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Recognition of GT mismatches by Vsr mismatch endonuclease.

机译:Vsr错配核酸内切酶识别GT错配。

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摘要

The Vsr mismatch endonuclease recognises the sequence CTWGG (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-amino-purine or nebularine opposite T generates mis-matches 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 (approximately 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.
机译:Vsr错配核酸内切酶识别序列CTWGG(W = A或T),其中下划线的胸腺嘧啶与鸟嘌呤配对,并在错配的胸腺嘧啶的5'侧切口DNA主链。通过使用G和T的碱基类似物,我们探索了错配对上被酶识别的官能团。除去胸腺嘧啶5-甲基导致活性降低60%,而除去鸟嘌呤的2-氨基使裂解降低90%。与T相对置的是2个氨基嘌呤或Nebularine,会产生错配,且错配率要低得多(0.1%)。当除去任何一个碱基而产生假核碱基位点(1',2'-二脱氧核糖)时,该酶仍会产生位点特异性裂解,但仅为原始速率的1%。尽管该位置的TT和CT错配率低(大约1%),但与其他碱基(如GA和AC)和Watson-Crick碱基对的错配不会被酶切开。当错配的T被二氟甲苯代替时,也没有裂解。

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