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端粒合成和延长的不同模式促成了端粒的替代延长。

Distinct modes of telomere synthesis and extension contribute to Alternative Lengthening of Telomeres.

作者信息

Lu Robert, Nelson Christopher B, Rogers Samuel, Cesare Anthony J, Sobinoff Alexander P, Pickett Hilda A

机构信息

Telomere Length Regulation Unit, Children's Medical Research Institute, University of Sydney, Westmead, NSW, Australia.

Genome Integrity Unit, Children's Medical Research Institute, University of Sydney, Westmead, NSW, Australia.

出版信息

iScience. 2023 Dec 11;27(1):108655. doi: 10.1016/j.isci.2023.108655. eCollection 2024 Jan 19.

Abstract

Alternative lengthening of telomeres (ALT) is a homology-directed repair mechanism that becomes activated in a subset of cancers to maintain telomere length. One of the defining features of ALT cells is the prevalence of extrachromosomal telomeric repeat (ECTR) DNA. Here, we identify that ALT cells engage in two modes of telomere synthesis. Non-productive telomere synthesis occurs during the G2 phase of the cell cycle and is characterized by newly synthesized internal telomeric regions that are not retained in the subsequent G1, coinciding with an induction of ECTR DNA. Productive telomere synthesis occurs specifically during the transition from G2 to mitosis and is defined as the extension of the telomere termini. While many proteins associated with break-induced telomere synthesis function in both non-productive and productive telomere synthesis, POLH specifically promotes productive telomere lengthening and suppresses non-productive telomere synthesis. These findings delineate the mechanism and cell cycle regulation of ALT-mediated telomere synthesis and extension.

摘要

端粒替代延长(ALT)是一种同源定向修复机制,在一部分癌症中被激活以维持端粒长度。ALT细胞的一个显著特征是染色体外端粒重复序列(ECTR)DNA的普遍存在。在此,我们发现ALT细胞参与两种端粒合成模式。非生产性端粒合成发生在细胞周期的G2期,其特征是新合成的内部端粒区域在随后的G1期未被保留,这与ECTR DNA的诱导同时发生。生产性端粒合成特别发生在从G2期到有丝分裂的转变过程中,被定义为端粒末端的延伸。虽然许多与断裂诱导的端粒合成相关的蛋白质在非生产性和生产性端粒合成中都起作用,但POLH特别促进生产性端粒延长并抑制非生产性端粒合成。这些发现阐明了ALT介导的端粒合成和延长的机制以及细胞周期调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa7a/10783591/e11860ac1b3a/fx1.jpg

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