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GATC序列对体外大肠杆菌DNA错配修复的影响。

Influence of GATC sequences on Escherichia coli DNA mismatch repair in vitro.

作者信息

Lu A L

出版信息

J Bacteriol. 1987 Mar;169(3):1254-9. doi: 10.1128/jb.169.3.1254-1259.1987.

Abstract

The effect of the number and position of DNA adenine methylation (dam) sites, i.e., d(GATC) sequences, on mismatch repair in Escherichia coli was investigated. The efficiency of repair was measured in an in vitro assay which used an f1 heteroduplex containing a G/T mismatch within the single EcoRI site. Both an increase in the number of dam sites and a shortened distance between dam site and mismatched site increased the efficiency of mismatch repair. The sequences adjacent to d(GATC) also affected the efficiency of methylation-directed mismatch repair. Furthermore, heteroduplexes with one extra dam site located close to either the 5' or 3' end of the excised base increased the repair efficiency to about the same extent. The findings suggest that the mismatch repair pathway has no preferred polarity.

摘要

研究了DNA腺嘌呤甲基化(dam)位点即d(GATC)序列的数量和位置对大肠杆菌错配修复的影响。在体外试验中测定修复效率,该试验使用了在单个EcoRI位点内含有G/T错配的f1异源双链体。dam位点数量的增加以及dam位点与错配位点之间距离的缩短均提高了错配修复效率。与d(GATC)相邻的序列也影响甲基化导向的错配修复效率。此外,在切除碱基的5'或3'端附近有一个额外dam位点的异源双链体,其修复效率提高到大致相同的程度。这些发现表明错配修复途径没有偏好的极性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8502/211927/6f81d288a76e/jbacter00193-0340-a.jpg

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