Conformational trapping of Mismatch Recognition Complex MSH2/MSH3 on repair-resistant DNA loops

被引:53
|
作者
Lang, Walter H. [2 ]
Coats, Julie E. [4 ]
Majka, Jerzy [2 ]
Hura, Greg L. [2 ]
Lin, Yuyen [4 ]
Rasnik, Ivan [4 ]
McMurray, Cynthia T. [1 ,2 ,3 ]
机构
[1] Mayo Fdn, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
[3] Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[4] Emory Univ, Dept Phys, Atlanta, GA 30322 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
DNA repair; mismatch repair; smFRET; trinucelotide expansion; SACCHAROMYCES-CEREVISIAE; PROTEIN MUTS; BULGED BASES; REPEAT INSTABILITY; CRYSTAL-STRUCTURE; ATPASE ACTIVITY; BINDING; MOLECULE; MECHANISMS; SCATTERING;
D O I
10.1073/pnas.1105461108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Insertion and deletion of small heteroduplex loops are common mutations in DNA, but why some loops are prone to mutation and others are efficiently repaired is unknown. Here we report that the mismatch recognition complex, MSH2/MSH3, discriminates between a repair-competent and a repair-resistant loop by sensing the conformational dynamics of their junctions. MSH2/MSH3 binds, bends, and dissociates from repair-competent loops to signal downstream repair. Repair-resistant Cytosine-Adenine-Guanine (CAG) loops adopt a unique DNA junction that traps nucleotide-bound MSH2/MSH3, and inhibits its dissociation from the DNA. We envision that junction dynamics is an active participant and a conformational regulator of repair signaling, and governs whether a loop is removed by MSH2/MSH3 or escapes to become a precursor for mutation.
引用
收藏
页码:E837 / E844
页数:8
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