School of Molecular Biosciences, Washington State University, Spokane, WA, USA.
Cell Cycle. 2012 Aug 15;11(16):3079-86. doi: 10.4161/cc.21472. Epub 2012 Aug 8.
Human telomeres contain single-stranded 3' G-overhangs that function in telomere end protection and telomerase action. Previously we have demonstrated that multiple steps involving C-strand end resection, telomerase elongation and C-strand fill-in contribute to G-overhang generation in telomerase-positive cancer cells. However, how G-overhangs are generated in telomerase-negative human somatic cells is unknown. Here, we report that C-strand fill-in is present at lagging-strand telomeres in telomerase-negative human cells but not at leading-strand telomeres, suggesting that C-strand fill-in is independent of telomerase extension of G-strand. We further show that while cyclin-dependent kinase 1 (CDK1) positively regulates C-strand fill-in, CDK1 unlikely regulates G-overhang generation at leading-strand telomeres. In addition, DNA polymerase α (Polα) association with telomeres is not altered upon CDK1 inhibition, suggesting that CDK1 does not control the loading of Polα to telomeres during fill-in. In summary, our results reveal that G-overhang generation at leading- and lagging-strand telomeres are regulated by distinct mechanisms in human cells.
端粒含有单链 3'G 突出端,在端粒末端保护和端粒酶作用中发挥功能。先前我们已经证明,涉及 C 链末端切除、端粒酶延伸和 C 链填充的多个步骤有助于端粒酶阳性癌细胞中 G 突出端的产生。然而,端粒酶阴性的人类体细胞中 G 突出端是如何产生的尚不清楚。在这里,我们报告在端粒酶阴性的人类细胞中,C 链填充存在于滞后链端粒上,但不存在于前导链端粒上,这表明 C 链填充独立于端粒酶延伸 G 链。我们进一步表明,虽然细胞周期蛋白依赖性激酶 1(CDK1)正向调节 C 链填充,但 CDK1 不太可能调节前导链端粒上的 G 突出端的产生。此外,CDK1 抑制后,与端粒的 DNA 聚合酶α(Polα)的关联没有改变,这表明 CDK1 不控制在填充过程中端粒 Polα 的加载。总之,我们的结果表明,在人类细胞中,前导链和滞后链端粒上 G 突出端的产生受不同机制的调节。