutant allele of Bclw in ROSA41 does not produce a Bclw polypeptide. Expression of Bclw in the testis appears to be restricted to elongating spermatids and Sertoli cells. Potential roles for Bclw in testicular function are discussed.
为了鉴定哺乳动物精子发生所需的基因,我们筛选了利用逆转录病毒基因捕获系统创建的突变小鼠品系,以寻找雄性不育个体。纯合的ROSA41雄性小鼠表现出与进行性睾丸退化相关的不育。生殖细胞缺陷最早在出生后19天(p19)被观察到。在年轻成年小鼠中,精子发生在精子形成后期被阻断。各阶段生殖细胞逐渐耗竭,到大约6月龄时导致仅支持细胞的表型。随后,几乎所有支持细胞从生精小管中消失,间质细胞数量减少。分子分析表明,发生突变的基因是Bclw,它是Bcl2家族中一个具有抗凋亡作用的成员。ROSA41中Bclw的突变等位基因不产生Bclw多肽。Bclw在睾丸中的表达似乎仅限于延长型精子细胞和支持细胞。文中讨论了Bclw在睾丸功能中的潜在作用。