The yeast MSH1 gene is not involved in DNA repair or recombination during meiosis

被引:10
作者
Sia, EA
Kirkpatrick, DT
机构
[1] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[2] Univ Rochester, Dept Biol, Rochester, NY 14627 USA
关键词
MSH1; mismatch repair; meiosis; MutS; recombination; mitochondria;
D O I
10.1016/j.dnarep.2004.10.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Six strong homologs of the bacterial MutS DNA mismatch repair (MMR) gene have been identified in the yeast Saccharomyces cerevisiae. With the exception of the MSH1 gene, the involvement of each homolog in DNA repair and recombination during meiosis has been determined previously. Five of the homologs have been demonstrated to act in meiotic DNA repair (MSH2, MSH3, MSH6 and MSH4) and/or meiotic recombination (MSH4 and MSH5). Unfortunately the loss of mitochondrial function that results from deletion of MSH1 disrupts meiotic progression, precluding an analysis of MSH1 function in meiotic DNA repair and recombination. However, the recent identification of two separation-of-function alleles of MSH1 that interfere with protein function but still maintain functional mitochondria allow the meiotic activities of MSH1 to be determined. We show that the G776D and F105A alleles of MSH1 exhibit no defects in meiotic recombination, repair base-base mismatches and large loop mismatches efficiently during meiosis, and have high levels of spore viability. These data indicate that the MSH1 protein, unlike other MutS homologs in yeast, plays no role in DNA repair or recombination during meiosis. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:253 / 261
页数:9
相关论文
共 44 条
[1]  
ALANI E, 1994, GENETICS, V137, P19
[2]   Genetic and biochemical analysis of Msh2p-Msh6p: Role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition [J].
Alani, E ;
Sokolsky, T ;
Studamire, B ;
Miret, JJ ;
Lahue, RS .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (05) :2436-2447
[3]   A POSITIVE SELECTION FOR MUTANTS LACKING OROTIDINE-5'-PHOSPHATE DECARBOXYLASE ACTIVITY IN YEAST - 5-FLUORO-OROTIC ACID RESISTANCE [J].
BOEKE, JD ;
LACROUTE, F ;
FINK, GR .
MOLECULAR & GENERAL GENETICS, 1984, 197 (02) :345-346
[4]   A mutation in the MSH6 subunit of the Saccharomyces cerevisiae MSH2-MSH6 complex disrupts mismatch recognition [J].
Bowers, J ;
Sokolsky, T ;
Quach, T ;
Alani, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (23) :16115-16125
[5]  
CHI NW, 1994, J BIOL CHEM, V269, P29984
[6]   MULTIFUNCTIONAL YEAST HIGH-COPY-NUMBER SHUTTLE VECTORS [J].
CHRISTIANSON, TW ;
SIKORSKI, RS ;
DANTE, M ;
SHERO, JH ;
HIETER, P .
GENE, 1992, 110 (01) :119-122
[7]   REPAIR OF SPECIFIC BASE PAIR MISMATCHES FORMED DURING MEIOTIC RECOMBINATION IN THE YEAST SACCHAROMYCES-CEREVISIAE [J].
DETLOFF, P ;
SIEBER, J ;
PETES, TD .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (02) :737-745
[8]  
DETLOFF P, 1992, GENETICS, V132, P113
[9]   Evidence for sequential action of two ATPase active sites in yeast Msh2-Msh6 [J].
Drotschmann, K ;
Yang, W ;
Kunkel, TA .
DNA REPAIR, 2002, 1 (09) :743-753
[10]   Asymmetric recognition of DNA local distortion - Structure-based functional studies of eukaryotic Msh2-Msh6 [J].
Drotschmann, K ;
Yang, W ;
Brownewell, FE ;
Kool, ET ;
Kunkel, TA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (49) :46225-46229