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用海拉细胞DNA聚合酶β和脱氧核糖核酸酶V组合进行切除修复和DNA合成。

Excision repair and DNA synthesis with a combination of HeLa DNA polymerase beta and DNase V.

作者信息

Mosbaugh D W, Linn S

出版信息

J Biol Chem. 1983 Jan 10;258(1):108-18.

PMID:6848490
Abstract

The ability of HeLa DNA polymerases to carry out DNA synthesis from incisions made by various endodeoxyribonucleases which recognize or form baseless sites in DNA was examined. DNA polymerase beta carried out limited strand displacement synthesis from 3'-hydroxyl nucleotide termini made by HeLa apurinic/apyrimidinic (AP) endonuclease II at the 5'-side of apurinic sites. Escherichia coli endonuclease III incises at the 3'-side of apurinic sites to produce nicks with 3'-deoxyribose termini which did not efficiently support DNA synthesis with beta-polymerase. However, these nicks could be activated to support limited DNA synthesis by HeLa AP endonuclease II, an enzyme which removes the baseless sugar phosphate from the 3'-termini, thus creating a one-nucleotide gap. With dGTP as the only nucleoside triphosphate present, the beta-polymerase catalyzed one-nucleotide DNA repair synthesis from those gaps which lacked dGMP. In contrast, HeLa DNA polymerase alpha was unreactive with all of the above incised DNA substrates. Larger patches of DNA synthesis were produced by nick translation from one-nucleotide gaps with HeLa DNA polymerase beta and HeLa DNase V. Moreover, incisions made by E. coli endonuclease III were activated to support DNA synthesis by the DNase V which removed the 3'-deoxyribose termini. HeLa DNase V also stimulated both the rate and extent of DNA synthesis by DNA polymerase beta from AP endonuclease II incisions. In this case the baseless sugar phosphate was removed from the 5'-termini, and nick translational synthesis occurred. Complete DNA excision repair of pyrimidine dimers was achieved with the beta-polymerase, DNase V, and DNA ligase from incisions made in UV-irradiated DNA by T4 UV endonuclease and HeLa AP endonuclease II. Such incisions produce a one-nucleotide gap containing 3'-hydroxyl nucleotide and 5'-thymine: thymidylate cyclobutane dimer termini. DNase V removes pyrimidine dimers primarily as a dinucleotide and then promotes nick translational DNA synthesis.

摘要

研究了海拉细胞DNA聚合酶从各种能识别或形成DNA中无碱基位点的内切脱氧核糖核酸酶所造成的切口处进行DNA合成的能力。DNA聚合酶β能从海拉细胞脱嘌呤/脱嘧啶(AP)内切核酸酶II在脱嘌呤位点5'侧产生的3'-羟基核苷酸末端进行有限的链置换合成。大肠杆菌内切核酸酶III在脱嘌呤位点的3'侧切割,产生带有3'-脱氧核糖末端的切口,这些切口不能有效地支持β-聚合酶进行DNA合成。然而,这些切口可被海拉细胞AP内切核酸酶II激活,以支持有限的DNA合成,该酶能从3'-末端去除无碱基的磷酸糖,从而形成一个单核苷酸缺口。当只有dGTP作为核苷三磷酸存在时,β-聚合酶能从那些缺乏dGMP的缺口中催化单核苷酸DNA修复合成。相比之下,海拉细胞DNA聚合酶α对上述所有切割后的DNA底物均无反应。用海拉细胞DNA聚合酶β和海拉细胞DNA酶V从单核苷酸缺口中进行切口平移可产生更大片段的DNA合成。此外,大肠杆菌内切核酸酶III造成的切口可被能去除3'-脱氧核糖末端的DNA酶V激活以支持DNA合成。海拉细胞DNA酶V还能刺激DNA聚合酶β从AP内切核酸酶II切口处进行DNA合成的速率和程度。在这种情况下,无碱基的磷酸糖从5'-末端被去除,从而发生切口平移合成。用β-聚合酶、DNA酶V和DNA连接酶可实现对紫外线照射的DNA经T4紫外线内切核酸酶和海拉细胞AP内切核酸酶II切割后嘧啶二聚体的完全DNA切除修复。这种切割产生一个包含3'-羟基核苷酸和5'-胸腺嘧啶:胸腺嘧啶环丁烷二聚体末端的单核苷酸缺口。DNA酶V主要以二核苷酸形式去除嘧啶二聚体,然后促进切口平移DNA合成。

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