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人细胞提取物对DNA中腺嘌呤:胸腺嘧啶碱基对而非鸟嘌呤:O4-甲基胸腺嘧啶碱基对的切割作用。

Incision at diaminopurine: thymine base pairs but not at guanine:O4-methylthymine base pairs in DNA by extracts of human cells.

作者信息

Xu Y Z, Day R S

机构信息

Department of Medicine, Cross Cancer Institute, Edmonton, Alberta, Canada.

出版信息

Biochemistry. 1995 Jun 6;34(22):7438-42. doi: 10.1021/bi00022a017.

Abstract

Cell-free extract from the A1235 human malignant glioma cell line was employed to study the possibility of incision at 2,6-diaminopurine:T (DiAP:T), 2-amino-6-methylaminopurine:T (AMAP:T), and G:O4-methylthymine (G:m4T) mismatches, each placed in a 45 bp DNA at a defined site. The incision of a 45 bp DNA containing a G:T mispair at the same site was followed to determine the relationship between base pair structure and repair activity (ies) in the extract. The cell-free extract incised DNAs containing DiAP:T, AMAP:T, and G:T pairs similarly. Reminiscent of the known pattern of incision at G:T mismatches, products from each substrate were consistent with two incisions, one immediately 5' and one immediately 3' to the mismatched T, and only in the strand containing the mismatched T. While DNA with an O6-methylguanine:T (m6G:T) pair was also incised, DNA containing the G:m4T pair was not, but was rendered inciseable by pretreatment with O6-methylguanine-DNA methyltransferase. Incision of DiAP:T-containing DNA by the extract was less in the presence of unlabeled DNA containing G:T mispairs than in the presence of A:T- or G:A-containing DNA or in the absence of competing DNA. We suggest that the mechanism operating on DiAP:T and/or AMAP:T pairs may be the same as the human G:T repair pathway, possibly initiated by the action of a glycosylase as described by Wiebauer and Jiricny [Wiebauer, K., & Jiricny, J. (1989) Nature 339, 234-236; Wiebauer, K., & Jiricny, J. (1990) Proc. Natl. Acad. Sci, U.S.A. 87, 5842-5845].(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用人恶性胶质瘤细胞系A1235的无细胞提取物,研究了2,6 - 二氨基嘌呤:胸腺嘧啶(DiAP:T)、2 - 氨基 - 6 - 甲基氨基嘌呤:胸腺嘧啶(AMAP:T)和鸟嘌呤:O4 - 甲基胸腺嘧啶(G:m4T)错配在特定位置的45 bp DNA中进行切割的可能性。同时观察含有相同位置鸟嘌呤:胸腺嘧啶错配的45 bp DNA的切割情况,以确定提取物中碱基对结构与修复活性之间的关系。无细胞提取物对含有DiAP:T、AMAP:T和G:T碱基对的DNA切割情况相似。与已知的G:T错配切割模式相似,每种底物的产物都与两个切割位点一致,一个在错配胸腺嘧啶的5'端紧邻位置,另一个在3'端紧邻位置,且仅在含有错配胸腺嘧啶的链上。虽然含有O6 - 甲基鸟嘌呤:胸腺嘧啶(m6G:T)碱基对的DNA也能被切割,但含有G:m4T碱基对的DNA则不能,但经O6 - 甲基鸟嘌呤 - DNA甲基转移酶预处理后可变得可切割。提取物对含有DiAP:T的DNA的切割在存在含有G:T错配的未标记DNA时比存在含有A:T或G:A的DNA时或不存在竞争性DNA时少。我们认为作用于DiAP:T和/或AMAP:T碱基对的机制可能与人类G:T修复途径相同,可能是由Wiebauer和Jiricny [Wiebauer, K., & Jiricny, J. (1989) Nature 339, 234 - 236; Wiebauer, K., & Jiricny, J. (1990) Proc. Natl. Acad. Sci, U.S.A. 87, 5842 - 5845] 所描述的糖基化酶的作用引发的。(摘要截短至250字)

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