TRF2形成t环的特征。

Leonid A Timashev, Titia De Lange
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摘要

T环被认为能使端粒免受DNA损伤信号传导和DSB修复途径的影响。T环的形成需要保护蛋白成分TRF2,它能抑制ATM信号传导和NHEJ。我们在此证实,在没有其他保护蛋白的情况下,仅 TRF2 就能形成 T 环。小鼠和人类细胞含有两种 TRF2 异构体,其中一种尚未定性。我们的研究表明,这两种异构体都能保护端粒并形成t-环。这两种异构体不受细胞周期调控,t-环存在于 G1、S 和 G2 期。 我们利用DNA包裹缺陷的TRF2 Topless突变体,证实了它不能形成t环和抑制ATM。然而,由于该突变体在抑制 NHEJ 和端粒定位方面也存在缺陷,拓扑变化在端粒保护中的作用仍不清楚。 最后,我们发现 Rad51 不会影响 t 环频率或端粒保护。因此,应该探索TRF2如何形成t-环的其他模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Characterization of t-loop formation by TRF2.

T-loops are thought to hide telomeres from DNA damage signaling and DSB repair pathways. T-loop formation requires the shelterin component TRF2, which represses ATM signaling and NHEJ. Here we establish that TRF2 alone, in the absence of other shelterin proteins can form t-loops. Mouse and human cells contain two isoforms of TRF2, one of which is uncharacterized. We show that both isoforms protect telomeres and form t-loops. The isoforms are not cell cycle regulated and t-loops are present in G1, S, and G2.  Using the DNA wrapping deficient TRF2 Topless mutant, we confirm its inability to form t-loops and repress ATM. However, since the mutant is also defective in repression of NHEJ and telomeric localization, the role of topological changes in telomere protection remains unclear.  Finally, we show that Rad51 does not affect t-loop frequencies or telomere protection. Therefore, alternative models for how TRF2 forms t-loops should be explored.

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