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体外c-Ha-ras基因热点区域中核苷酸掺入及延伸与8-羟基鸟嘌呤(7,8-二氢-8-氧代鸟嘌呤)配对情况的比较

Comparison of incorporation and extension of nucleotides in vitro opposite 8-hydroxyguanine (7,8-dihydro-8-oxoguanine) in hot spots of the c-Ha-ras gene.

作者信息

Kamiya H, Murata-Kamiya N, Fujimuro M, Kido K, Inoue H, Nishimura S, Masutani C, Hanaoka F, Ohtsuka E

机构信息

Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo.

出版信息

Jpn J Cancer Res. 1995 Mar;86(3):270-6. doi: 10.1111/j.1349-7006.1995.tb03050.x.

Abstract

DNA templates with 8-hydroxyguanine (7,8-dihydro-8-oxoguanine, oh8Gua) at a site corresponding to the first or second position of codon 12 of the c-Ha-ras gene were prepared, and the nucleotides inserted opposite the modified base were compared. The Klenow fragment (KF) of Escherichia coli DNA polymerase I inserted C opposite oh8Gua at both positions. Taq DNA polymerase incorporated C and A opposite oh8Gua, and the ratio of C to A was higher at the first position than at the second position. DNA polymerase alpha (pol alpha) inserted A and C at the first position, and A at the second position of codon 12, indicating that the ratio of C to A was higher at the first position. Moreover, we studied the extensions of bases paired with oh8Gua by DNA polymerases with or without 3'-5' exonuclease activity. G and T opposite oh8Gua were removed, and subsequently C was inserted by KF. We found that an oh8Gua:A pair was recognized by the exonuclease activity of the enzyme and that A was partially substituted by C. On the other hand, pol alpha extended only C and A opposite oh8Gua. No difference was observed with oh8Gua at the two positions. These results indicate that the ratio of nucleotides incorporated opposite oh8Gua depends on the sequence context, while there is no particular difference in the extension of base pairs involving oh8Gua by DNA polymerases.

摘要

制备了在与c-Ha-ras基因第12密码子的第一位或第二位相对应的位点含有8-羟基鸟嘌呤(7,8-二氢-8-氧代鸟嘌呤,oh8Gua)的DNA模板,并比较了在修饰碱基对面插入的核苷酸。大肠杆菌DNA聚合酶I的Klenow片段(KF)在两个位置都在oh8Gua对面插入C。Taq DNA聚合酶在oh8Gua对面掺入C和A,且在第一位C与A的比例高于第二位。DNA聚合酶α(polα)在第12密码子的第一位插入A和C,在第二位插入A,表明在第一位C与A的比例更高。此外,我们研究了具有或不具有3'-5'外切核酸酶活性的DNA聚合酶对与oh8Gua配对的碱基的延伸情况。oh8Gua对面的G和T被去除,随后KF插入C。我们发现oh8Gua:A对被该酶的外切核酸酶活性识别,且A部分被C取代。另一方面,polα仅在oh8Gua对面延伸C和A。在两个位置的oh8Gua未观察到差异。这些结果表明,在oh8Gua对面掺入的核苷酸比例取决于序列背景,而DNA聚合酶对涉及oh8Gua的碱基对的延伸没有特别差异。

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