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The Ku Heterodimer Performs Separable Activities at Double-Strand Breaks and Chromosome Termini

机译:Ku异二聚体在双链断裂和染色体Termini上执行独立的活动

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摘要

The Ku heterodimer functions at two kinds of DNA ends: telomeres and double-strand breaks. The role that Ku plays at these two classes of termini must be distinct, because Ku is required for accurate and efficient joining of double-strand breaks while similar DNA repair events are normally prohibited at chromosome ends. Toward defining these functional differences, we have identified eight mutations in the large subunit of the Saccharomyces cerevisiae Ku heterodimer (YKU80) which retain the ability to repair double-strand breaks but are severely impaired for chromosome end protection. Detailed characterization of these mutations, referred to as yku80tel alleles, has revealed that Ku performs functionally distinct activities at subtelomeric chromatin versus the end of the chromosome, and these activities are separable from Ku's role in telomere length regulation. While at the chromosome terminus, we propose that Ku participates in two different activities: it facilitates telomerase-mediated G-strand synthesis, thereby contributing to telomere length regulation, and it separately protects against resection of the C-strand, thereby contributing to protection of chromosome termini. Furthermore, we propose that the Ku heterodimer performs discrete sets of functions at chromosome termini and at duplex subtelomeric chromatin, via separate interactions with these two locations. Based on homology modeling with the human Ku structure, five of the yku80tel alleles mutate residues that are conserved between the yeast and human Ku80 proteins, suggesting that these mutations probe activities that are shared between yeast and humans.
机译:Ku异二聚体在两种DNA末端起作用:端粒和双链断裂。 Ku在这两类末端中所起的作用必须是不同的,因为Ku是精确有效地连接双链断裂所必需的,而通常在染色体末端则禁止类似的DNA修复事件。为了定义这些功能差异,我们在酿酒酵母Ku异二聚体(YKU80)的大亚基中鉴定了8个突变,这些突变保留了修复双链断裂的能力,但严重损害了染色体末端保护功能。对这些突变的详细表征,称为yku80 tel 等位基因,揭示了Ku在端粒亚染色质上的功能与染色体末端不同,而这些功能与Ku在端粒长度调节中的作用是可分离的。我们建议在染色体末端,Ku参与两种不同的活动:它促进端粒酶介导的G链合成,从而促进端粒长度调节,并分别防止C链的切除,从而有助于保护C.链。染色体末端。此外,我们建议Ku异二聚体通过与这两个位置的单独相互作用在染色体末端和双链亚端粒染色质上执行离散功能集。基于与人类Ku结构的同源性建模,yku80 tel 等位基因中的五个突变了酵母和人类Ku80蛋白之间保守的残基,这表明这些突变可探测酵母和人类之间共有的活性。

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