Cargando…

The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin

Heterochromatic regions render the replication process particularly difficult due to the high level of chromatin compaction and the presence of repeated DNA sequences. In humans, replication through pericentromeric heterochromatin requires the binding of a complex formed by the telomeric factor TRF2...

Descripción completa

Detalles Bibliográficos
Autores principales: Bauwens, Serge, Lototska, Liudmyla, Koundrioukoff, Stephane, Debatisse, Michelle, Ye, Jing, Gilson, Eric, Mendez-Bermudez, Aaron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063955/
https://www.ncbi.nlm.nih.gov/pubmed/33804994
http://dx.doi.org/10.3390/life11040267
_version_ 1783682044263399424
author Bauwens, Serge
Lototska, Liudmyla
Koundrioukoff, Stephane
Debatisse, Michelle
Ye, Jing
Gilson, Eric
Mendez-Bermudez, Aaron
author_facet Bauwens, Serge
Lototska, Liudmyla
Koundrioukoff, Stephane
Debatisse, Michelle
Ye, Jing
Gilson, Eric
Mendez-Bermudez, Aaron
author_sort Bauwens, Serge
collection PubMed
description Heterochromatic regions render the replication process particularly difficult due to the high level of chromatin compaction and the presence of repeated DNA sequences. In humans, replication through pericentromeric heterochromatin requires the binding of a complex formed by the telomeric factor TRF2 and the helicase RTEL1 in order to relieve topological barriers blocking fork progression. Since TRF2 is known to bind the Origin Replication Complex (ORC), we hypothesized that this factor could also play a role at the replication origins (ORI) of these heterochromatin regions. By performing DNA combing analysis, we found that the ORI density is higher within pericentromeric satellite DNA repeats than within bulk genomic DNA and decreased upon TRF2 downregulation. Moreover, we showed that TRF2 and ORC2 interact in pericentromeric DNA, providing a mechanism by which TRF2 is involved in ORI activity. Altogether, our findings reveal an essential role for TRF2 in pericentromeric heterochromatin replication by regulating both replication initiation and elongation.
format Online
Article
Text
id pubmed-8063955
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-80639552021-04-24 The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin Bauwens, Serge Lototska, Liudmyla Koundrioukoff, Stephane Debatisse, Michelle Ye, Jing Gilson, Eric Mendez-Bermudez, Aaron Life (Basel) Article Heterochromatic regions render the replication process particularly difficult due to the high level of chromatin compaction and the presence of repeated DNA sequences. In humans, replication through pericentromeric heterochromatin requires the binding of a complex formed by the telomeric factor TRF2 and the helicase RTEL1 in order to relieve topological barriers blocking fork progression. Since TRF2 is known to bind the Origin Replication Complex (ORC), we hypothesized that this factor could also play a role at the replication origins (ORI) of these heterochromatin regions. By performing DNA combing analysis, we found that the ORI density is higher within pericentromeric satellite DNA repeats than within bulk genomic DNA and decreased upon TRF2 downregulation. Moreover, we showed that TRF2 and ORC2 interact in pericentromeric DNA, providing a mechanism by which TRF2 is involved in ORI activity. Altogether, our findings reveal an essential role for TRF2 in pericentromeric heterochromatin replication by regulating both replication initiation and elongation. MDPI 2021-03-24 /pmc/articles/PMC8063955/ /pubmed/33804994 http://dx.doi.org/10.3390/life11040267 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Bauwens, Serge
Lototska, Liudmyla
Koundrioukoff, Stephane
Debatisse, Michelle
Ye, Jing
Gilson, Eric
Mendez-Bermudez, Aaron
The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin
title The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin
title_full The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin
title_fullStr The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin
title_full_unstemmed The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin
title_short The Telomeric Protein TRF2 Regulates Replication Origin Activity within Pericentromeric Heterochromatin
title_sort telomeric protein trf2 regulates replication origin activity within pericentromeric heterochromatin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063955/
https://www.ncbi.nlm.nih.gov/pubmed/33804994
http://dx.doi.org/10.3390/life11040267
work_keys_str_mv AT bauwensserge thetelomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT lototskaliudmyla thetelomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT koundrioukoffstephane thetelomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT debatissemichelle thetelomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT yejing thetelomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT gilsoneric thetelomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT mendezbermudezaaron thetelomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT bauwensserge telomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT lototskaliudmyla telomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT koundrioukoffstephane telomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT debatissemichelle telomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT yejing telomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT gilsoneric telomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin
AT mendezbermudezaaron telomericproteintrf2regulatesreplicationoriginactivitywithinpericentromericheterochromatin