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人类端粒上 G 悬垂的产生的分子步骤及其在染色体末端保护中的功能。

Molecular steps of G-overhang generation at human telomeres and its function in chromosome end protection.

机构信息

WWAMI Medical Education Program, Washington State University, Spokane, WA 99210-1495, USA.

出版信息

EMBO J. 2010 Aug 18;29(16):2788-801. doi: 10.1038/emboj.2010.156. Epub 2010 Jul 16.

Abstract

Telomeric G-overhangs are required for the formation of the protective telomere structure and telomerase action. However, the mechanism controlling G-overhang generation at human telomeres is poorly understood. Here, we show that G-overhangs can undergo cell cycle-regulated changes independent of telomerase activity. G-overhangs at lagging telomeres are lengthened in S phase and then shortened in late S/G2 because of C-strand fill-in, whereas the sizes of G-overhangs at leading telomeres remain stable throughout S phase and are lengthened in G2/M. The final nucleotides at measurable C-strands are precisely defined throughout the cell cycle, indicating that C-strand resection is strictly regulated. We demonstrate that C-strand fill-in is mediated by DNA polymerase alpha (polalpha) and controlled by cyclin-dependent kinase 1 (CDK1). Inhibition of CDK1 leads to accumulation of lengthened G-overhangs and induces telomeric DNA damage response. Furthermore, depletion of hStn1 results in elongation of G-overhangs and an increase in telomeric DNA damage. Our results suggest that G-overhang generation at human telomeres is regulated by multiple tightly controlled processes and C-strand fill-in is under the control of polalpha and CDK1.

摘要

端粒 G 突出端对于形成保护性端粒结构和端粒酶的作用是必需的。然而,控制人类端粒上 G 突出端产生的机制还知之甚少。在这里,我们表明 G 突出端可以在不依赖端粒酶活性的情况下进行细胞周期调控变化。滞后端粒上的 G 突出端在 S 期延长,然后在晚期 S/G2 期由于 C 链填充而缩短,而先导端粒上 G 突出端的大小在整个 S 期保持稳定,并在 G2/M 期延长。整个细胞周期中可测量的 C 链末端核苷酸精确定义,表明 C 链切除受到严格调控。我们证明 C 链填充由 DNA 聚合酶α(polα)介导,并受细胞周期蛋白依赖性激酶 1(CDK1)控制。CDK1 的抑制导致延长的 G 突出端积累,并诱导端粒 DNA 损伤反应。此外,hStn1 的耗竭导致 G 突出端延长和端粒 DNA 损伤增加。我们的结果表明,人类端粒上 G 突出端的产生受多个严格控制的过程调节,C 链填充受 polα 和 CDK1 控制。

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