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链断裂诱导的复制叉崩溃导致 C 环、C 突出和端粒重组。

Strand break-induced replication fork collapse leads to C-circles, C-overhangs and telomeric recombination.

机构信息

MOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, P. R. China.

School of Chemical Engineering and Technology, Guangdong Engineering Technical Research Center for Green Household Chemicals, Guangdong Industry Technical College, Guangzhou, P.R.China.

出版信息

PLoS Genet. 2019 Feb 4;15(2):e1007925. doi: 10.1371/journal.pgen.1007925. eCollection 2019 Feb.

Abstract

Telomerase-independent ALT (alternative lengthening of telomeres) cells are characterized by high frequency of telomeric homologous recombination (HR), C-rich extrachromosomal circles (C-circles) and C-rich terminal 5' overhangs (C-overhangs). However, underlying mechanism is poorly understood. Here, we show that both C-circle and C-overhang form when replication fork collapse is induced by strand break at telomeres. We find that endogenous DNA break predominantly occur on C-rich strand of telomeres in ALT cells, resulting in high frequency of replication fork collapse. While collapsed forks could be rescued by replication fork regression leading to telomeric homologous recombination, those unresolved are converted to C-circles and C-overhang at lagging and leading synthesized strand, respectively. Meanwhile, multiple hallmarks of ALT are provoked, suggesting that strand break-induced replication stress underlies ALT. These findings provide a molecular basis underlying telomeric HR and biogenesis of C-circle and C-overhang, thus implicating the specific mechanism to resolve strand break-induced replication defect at telomeres in ALT cells.

摘要

端粒酶独立的 ALT(端粒的替代性延长)细胞的特征是高频的端粒同源重组(HR)、富含 C 的染色体外环状 DNA(C-环)和富含 C 的端 5'突出端(C-突出端)。然而,其潜在的机制尚不清楚。在这里,我们表明当端粒处的链断裂诱导复制叉崩溃时,会形成 C-环和 C-突出端。我们发现内源性 DNA 断裂主要发生在 ALT 细胞中端粒富含 C 的链上,导致高频的复制叉崩溃。虽然崩溃的复制叉可以通过复制叉回退导致端粒同源重组来挽救,但那些未解决的问题会分别转化为滞后和领先合成链上的 C-环和 C-突出端。同时,ALT 的多个标志被引发,表明链断裂诱导的复制应激是 ALT 的基础。这些发现为端粒 HR 以及 C-环和 C-突出端的生物发生提供了分子基础,从而暗示了在 ALT 细胞中端粒处解决链断裂诱导的复制缺陷的特定机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/229e/6382176/ed25b38f8f44/pgen.1007925.g001.jpg

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