Testicular degeneration in Bclw-deficient mice

被引:214
作者
Ross, AJ
Waymire, KG
Moss, JE
Parlow, AF
Skinner, MK
Russell, LD
MacGregor, GR
机构
[1] Emory Univ, Sch Med, Ctr Mol Med, Atlanta, GA 30322 USA
[2] Univ Edinburgh, BBSRC, Ctr Genome Res, Edinburgh EH9 3JQ, Midlothian, Scotland
[3] Harbor UCLA Med Ctr, Torrance, CA 90509 USA
[4] Washington State Univ, Dept Genet & Cell Biol, Ctr Reprod Biol, Pullman, WA 99164 USA
[5] So Illinois Univ, Sch Med, Dept Physiol, Carbondale, IL 62901 USA
关键词
D O I
10.1038/ng0398-251
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To identify genes required for mammalian spermatogenesis, we screened lines of mutant mice created using a retroviral gene-trap system(1) for male infertility. Homozygous ROSA41 male mice exhibit sterility associated with progressive testicular degeneration. Germ-cell defects are first observed at 19 clays 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.
引用
收藏
页码:251 / 256
页数:6
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