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Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile

Nucleosomes regulate many DNA-dependent processes by controlling the accessibility of DNA, and DNA sequences such as the poly-dA:dT element are known to affect nucleosome binding. We demonstrate that poly-dA:dT tracts form an asymmetric barrier to nucleosome movement in vivo, mediated by ATP-depende...

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Detalles Bibliográficos
Autores principales: de Boer, Carl G., Hughes, Timothy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212969/
https://www.ncbi.nlm.nih.gov/pubmed/25353956
http://dx.doi.org/10.1371/journal.pone.0110479
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author de Boer, Carl G.
Hughes, Timothy R.
author_facet de Boer, Carl G.
Hughes, Timothy R.
author_sort de Boer, Carl G.
collection PubMed
description Nucleosomes regulate many DNA-dependent processes by controlling the accessibility of DNA, and DNA sequences such as the poly-dA:dT element are known to affect nucleosome binding. We demonstrate that poly-dA:dT tracts form an asymmetric barrier to nucleosome movement in vivo, mediated by ATP-dependent chromatin remodelers. We theorize that nucleosome transit over poly-A elements is more energetically favourable in one direction, leading to an asymmetric arrangement of nucleosomes around these sequences. We demonstrate that different arrangements of poly-A and poly-T tracts result in very different outcomes for nucleosome occupancy in yeast, mouse, and human, and show that yeast takes advantage of this phenomenon in its promoter architecture.
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spelling pubmed-42129692014-11-05 Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile de Boer, Carl G. Hughes, Timothy R. PLoS One Research Article Nucleosomes regulate many DNA-dependent processes by controlling the accessibility of DNA, and DNA sequences such as the poly-dA:dT element are known to affect nucleosome binding. We demonstrate that poly-dA:dT tracts form an asymmetric barrier to nucleosome movement in vivo, mediated by ATP-dependent chromatin remodelers. We theorize that nucleosome transit over poly-A elements is more energetically favourable in one direction, leading to an asymmetric arrangement of nucleosomes around these sequences. We demonstrate that different arrangements of poly-A and poly-T tracts result in very different outcomes for nucleosome occupancy in yeast, mouse, and human, and show that yeast takes advantage of this phenomenon in its promoter architecture. Public Library of Science 2014-10-29 /pmc/articles/PMC4212969/ /pubmed/25353956 http://dx.doi.org/10.1371/journal.pone.0110479 Text en © 2014 de Boer, Hughes http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
de Boer, Carl G.
Hughes, Timothy R.
Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile
title Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile
title_full Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile
title_fullStr Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile
title_full_unstemmed Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile
title_short Poly-dA:dT Tracts Form an In Vivo Nucleosomal Turnstile
title_sort poly-da:dt tracts form an in vivo nucleosomal turnstile
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212969/
https://www.ncbi.nlm.nih.gov/pubmed/25353956
http://dx.doi.org/10.1371/journal.pone.0110479
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