首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >3′ → 5′ Exonucleases of DNA Polymerases ? and δ Correct Base Analog Induced DNA Replication Errors on Opposite DNA Strands in Saccharomyces cerevisiae
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3′ → 5′ Exonucleases of DNA Polymerases ? and δ Correct Base Analog Induced DNA Replication Errors on Opposite DNA Strands in Saccharomyces cerevisiae

机译:DNA聚合酶的3'→5'外切核酸酶和δ正确碱基类似物在酿酒酵母中相反的DNA链上引起DNA复制错误

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The base analog 6- N -hydroxylaminopurine (HAP) induces bidirectional GC → AT and AT → GC transitions that are enhanced in DNA polymerase ? and δ 3′ → 5′ exonuclease-deficient yeast mutants, pol2-4 and pol3-01 , respectively. We have constructed a set of isogenic strains to determine whether the DNA polymerases δ and ? contribute equally to proofreading of replication errors provoked by HAP during leading and lagging strand DNA synthesis. Site-specific GC → AT and AT → GC transitions in a Pol→, pol2-4 or pol3-01 genetic background were scored as reversions of ura3 missense alleles. At each site, reversion was increased in only one proofreading-deficient mutant, either pol2-4 or pol3-01 , depending on the DNA strand in which HAP incorporation presumably occurred. Measurement of the HAP-induced reversion frequency of the ura3 alleles placed into chromosome III near to the defined active replication origin ARS306 in two orientations indicated that DNA polymerases ? and δ correct HAP-induced DNA replication errors on opposite DNA strands.
机译:碱基类似物6-N-羟基氨基嘌呤(HAP)诱导双向DNA聚合酶→GC和AT→AT→GC的转变。和δ3'→5'核酸外切酶缺陷型酵母突变体pol2-4和pol3-01。我们已经构建了一套等基因菌株,以确定DNA聚合酶δ和?同样有助于校对HAP在前导链和滞后链DNA合成过程中引起的复制错误。在Pol→,pol2-4或pol3-01遗传背景下,位点特异性GC→AT和AT→GC转换被记为ura3错义等位基因的回复。在每个位点,只有一个校对缺陷的突变体pol2-4或pol3-01的逆转录增加,这取决于可能发生HAP掺入的DNA链。在两个方向上测量HAP诱导的靠近定义的活性复制起点ARS306的III号染色体上的ura3等位基因的HAP诱导的回复频率,这表明DNA聚合酶α?和δ可纠正HAP诱导的相反DNA链上的DNA复制错误。

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