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Ruler elements in chromatin remodelers set nucleosome array spacing and phasing
Arrays of regularly spaced nucleosomes dominate chromatin and are often phased by alignment to reference sites like active promoters. How the distances between nucleosomes (spacing), and between phasing sites and nucleosomes are determined remains unclear, and specifically, how ATP-dependent chromat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163753/ https://www.ncbi.nlm.nih.gov/pubmed/34050140 http://dx.doi.org/10.1038/s41467-021-23015-0 |
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author | Oberbeckmann, Elisa Niebauer, Vanessa Watanabe, Shinya Farnung, Lucas Moldt, Manuela Schmid, Andrea Cramer, Patrick Peterson, Craig L. Eustermann, Sebastian Hopfner, Karl-Peter Korber, Philipp |
author_facet | Oberbeckmann, Elisa Niebauer, Vanessa Watanabe, Shinya Farnung, Lucas Moldt, Manuela Schmid, Andrea Cramer, Patrick Peterson, Craig L. Eustermann, Sebastian Hopfner, Karl-Peter Korber, Philipp |
author_sort | Oberbeckmann, Elisa |
collection | PubMed |
description | Arrays of regularly spaced nucleosomes dominate chromatin and are often phased by alignment to reference sites like active promoters. How the distances between nucleosomes (spacing), and between phasing sites and nucleosomes are determined remains unclear, and specifically, how ATP-dependent chromatin remodelers impact these features. Here, we used genome-wide reconstitution to probe how Saccharomyces cerevisiae ATP-dependent remodelers generate phased arrays of regularly spaced nucleosomes. We find that remodelers bear a functional element named the ‘ruler’ that determines spacing and phasing in a remodeler-specific way. We use structure-based mutagenesis to identify and tune the ruler element residing in the Nhp10 and Arp8 modules of the INO80 remodeler complex. Generally, we propose that a remodeler ruler regulates nucleosome sliding direction bias in response to (epi)genetic information. This finally conceptualizes how remodeler-mediated nucleosome dynamics determine stable steady-state nucleosome positioning relative to other nucleosomes, DNA bound factors, DNA ends and DNA sequence elements. |
format | Online Article Text |
id | pubmed-8163753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81637532021-06-11 Ruler elements in chromatin remodelers set nucleosome array spacing and phasing Oberbeckmann, Elisa Niebauer, Vanessa Watanabe, Shinya Farnung, Lucas Moldt, Manuela Schmid, Andrea Cramer, Patrick Peterson, Craig L. Eustermann, Sebastian Hopfner, Karl-Peter Korber, Philipp Nat Commun Article Arrays of regularly spaced nucleosomes dominate chromatin and are often phased by alignment to reference sites like active promoters. How the distances between nucleosomes (spacing), and between phasing sites and nucleosomes are determined remains unclear, and specifically, how ATP-dependent chromatin remodelers impact these features. Here, we used genome-wide reconstitution to probe how Saccharomyces cerevisiae ATP-dependent remodelers generate phased arrays of regularly spaced nucleosomes. We find that remodelers bear a functional element named the ‘ruler’ that determines spacing and phasing in a remodeler-specific way. We use structure-based mutagenesis to identify and tune the ruler element residing in the Nhp10 and Arp8 modules of the INO80 remodeler complex. Generally, we propose that a remodeler ruler regulates nucleosome sliding direction bias in response to (epi)genetic information. This finally conceptualizes how remodeler-mediated nucleosome dynamics determine stable steady-state nucleosome positioning relative to other nucleosomes, DNA bound factors, DNA ends and DNA sequence elements. Nature Publishing Group UK 2021-05-28 /pmc/articles/PMC8163753/ /pubmed/34050140 http://dx.doi.org/10.1038/s41467-021-23015-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Oberbeckmann, Elisa Niebauer, Vanessa Watanabe, Shinya Farnung, Lucas Moldt, Manuela Schmid, Andrea Cramer, Patrick Peterson, Craig L. Eustermann, Sebastian Hopfner, Karl-Peter Korber, Philipp Ruler elements in chromatin remodelers set nucleosome array spacing and phasing |
title | Ruler elements in chromatin remodelers set nucleosome array spacing and phasing |
title_full | Ruler elements in chromatin remodelers set nucleosome array spacing and phasing |
title_fullStr | Ruler elements in chromatin remodelers set nucleosome array spacing and phasing |
title_full_unstemmed | Ruler elements in chromatin remodelers set nucleosome array spacing and phasing |
title_short | Ruler elements in chromatin remodelers set nucleosome array spacing and phasing |
title_sort | ruler elements in chromatin remodelers set nucleosome array spacing and phasing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163753/ https://www.ncbi.nlm.nih.gov/pubmed/34050140 http://dx.doi.org/10.1038/s41467-021-23015-0 |
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