Understanding how mismatch repair proteins participate in the repair/anti-recombination decision

被引:59
作者
Chakraborty, Ujani [1 ]
Alani, Eric [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, 459 Biotechnol Bldg, Ithaca, NY 14853 USA
关键词
heteroduplex rejection; DNA mismatch repair; Msh2; Msh6; Msh3; chromatin marks; CELL NUCLEAR ANTIGEN; DNA END-RESECTION; SACCHAROMYCES-CEREVISIAE MSH2; HOMEOLOGOUS RECOMBINATION; HETERODUPLEX REJECTION; MITOTIC RECOMBINATION; MUTL-ALPHA; CHROMOSOMAL REARRANGEMENTS; MEIOTIC RECOMBINATION; REPEAT INSTABILITY;
D O I
10.1093/femsyr/fow071
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mismatch repair (MMR) systems correct DNA mismatches that result from DNA polymerase misincorporation errors. Mismatches also appear in heteroduplex DNA intermediates formed during recombination between nearly identical sequences, and can be corrected by MMR or removed through an unwinding mechanism, known as anti-recombination or heteroduplex rejection. We review studies, primarily in baker's yeast, which support how specific factors can regulate the MMR/anti-recombination decision. Based on recent advances, we present models for how DNA structure, relative amounts of key repair proteins, the timely localization of repair proteins to DNA substrates and epigenetic marks can modulate this critical decision.The authors review studies, primarily in baker's yeast, which support how specific factors can regulate the MMR/anti-recombination decision.The authors review studies, primarily in baker's yeast, which support how specific factors can regulate the MMR/anti-recombination decision.
引用
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页数:12
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共 114 条
[1]   The coordinated functions of the E-coli MutS and MutL proteins in mismatch repair [J].
Acharya, S ;
Foster, PL ;
Brooks, P ;
Fishel, R .
MOLECULAR CELL, 2003, 12 (01) :233-246
[2]   GENOME REARRANGEMENT IN TOP3 MUTANTS OF SACCHAROMYCES-CEREVISIAE REQUIRES A FUNCTIONAL RAD1 EXCISION REPAIR GENE [J].
BAILIS, AM ;
ARTHUR, L ;
ROTHSTEIN, R .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (11) :4988-4993
[3]   DNA Mismatch Repair Interacts with CAF-1-and ASF1A-H3-H4-dependent Histone (H3-H4)2 Tetramer Deposition [J].
Blanko, Elena Rodriges ;
Kadyrova, Lyudmila Y. ;
Kadyrov, Farid A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (17) :9203-9217
[4]   HDAC6-p97/VCP controlled polyubiquitin chain turnover [J].
Boyault, Cyril ;
Gilquin, Benoit ;
Zhang, Yu ;
Rybin, Vladimir ;
Garman, Elspeth ;
Meyer-Klaucke, Wolfram ;
Matthias, Patrick ;
Muller, Christoph W. ;
Khochbin, Saadi .
EMBO JOURNAL, 2006, 25 (14) :3357-3366
[5]   The Mismatch-Binding Factor MutSβ Can Mediate ATR Activation in Response to DNA Double-Strand Breaks [J].
Burdova, Kamila ;
Mihaljevic, Boris ;
Sturzenegger, Andreas ;
Chappidi, Nagaraja ;
Janscak, Pavel .
MOLECULAR CELL, 2015, 59 (04) :603-614
[6]   Sae2 promotes dsDNA endonuclease activity within Mre11-Rad50-Xrs2 to resect DNA breaks [J].
Cannavo, Elda ;
Cejka, Petr .
NATURE, 2014, 514 (7520) :122-+
[7]   DNA end resection by Dna2-Sgs1-RPA and its stimulation by Top3-Rmi1 and Mre11-Rad50-Xrs2 [J].
Cejka, Petr ;
Cannavo, Elda ;
Polaczek, Piotr ;
Masuda-Sasa, Taro ;
Pokharel, Subhash ;
Campbell, Judith L. ;
Kowalczykowski, Stephen C. .
NATURE, 2010, 467 (7311) :112-U149
[8]   The full-length Saccharomyces cerevisiae Sgs1 protein is a vigorous DNA helicase that preferentially unwinds holliday junctions [J].
Cejka P. ;
Kowalczykowski S.C. .
Journal of Biological Chemistry, 2010, 285 (11) :8290-8301
[9]   A Delicate Balance Between Repair and Replication Factors Regulates Recombination Between Divergent DNA Sequences in Saccharomyces cerevisiae [J].
Chakraborty, Ujani ;
George, Carolyn M. ;
Lyndaker, Amy M. ;
Alani, Eric .
GENETICS, 2016, 202 (02) :525-540
[10]   RPA Coordinates DNA End Resection and Prevents Formation of DNA Hairpins [J].
Chen, Huan ;
Lisby, Michael ;
Symington, Lorraine S. .
MOLECULAR CELL, 2013, 50 (04) :589-600