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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 cel...

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Autores principales: Timashev, Leonid A., De Lange, Titia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529409/
https://www.ncbi.nlm.nih.gov/pubmed/32564646
http://dx.doi.org/10.1080/19491034.2020.1783782
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author Timashev, Leonid A.
De Lange, Titia
author_facet Timashev, Leonid A.
De Lange, Titia
author_sort Timashev, Leonid A.
collection PubMed
description 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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spelling pubmed-75294092020-10-13 Characterization of t-loop formation by TRF2 Timashev, Leonid A. De Lange, Titia Nucleus Research Paper 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. Taylor & Francis 2020-07-14 /pmc/articles/PMC7529409/ /pubmed/32564646 http://dx.doi.org/10.1080/19491034.2020.1783782 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Timashev, Leonid A.
De Lange, Titia
Characterization of t-loop formation by TRF2
title Characterization of t-loop formation by TRF2
title_full Characterization of t-loop formation by TRF2
title_fullStr Characterization of t-loop formation by TRF2
title_full_unstemmed Characterization of t-loop formation by TRF2
title_short Characterization of t-loop formation by TRF2
title_sort characterization of t-loop formation by trf2
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529409/
https://www.ncbi.nlm.nih.gov/pubmed/32564646
http://dx.doi.org/10.1080/19491034.2020.1783782
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