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Biochemical and genetic characterization of the DNA ligase encoded by Saccharomyces cerevisiae open reading frame YOR005c, a homolog of mammalian DNA ligase IV

机译:酿酒酵母开放阅读框YOR005c(哺乳动物DNA连接酶IV的同源物)编码的DNA连接酶的生化和遗传特征

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Here we demonstrate that the Saccharomyces cerevisiae DNA ligase activity, which we previously designated DNA ligase II, is encoded by the genomic DNA sequence YOR005c. Based on its homology with mammalian LIG4, this yeast gene has been named DNL4 and the enzyme activity renamed Dnl4. In agreement with others, we find that DNL4 is not required for vegetative growth but is involved in the repair of DNA double-strand breaks by non-homologous end joining. In contrast to a previous report, we find that a dnl4 null mutation has no effect on sporulation efficiency, indicating that Dnl4 is not required for proper meiotic chromosome behavior or subsequent ascosporogenesis in yeast. Disruption of the DNL4 gene in one strain, M1-2B, results in temperature-sensitive vegetative growth. At the restrictive temperature, mutant cells progressively lose viability and accumulate small, nucleated and non-dividing daughter cells which remain attached to the mother cell. This novel temperature-sensitive phenotype is complemented by retransformation with a plasmidborne DNL4 gene. Thus, we conclude that the abnormal growth of the dnl4 mutant strain is a synthetic phenotype resulting from Dnl4 deficiency in combination with undetermined genetic factors in the M1-2B strain background.
机译:在这里,我们证明了酿酒酵母DNA连接酶的活性,我们以前称为DNA连接酶II,是由基因组DNA序列YOR005c编码的。基于其与哺乳动物LIG4的同源性,该酵母基因已被命名为DNL4,酶活性被重命名为Dnl4。与他人达成共识,我们发现营养生长不需要DNL4,但它通过非同源末端连接参与DNA双链断裂的修复。与以前的报告相反,我们发现dnl4无效突变对孢子形成效率没有影响,表明Dnl4并不是适当的减数分裂染色体行为或随后的酵母中孢子发生所必需的。一种菌株M1-2B中DNL4基因的破坏导致对温度敏感的营养生长。在限制性温度下,突变细胞逐渐丧失活力,并积累小的,有核的和不分裂的子细胞,这些子细胞仍与母细胞保持连接。这种新的温度敏感性表型通过质粒转化的DNL4基因的再转化得到补充。因此,我们得出结论,dnl4突变菌株的异常生长是由Dnl4缺乏与M1-2B菌株背景中不确定的遗传因素结合而产生的合成表型。

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