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酵母CDC9基因编码DNA连接酶I的一种核形式和一种线粒体形式。

The yeast CDC9 gene encodes both a nuclear and a mitochondrial form of DNA ligase I.

作者信息

Willer M, Rainey M, Pullen T, Stirling C J

机构信息

School of Biological Sciences 2.205 Stopford Building University of Manchester Oxford Road, Manchester, M13 9PT, UK.

出版信息

Curr Biol. 1999 Oct 7;9(19):1085-94. doi: 10.1016/s0960-9822(99)80477-1.

DOI:10.1016/s0960-9822(99)80477-1
PMID:10531002
Abstract

BACKGROUND

The yeast CDC9 gene encodes a DNA ligase I activity required during nuclear DNA replication to ligate the Okazaki fragments formed when the lagging DNA strand is synthesised. The only other DNA ligase predicted from the yeast genome sequence, DNL4/LIG4, is specifically involved in a non-homologous DNA end-joining reaction. What then is the source of the DNA ligase activity required for replication of the yeast mitochondrial genome?

RESULTS

We report that CDC9 encodes two distinct polypeptides expressed from consecutive in-frame AUG codons. Translational initiation at these two sites gives rise to polypeptides differing by a 23 residue amino-terminal extension, which corresponds to a functional mitochondrial pre-sequence sufficient to direct import into yeast mitochondria. Initiation at the first AUG codon results in a 755 amino-acid polypeptide that is imported into mitochondria, whereupon the pre-sequence is proteolytically removed to yield the mature mitochondrial form of Cdc9p. Initiation at the second AUG codon produces a 732 amino-acid polypeptide, which is localised to the nucleus. Cells expressing only the nuclear isoform were found to be specifically defective in the maintenance of the mitochondrial genome.

CONCLUSIONS

CDC9 encodes two distinct forms of DNA ligase I. The first is targeted to the mitochondrion and is required for propagation and maintenance of mitochondrial DNA, the second localises to the nucleus and is sufficient for the essential cell-division function associated with this gene.

摘要

背景

酵母CDC9基因编码一种DNA连接酶I活性,该活性在核DNA复制过程中是连接滞后DNA链合成时形成的冈崎片段所必需的。从酵母基因组序列预测的唯一另一种DNA连接酶DNL4/LIG4,专门参与非同源DNA末端连接反应。那么酵母线粒体基因组复制所需的DNA连接酶活性的来源是什么呢?

结果

我们报告称,CDC9编码从连续的框内AUG密码子表达的两种不同多肽。在这两个位点的翻译起始产生了相差23个残基的氨基末端延伸的多肽,这对应于一个足以指导导入酵母线粒体的功能性线粒体前序列。在第一个AUG密码子处起始产生一个755个氨基酸的多肽,该多肽被导入线粒体,随后前序列被蛋白酶水解去除,产生成熟的线粒体形式的Cdc9p。在第二个AUG密码子处起始产生一个732个氨基酸的多肽,该多肽定位于细胞核。发现仅表达核异构体的细胞在维持线粒体基因组方面存在特异性缺陷。

结论

CDC9编码两种不同形式的DNA连接酶I。第一种靶向线粒体,是线粒体DNA复制和维持所必需的,第二种定位于细胞核,足以实现与该基因相关的基本细胞分裂功能。

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