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大肠杆菌尿嘧啶-DNA糖基化酶从U.A碱基对和U.G错配中去除尿嘧啶的序列特异性及其与突变热点的相关性。

Sequence specificity for removal of uracil from U.A pairs and U.G mismatches by uracil-DNA glycosylase from Escherichia coli, and correlation with mutational hotspots.

作者信息

Nilsen H, Yazdankhah S P, Eftedal I, Krokan H E

机构信息

UNIGEN Center for Molecular Biology, University of Trondheim, Norway.

出版信息

FEBS Lett. 1995 Apr 3;362(2):205-9. doi: 10.1016/0014-5793(95)00244-4.

Abstract

The rate of removal of uracil from different positions in double-stranded DNA by uracil-DNA glycosylase from Escherichia coli varied more than 15-fold. Consensus sequences for good and poor removal were 5'-(A/T)UA(A/T)-3' and 5'-(G/C)U(T/G/C)-3', respectively. In general, the sequence context surrounding U was more important for the rate of removal than whether U was present in U.A pairs or U.G mispairs. Rates of removal of U from sites of amber mutations in the lacI gene, where mutation frequencies and deamination rates were known, indicated that the observed variation in removal is biologically significant.

摘要

来自大肠杆菌的尿嘧啶-DNA糖基化酶从双链DNA不同位置去除尿嘧啶的速率变化超过15倍。去除效果好和差的共有序列分别为5'-(A/T)UA(A/T)-3'和5'-(G/C)U(T/G/C)-3'。一般来说,尿嘧啶周围的序列环境对去除速率比尿嘧啶是存在于U·A碱基对还是U·G错配中更为重要。从已知突变频率和脱氨基速率的lacI基因琥珀突变位点去除尿嘧啶的速率表明,观察到的去除差异具有生物学意义。

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