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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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 |
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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 |
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