Baker S M, Plug A W, Prolla T A, Bronner C E, Harris A C, Yao X, Christie D M, Monell C, Arnheim N, Bradley A, Ashley T, Liskay R M
Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland 97201-3098, USA.
Nat Genet. 1996 Jul;13(3):336-42. doi: 10.1038/ng0796-336.
Mice that are deficient in either the Pms2 or Msh2 DNA mismatch repair genes have microsatellite instability and a predisposition to tumours. Interestingly, Pms2-deficient males display sterility associated with abnormal chromosome pairing in meiosis. Here mice deficient in another mismatch repair gene, Mlh1, possess not only microsatellite instability but are also infertile (both males and females). Mlh1-deficient spermatocytes exhibit high levels of prematurely separated chromosomes and arrest in first division meiosis. We also show that Mlh1 appears to localize to sites of crossing over on meiotic chromosomes. Together these findings suggest that Mlh1 is involved in DNA mismatch repair and meiotic crossing over.
缺乏Pms2或Msh2 DNA错配修复基因的小鼠具有微卫星不稳定性且易患肿瘤。有趣的是,缺乏Pms2的雄性小鼠表现出与减数分裂中异常染色体配对相关的不育。在此,缺乏另一种错配修复基因Mlh1的小鼠不仅具有微卫星不稳定性,而且不育(雄性和雌性均如此)。缺乏Mlh1的精母细胞表现出高水平的过早分离染色体并停滞在减数第一次分裂。我们还表明,Mlh1似乎定位于减数分裂染色体上的交叉位点。这些发现共同表明,Mlh1参与DNA错配修复和减数分裂交叉。