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1
The Saccharomyces cerevisiae Msh2 mismatch repair protein localizes to recombination intermediates in vivo.酿酒酵母Msh2错配修复蛋白在体内定位于重组中间体。
Mol Cell. 2000 May;5(5):789-99. doi: 10.1016/s1097-2765(00)80319-6.
2
Evidence for short-patch mismatch repair in Saccharomyces cerevisiae.酿酒酵母中短补丁错配修复的证据。
EMBO J. 2000 Jul 3;19(13):3408-17. doi: 10.1093/emboj/19.13.3408.
3
(CA/GT)(n) microsatellites affect homologous recombination during yeast meiosis.(CA/GT)(n)微卫星在酵母减数分裂过程中影响同源重组。
Genes Dev. 2000 May 15;14(10):1261-8.
4
Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae.酿酒酵母中双链断裂诱导的多种重组途径。
Microbiol Mol Biol Rev. 1999 Jun;63(2):349-404. doi: 10.1128/MMBR.63.2.349-404.1999.
5
The role of the mismatch repair machinery in regulating mitotic and meiotic recombination between diverged sequences in yeast.错配修复机制在调控酵母中分歧序列间有丝分裂和减数分裂重组中的作用。
Genetics. 1999 Apr;151(4):1299-313. doi: 10.1093/genetics/151.4.1299.
6
Eukaryotic DNA mismatch repair.真核生物DNA错配修复
Curr Opin Genet Dev. 1999 Feb;9(1):89-96. doi: 10.1016/s0959-437x(99)80013-6.
7
'Saccharomyces cerevisiae MSH2/6 complex interacts with Holliday junctions and facilitates their cleavage by phage resolution enzymes.酿酒酵母MSH2/6复合物与霍利迪连接体相互作用,并促进噬菌体解离酶对其进行切割。
J Biol Chem. 1999 Mar 12;274(11):7200-6. doi: 10.1074/jbc.274.11.7200.
8
Triplet repeats form secondary structures that escape DNA repair in yeast.三核苷酸重复序列形成的二级结构可逃避酵母中的DNA修复。
Proc Natl Acad Sci U S A. 1999 Feb 16;96(4):1504-9. doi: 10.1073/pnas.96.4.1504.
9
Conserved sequence preference in DNA binding among recombination proteins: an effect of ssDNA secondary structure.重组蛋白中DNA结合的保守序列偏好:单链DNA二级结构的影响
Nucleic Acids Res. 1999 Jan 15;27(2):596-600. doi: 10.1093/nar/27.2.596.
10
Role of MutS ATPase activity in MutS,L-dependent block of in vitro strand transfer.MutS 腺苷三磷酸酶活性在 MutS、L 依赖性体外链转移阻断中的作用
J Biol Chem. 1998 Sep 4;273(36):23176-82. doi: 10.1074/jbc.273.36.23176.

(CA/TG)微卫星序列在酿酒酵母中可逃避错配修复对重组的抑制作用。

(CA/TG) microsatellite sequences escape the inhibition of recombination by mismatch repair in Saccharomyces cerevisiae.

作者信息

Gendrel C G, Dutreix M

机构信息

UMR-CNRS 2027, Institut Curie-section de Recherche, Université Paris-Sud, F-91405 Orsay, France.

出版信息

Genetics. 2001 Dec;159(4):1539-45. doi: 10.1093/genetics/159.4.1539.

DOI:10.1093/genetics/159.4.1539
PMID:11779795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1461888/
Abstract

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.

摘要

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。