Recognition of GT mismatches by Vsr mismatch endonuclease

被引:18
作者
Fox, KR
Allinson, SL
Sahagun-Krause, H
Brown, T
机构
[1] Univ Southampton, Sch Biol Sci, Dept Biochem & Mol Biol, Southampton SO16 7PX, Hants, England
[2] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
关键词
D O I
10.1093/nar/28.13.2535
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Vsr mismatch endonuclease recognises the sequence CIWGG (W = A or T) in which the underlined thymine is paired with guanine and nicks the DNA backbone on the 5'-side of the mispaired thymine, By using base analogues of G and T we have explored the functional groups on the mismatch pair which are recognised by the enzyme. Removal of the thymine 5-methyl group causes a 60% reduction in activity, while removing the 2-amino group of guanine reduces cleavage by 90%, Placing 2-aminopurine or nebularine opposite T generates mismatches which are cut at a much lower rate (0.1%), When either base is removed, generating a pseudoabasic site (1',2'-dideoxyribose), the enzyme still produces site-specific cleavage, but at only 1% of the original rate. Although TT and CT mismatches at this position are cleaved at a low rate (similar to 1%), mismatches with other bases (such as GA and AC) and Watson-Crick base pairs are not cleaved by the enzyme. There is also no cleavage when the mismatched T is replaced with difluorotoluene.
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页码:2535 / 2540
页数:6
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