Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Farrell, Colin, Vaquero-Sedas, María I, Cubiles, María D, Thompson, Michael, Vega-Vaquero, Alejandro, Pellegrini, Matteo, Vega-Palas, Miguel A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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
_version_ 1784654715699593216
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
work_keys_str_mv AT farrellcolin acomplexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT vaquerosedasmariai acomplexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT cubilesmariad acomplexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT thompsonmichael acomplexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT vegavaqueroalejandro acomplexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT pellegrinimatteo acomplexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT vegapalasmiguela acomplexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT farrellcolin complexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT vaquerosedasmariai complexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT cubilesmariad complexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT thompsonmichael complexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT vegavaqueroalejandro complexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT pellegrinimatteo complexnetworkofinteractionsgovernsdnamethylationattelomericregions
AT vegapalasmiguela complexnetworkofinteractionsgovernsdnamethylationattelomericregions