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人无细胞提取物对DNA中G:T和O6-甲基鸟嘌呤:T碱基错配处切口的位点特异性

Site specificity of incisions at G:T and O6-methylguanine:T base mismatches in DNA by human cell-free extracts.

作者信息

Day R S

机构信息

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

出版信息

Biochemistry. 1995 May 23;34(20):6869-75. doi: 10.1021/bi00020a034.

Abstract

Cell-free extract from human tumor cell line A1235 (lacking O6-methylguanine-DNA methyltransferase) was employed to compare incision at G:T base mispairs with that at O6-methylguanine (m6G):T pairs at two different sites (sites 20 and 25) in 45-bp heteroduplexes. To study the effect of neighboring bases on the activity(ies), the base pair immediately 5' to the mismatched G at each site was varied to provide four contexts: CpG:T, TpG:T, ApG:T, and GpG:T (and two analogous series for m6G:T pairs). At site 20, cell-free extract produced observable incision only in the 45-bp DNA with the G:T mispair in the CpG:T context, giving a product with incisions immediately 5' and 3' to the mismatched T. We observed incision of neither the strand containing the mismatched G nor the DNAs with the site 20 ApG:T, GpG:T, and TpG:T mismatches. By contrast, at site 25, incision specificity was different. All four G:T mismatched DNAs were incised, and the ApG:T-25, GpG:T-25, and TpG:T-25 DNAs were incised 1-3 bonds 3' to the mismatched T, while similar in other respects to the CpG:T-25 DNA, which showed a pattern like the CpG:T-20 DNA. CpG:T-20 specific incision activity in the extract was strongly inhibited by both CpG:T (sites 20 and 25) DNAs, but at least 10-fold more poorly by DNAs with Apg:T-25 and GpG:T-25 pairs.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用人肿瘤细胞系A1235(缺乏O6-甲基鸟嘌呤-DNA甲基转移酶)的无细胞提取物,比较45bp异源双链体中两个不同位点(位点20和25)处G:T碱基错配与O6-甲基鸟嘌呤(m6G):T碱基对处的切口情况。为研究相邻碱基对活性的影响,改变每个位点错配G紧邻的5'端碱基对,以提供四种序列环境:CpG:T、TpG:T、ApG:T和GpG:T(以及m6G:T碱基对的两个类似序列)。在位点20,无细胞提取物仅在CpG:T序列环境中含有G:T错配的45bp DNA中产生可观察到的切口,产生的产物在错配T的5'端和3'端紧邻处有切口。我们未观察到含有错配G的链以及具有位点20 ApG:T、GpG:T和TpG:T错配的DNA有切口。相比之下,在位点25,切口特异性不同。所有四种G:T错配的DNA都被切开,ApG:T-25、GpG:T-25和TpG:T-25 DNA在错配T的3'端1-3个键处被切开,在其他方面与CpG:T-25 DNA相似,后者显示出与CpG:T-20 DNA类似的模式。提取物中CpG:T-20特异性切口活性受到CpG:T(位点20和25)DNA的强烈抑制,但受到具有Apg:T-25和GpG:T-25碱基对的DNA的抑制作用至少低10倍。(摘要截短于250字)

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