Gendrel C G, Dutreix M
UMR-CNRS 2027, Institut Curie-section de Recherche, Université Paris-Sud, F-91405 Orsay, France.
Genetics. 2001 Dec;159(4):1539-45. doi: 10.1093/genetics/159.4.1539.
Sequence divergence reduces the frequency of recombination, a process that is dependent on the activity of the mismatch repair system. In the yeast Saccharomyces cerevisiae, repair of mismatches results in gene conversion or restoration, whereas failure to repair mismatches results in postmeiotic segregation (PMS). By examining the conversion and PMS in yeast strains deficient in various MMR genes and heterozygous for large inserts (107 bp) with either a mixed sequence or a 39 (CA/TG) repetitive microsatellite sequence, we demonstrate that: (1) the inhibition of conversion by large inserts depends upon a complex containing both Msh2 and Pms1 proteins; (2) conversion is not inhibited if the single-stranded DNA loop in the heteroduplex is the microsatellite sequence; and (3) large heteroduplex loops with random sequence or repetitive sequence might be repaired by two complexes, containing either Msh2 or Pms1. Our results suggest that inhibition of recombination by heterologous inserts and large loop repair are not processed by the same MMR complexes. We propose that the inhibition of conversion by large inserts is due to recognition by the Msh2/Pms1 complex of mismatches created by intrastrand interactions in the heteroduplex loop.
序列差异会降低重组频率,重组过程依赖错配修复系统的活性。在酿酒酵母中,错配修复会导致基因转换或恢复,而错配未能修复则会导致减数分裂后分离(PMS)。通过检测各种错配修复(MMR)基因缺陷且携带混合序列或39(CA/TG)重复微卫星序列的大插入片段(107 bp)的酵母菌株中的基因转换和减数分裂后分离,我们证明:(1)大插入片段对基因转换的抑制取决于同时包含Msh2和Pms1蛋白的复合物;(2)如果异源双链中的单链DNA环是微卫星序列,则基因转换不会受到抑制;(3)具有随机序列或重复序列的大异源双链环可能由包含Msh2或Pms1的两种复合物修复。我们的结果表明,异源插入片段对重组的抑制和大环修复并非由相同的错配修复复合物进行。我们提出,大插入片段对基因转换的抑制是由于Msh2/Pms1复合物识别了异源双链环中链内相互作用产生的错配。