| Literature DB >> 25342176 |
Yasuhiro Fujiwara1, Hirokazu Matsumoto2, Kouyou Akiyama2, Anuj Srivastava2, Mizuho Chikushi2, Mary Ann Handel2, Tetsuo Kunieda3.
Abstract
The ENU-induced repro57 mutation was identified in an unbiased screen for the discovery of novel genes for fertility. Male repro57 homozygous mice are infertile and exhibit significantly reduced testis weight compared with WT mice. Histological examination of mutant testes revealed that spermatocytes degenerated during late prophase, and no mature spermatozoa were found in the seminiferous epithelium, suggesting that infertility is caused by the arrest of spermatogenesis at late meiotic prophase. Consistent with this hypothesis, the number of foci with MLH1, a protein essential for crossing over, is greatly reduced in repro57 mutant spermatocytes, which also lack chiasmata between homologs and exhibit premature dissociation of XY chromosomes. In repro57 mutant mice, we identified a mutation in the Rnf212 gene, encoding Ring finger protein 212. The overall phenotype of repro57 mice is consistent with the recently reported phenotype of the Rnf212 knockout mice; slight differences may be due to genetic background effects. Thus, the repro57 nonsense mutation provides a new allele of the mouse Rnf212 gene.Entities:
Keywords: crossing over; meiosis; mouse; repro57; spermatogenesis
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Year: 2014 PMID: 25342176 PMCID: PMC4248014 DOI: 10.1530/REP-14-0122
Source DB: PubMed Journal: Reproduction ISSN: 1470-1626 Impact factor: 3.906