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脱氨基5-甲基胞嘧啶的错配修复

Mismatch repair of deaminated 5-methyl-cytosine.

作者信息

Jones M, Wagner R, Radman M

出版信息

J Mol Biol. 1987 Mar 5;194(1):155-9. doi: 10.1016/0022-2836(87)90724-8.

Abstract

Deamination of 5-methyl-cytosine in double-stranded DNA produces a G-T mismatch. Heteroduplexes of bacteriophage lambda DNA containing a G-T mismatch at the site of a G-5-meC base-pair in one of the parental phages were constructed and used to transfect Escherichia coli cells. Genetic analysis of the progeny phages derived from such heteroduplexes suggests that, in E. coli, mismatches resulting from the deamination of 5-methyl-cytosine are repaired by a system requiring the E. coli dcm methylase and some, but not all, of the functions of the E. coli methyl-directed mismatch repair system. The repair appears to act only on the G-T mismatch and acts specifically to restore the cytosine methylation sequence.

摘要

双链DNA中5-甲基胞嘧啶的脱氨基作用会产生G-T错配。构建了一种噬菌体λ DNA异源双链体,在其中一个亲本噬菌体的G-5-甲基胞嘧啶碱基对位点存在G-T错配,并用于转染大肠杆菌细胞。对源自此类异源双链体的子代噬菌体进行的遗传分析表明,在大肠杆菌中,由5-甲基胞嘧啶脱氨基产生的错配可通过一个需要大肠杆菌dcm甲基化酶以及大肠杆菌甲基化导向错配修复系统部分而非全部功能的系统进行修复。这种修复似乎仅作用于G-T错配,且专门用于恢复胞嘧啶甲基化序列。

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