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Studying telomere replication by Q-CO-FISH: the effect of telomestatin, a potent G-quadruplex ligand

机译:通过Q-CO-FISH研究端粒复制:端粒他汀(一种有效的G-四链体配体)的作用

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Telomere replication is a critical process for preserving genome integrity. The telomere replication fork proceeds unidirectionally from the last subtelomeric origin towards the end of the chromosome, replicating the 5'-3' G-rich strand by lagging mechanisms and the complementary C-rich strand by leading mechanisms. It has been proposed that the G-rich nature of telomeres may favor the formation of secondary structures such as G-quadruplexes duri ng replication and that specific mechanisms must prevent this to allow the fork to progress unimpeded. The potential of G-quadruplex formation by telomeric sequences has been clearly demonstrated in vitro but it is not known whether these structures form in vivo. We tested the effect of a potent and specific G-quadruplex ligand, telomestatin (TMS), on telomere replication using a novel quantitative approach applied to CO-FISH. We show that TMS, although it penetrates and persists within cells, does not affect telomere replication after short or long-term treatments of mouse embryonic fibroblasts. It does however affect the hybridization efficiency of FISH telomeric probes that recognize the G-rich strand. Our work illustrates the use of a novel technique to measure telomere replication efficiency and suggests that G-quadruplex ligands do not affect telomere replication in a non tumoral context.
机译:端粒复制是保持基因组完整性的关键过程。端粒复制叉从最后一个亚端粒起源单向延伸至染色体末端,通过滞后机制复制富含5'-3'G的链,并通过引导机制复制互补的富含C的链。有人提出,端粒的富含G的性质可能有利于复制过程中形成G-四链体之类的二级结构,并且必须采用特殊的机制来阻止这种现象,以使叉子不受阻碍地前进。在体外已经清楚地证明了由端粒序列形成G-四链体的潜力,但是尚不清楚这些结构是否在体内形成。我们使用适用于CO-FISH的新型定量方法,测试了一种有效且特异的G-四链体配体端粒他汀(TMS)对端粒复制的影响。我们显示,虽然TMS可以穿透并在细胞内持续存在,但在短期或长期治疗小鼠胚胎成纤维细胞后,不会影响端粒的复制。但是,它确实会影响识别富含G链的FISH端粒探针的杂交效率。我们的工作说明了使用一种新技术来测量端粒复制效率,并表明G-四链体配体在非肿瘤情况下不会影响端粒复制。

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