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首页> 外文期刊>Nucleic Acids Research >Functional analysis of subcellular localization and protein–protein interaction sequences in the essential DNA ligase I protein of fission yeast
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Functional analysis of subcellular localization and protein–protein interaction sequences in the essential DNA ligase I protein of fission yeast

机译:裂殖酵母基本DNA连接酶I蛋白中亚细胞定位和蛋白-蛋白相互作用序列的功能分析

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摘要

DNA ligase I (Lig I) has key roles in chromosomal DNA replication and repair in the eukaryotic cell nucleus. In the budding yeast Saccharomyces cerevisiae the Lig I enzyme Cdc9p is also required for mitochondrial DNA replication and repair. In this report, dual nuclear–mitochondrial localization is demonstrated to be a property of the essential Lig I enzyme Cdc17 from the distantly related fission yeast Schizosaccharomyces pombe. Expression of nuclear and mitochondrial forms of Cdc17 from separate genes shows that, whereas expression of either protein alone is insufficient to restore viability to cells lacking endogenous Cdc17, co-expression restores full viability. In the nucleus, Lig I interacts with the sliding clamp proliferating cell nuclear antigen (PCNA) via a conserved PCNA interacting sequence motif known as a PIP box. Deletion of the PIP motif from the N-terminus of the nuclear form of Cdc17 fails to abolish Cdc17 function, indicating that PCNA binding by Cdc17 is not an absolute requirement for completion of S-phase.
机译:DNA连接酶I(图I)在染色体DNA复制和真核细胞核修复中起关键作用。在萌芽的酿酒酵母中,线粒体DNA复制和修复也需要Lig I酶Cdc9p。在本报告中,双核线粒体定位被证明是来自远缘裂变酵母裂殖酵母的必需Lig I酶Cdc17的特性。 Cdc17的核和线粒体形式来自不同基因的表达表明,尽管单独表达两种蛋白质不足以恢复缺乏内源性Cdc17的细胞的活力,但共表达可恢复全部活力。在细胞核中,Lig I通过保守的PCNA相互作用序列基序(称为PIP盒)与滑动钳增殖细胞核抗原(PCNA)相互作用。从Cdc17核形式的N末端删除PIP基序无法取消Cdc17功能,这表明通过Cdc17进行PCNA结合并不是完成S期的绝对必要条件。

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