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Global reorganization of budding yeast chromosome conformation in different physiological conditions
The organization of the genome is nonrandom and important for correct function. Specifically, the nuclear envelope plays a critical role in gene regulation. It generally constitutes a repressive environment, but several genes, including the GAL locus in budding yeast, are recruited to the nuclear pe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748577/ https://www.ncbi.nlm.nih.gov/pubmed/26811423 http://dx.doi.org/10.1083/jcb.201507069 |
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author | Dultz, Elisa Tjong, Harianto Weider, Elodie Herzog, Mareike Young, Barry Brune, Christiane Müllner, Daniel Loewen, Christopher Alber, Frank Weis, Karsten |
author_facet | Dultz, Elisa Tjong, Harianto Weider, Elodie Herzog, Mareike Young, Barry Brune, Christiane Müllner, Daniel Loewen, Christopher Alber, Frank Weis, Karsten |
author_sort | Dultz, Elisa |
collection | PubMed |
description | The organization of the genome is nonrandom and important for correct function. Specifically, the nuclear envelope plays a critical role in gene regulation. It generally constitutes a repressive environment, but several genes, including the GAL locus in budding yeast, are recruited to the nuclear periphery on activation. Here, we combine imaging and computational modeling to ask how the association of a single gene locus with the nuclear envelope influences the surrounding chromosome architecture. Systematic analysis of an entire yeast chromosome establishes that peripheral recruitment of the GAL locus is part of a large-scale rearrangement that shifts many chromosomal regions closer to the nuclear envelope. This process is likely caused by the presence of several independent anchoring points. To identify novel factors required for peripheral anchoring, we performed a genome-wide screen and demonstrated that the histone acetyltransferase SAGA and the activity of histone deacetylases are needed for this extensive gene recruitment to the nuclear periphery. |
format | Online Article Text |
id | pubmed-4748577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47485772016-08-01 Global reorganization of budding yeast chromosome conformation in different physiological conditions Dultz, Elisa Tjong, Harianto Weider, Elodie Herzog, Mareike Young, Barry Brune, Christiane Müllner, Daniel Loewen, Christopher Alber, Frank Weis, Karsten J Cell Biol Research Articles The organization of the genome is nonrandom and important for correct function. Specifically, the nuclear envelope plays a critical role in gene regulation. It generally constitutes a repressive environment, but several genes, including the GAL locus in budding yeast, are recruited to the nuclear periphery on activation. Here, we combine imaging and computational modeling to ask how the association of a single gene locus with the nuclear envelope influences the surrounding chromosome architecture. Systematic analysis of an entire yeast chromosome establishes that peripheral recruitment of the GAL locus is part of a large-scale rearrangement that shifts many chromosomal regions closer to the nuclear envelope. This process is likely caused by the presence of several independent anchoring points. To identify novel factors required for peripheral anchoring, we performed a genome-wide screen and demonstrated that the histone acetyltransferase SAGA and the activity of histone deacetylases are needed for this extensive gene recruitment to the nuclear periphery. The Rockefeller University Press 2016-02-01 /pmc/articles/PMC4748577/ /pubmed/26811423 http://dx.doi.org/10.1083/jcb.201507069 Text en © 2016 Dultz et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Dultz, Elisa Tjong, Harianto Weider, Elodie Herzog, Mareike Young, Barry Brune, Christiane Müllner, Daniel Loewen, Christopher Alber, Frank Weis, Karsten Global reorganization of budding yeast chromosome conformation in different physiological conditions |
title | Global reorganization of budding yeast chromosome conformation in different physiological conditions |
title_full | Global reorganization of budding yeast chromosome conformation in different physiological conditions |
title_fullStr | Global reorganization of budding yeast chromosome conformation in different physiological conditions |
title_full_unstemmed | Global reorganization of budding yeast chromosome conformation in different physiological conditions |
title_short | Global reorganization of budding yeast chromosome conformation in different physiological conditions |
title_sort | global reorganization of budding yeast chromosome conformation in different physiological conditions |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748577/ https://www.ncbi.nlm.nih.gov/pubmed/26811423 http://dx.doi.org/10.1083/jcb.201507069 |
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