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RTEL1 dismantles T loops and counteracts telomeric G4-DNA to maintain telomere integrity

机译:RTEL1拆除T环并抵消端粒G4-DNA以维持端粒完整性

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摘要

T loops and telomeric G-quadruplex (G4) DNA structures pose a potential threat to genome stability and must be dismantled to permit efficient telomere replication. Here we implicate the helicase RTEL1 in the removal of telomeric DNA secondary structures, which is essential for preventing telomere fragility and loss. In the absence of RTEL1, T loops are inappropriately resolved by the SLX4 nuclease complex, resulting in loss of the telomere as a circle. Depleting SLX4 or blocking DNA replication abolished telomere circles (TCs) and rescued telomere loss in RTEL1 ~(-/-) cells but failed to suppress telomere fragility. Conversely, stabilization of telomeric G4-DNA or loss of BLM dramatically enhanced telomere fragility in RTEL1-deficient cells but had no impact on TC formation or telomere loss. We propose that RTEL1 performs two distinct functions at telomeres: it disassembles T loops and also counteracts telomeric G4-DNA structures, which together ensure the dynamics and stability of the telomere.
机译:T环和端粒G-四链体(G4)DNA结构对基因组稳定性构成潜在威胁,必须拆除才能有效地复制端粒。在这里,我们暗示解旋酶RTEL1去除端粒DNA二级结构,这对于防止端粒的脆性和丢失至关重要。在缺少RTEL1的情况下,SLX4核酸酶复合物不能正确解析T环,从而导致端粒丧失为一个圆形。耗尽SLX4或阻止DNA复制消除了端粒环(TCs),并挽救了RTEL1〜(-/-)细胞中的端粒丢失,但未能抑制端粒的脆性。相反,端粒G4-DNA的稳定或BLM的丧失显着增强了RTEL1缺陷细胞中端粒的脆性,但对TC的形成或端粒的丢失没有影响。我们建议RTEL1在端粒上执行两个不同的功能:它拆解T环,还抵消端粒G4-DNA结构,这一起确保端粒的动力学和稳定性。

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