Importance of base-pair opening for mismatch recognition
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
33080020
PubMed Central
PMC7672436
DOI
10.1093/nar/gkaa896
PII: 5932846
Knihovny.cz E-zdroje
- MeSH
- chybné párování bází * MeSH
- DNA chemie metabolismus MeSH
- oprava chybného párování bází DNA * MeSH
- párování bází MeSH
- simulace molekulární dynamiky * MeSH
- termodynamika MeSH
- vazebný protein MutS opravné syntézy DNA chemie genetika metabolismus MeSH
- vodíková vazba MeSH
- výpočetní biologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA MeSH
- vazebný protein MutS opravné syntézy DNA MeSH
Mismatch repair is a highly conserved cellular pathway responsible for repairing mismatched dsDNA. Errors are detected by the MutS enzyme, which most likely senses altered mechanical property of damaged dsDNA rather than a specific molecular pattern. While the curved shape of dsDNA in crystallographic MutS/DNA structures suggests the role of DNA bending, the theoretical support is not fully convincing. Here, we present a computational study focused on a base-pair opening into the minor groove, a specific base-pair motion observed upon interaction with MutS. Propensities for the opening were evaluated in terms of two base-pair parameters: Opening and Shear. We tested all possible base pairs in anti/anti, anti/syn and syn/anti orientations and found clear discrimination between mismatches and canonical base-pairs only for the opening into the minor groove. Besides, the discrimination gap was also confirmed in hotspot and coldspot sequences, indicating that the opening could play a more significant role in the mismatch recognition than previously recognized. Our findings can be helpful for a better understanding of sequence-dependent mutability. Further, detailed structural characterization of mismatches can serve for designing anti-cancer drugs targeting mismatched base pairs.
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