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A complex network of interactions governs DNA methylation at telomeric regions
DNA methylation modulates telomere function. In Arabidopsis thaliana, telomeric regions have a bimodal chromatin organization with unmethylated telomeres and methylated subtelomeres. To gain insight into this organization we have generated TAIR10-Tel, a modified version of the Arabidopsis reference...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860613/ https://www.ncbi.nlm.nih.gov/pubmed/35061900 http://dx.doi.org/10.1093/nar/gkac012 |
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author | Farrell, Colin Vaquero-Sedas, María I Cubiles, María D Thompson, Michael Vega-Vaquero, Alejandro Pellegrini, Matteo Vega-Palas, Miguel A |
author_facet | Farrell, Colin Vaquero-Sedas, María I Cubiles, María D Thompson, Michael Vega-Vaquero, Alejandro Pellegrini, Matteo Vega-Palas, Miguel A |
author_sort | Farrell, Colin |
collection | PubMed |
description | DNA methylation modulates telomere function. In Arabidopsis thaliana, telomeric regions have a bimodal chromatin organization with unmethylated telomeres and methylated subtelomeres. To gain insight into this organization we have generated TAIR10-Tel, a modified version of the Arabidopsis reference genome with additional sequences at most chromosome ends. TAIR10-Tel has allowed us to analyse DNA methylation at nucleotide resolution level in telomeric regions. We have analysed the wild-type strain and mutants that encode inactive versions of all currently known relevant methyltransferases involved in cytosine methylation. These analyses have revealed that subtelomeric DNA methylation extends 1 to 2 kbp from Interstitial Telomeric Sequences (ITSs) that abut or are very near to telomeres. However, DNA methylation drops at the telomeric side of the telomere-subtelomere boundaries and disappears at the inner part of telomeres. We present a comprehensive and integrative model for subtelomeric DNA methylation that should help to decipher the mechanisms that govern the epigenetic regulation of telomeres. This model involves a complex network of interactions between methyltransferases and subtelomeric DNA sequences. |
format | Online Article Text |
id | pubmed-8860613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88606132022-02-22 A complex network of interactions governs DNA methylation at telomeric regions Farrell, Colin Vaquero-Sedas, María I Cubiles, María D Thompson, Michael Vega-Vaquero, Alejandro Pellegrini, Matteo Vega-Palas, Miguel A Nucleic Acids Res Gene regulation, Chromatin and Epigenetics DNA methylation modulates telomere function. In Arabidopsis thaliana, telomeric regions have a bimodal chromatin organization with unmethylated telomeres and methylated subtelomeres. To gain insight into this organization we have generated TAIR10-Tel, a modified version of the Arabidopsis reference genome with additional sequences at most chromosome ends. TAIR10-Tel has allowed us to analyse DNA methylation at nucleotide resolution level in telomeric regions. We have analysed the wild-type strain and mutants that encode inactive versions of all currently known relevant methyltransferases involved in cytosine methylation. These analyses have revealed that subtelomeric DNA methylation extends 1 to 2 kbp from Interstitial Telomeric Sequences (ITSs) that abut or are very near to telomeres. However, DNA methylation drops at the telomeric side of the telomere-subtelomere boundaries and disappears at the inner part of telomeres. We present a comprehensive and integrative model for subtelomeric DNA methylation that should help to decipher the mechanisms that govern the epigenetic regulation of telomeres. This model involves a complex network of interactions between methyltransferases and subtelomeric DNA sequences. Oxford University Press 2022-01-21 /pmc/articles/PMC8860613/ /pubmed/35061900 http://dx.doi.org/10.1093/nar/gkac012 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Farrell, Colin Vaquero-Sedas, María I Cubiles, María D Thompson, Michael Vega-Vaquero, Alejandro Pellegrini, Matteo Vega-Palas, Miguel A A complex network of interactions governs DNA methylation at telomeric regions |
title | A complex network of interactions governs DNA methylation at telomeric regions |
title_full | A complex network of interactions governs DNA methylation at telomeric regions |
title_fullStr | A complex network of interactions governs DNA methylation at telomeric regions |
title_full_unstemmed | A complex network of interactions governs DNA methylation at telomeric regions |
title_short | A complex network of interactions governs DNA methylation at telomeric regions |
title_sort | complex network of interactions governs dna methylation at telomeric regions |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860613/ https://www.ncbi.nlm.nih.gov/pubmed/35061900 http://dx.doi.org/10.1093/nar/gkac012 |
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