Literature DB >> 25342176

An ENU-induced mutation in the mouse Rnf212 gene is associated with male meiotic failure and infertility.

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.
© 2015 Society for Reproduction and Fertility.

Entities:  

Keywords:  crossing over; meiosis; mouse; repro57; spermatogenesis

Mesh:

Substances:

Year:  2014        PMID: 25342176      PMCID: PMC4248014          DOI: 10.1530/REP-14-0122

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  34 in total

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