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ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling
Chromatin assembly involves the combined action of ATP-dependent motor proteins and histone chaperones. Because motor proteins in chromatin assembly also function as chromatin remodeling factors, we investigated the relationship between ATP-driven chromatin assembly and chromatin remodeling in the g...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748710/ https://www.ncbi.nlm.nih.gov/pubmed/23986862 http://dx.doi.org/10.7554/eLife.00863 |
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author | Torigoe, Sharon E Patel, Ashok Khuong, Mai T Bowman, Gregory D Kadonaga, James T |
author_facet | Torigoe, Sharon E Patel, Ashok Khuong, Mai T Bowman, Gregory D Kadonaga, James T |
author_sort | Torigoe, Sharon E |
collection | PubMed |
description | Chromatin assembly involves the combined action of ATP-dependent motor proteins and histone chaperones. Because motor proteins in chromatin assembly also function as chromatin remodeling factors, we investigated the relationship between ATP-driven chromatin assembly and chromatin remodeling in the generation of periodic nucleosome arrays. We found that chromatin remodeling-defective Chd1 motor proteins are able to catalyze ATP-dependent chromatin assembly. The resulting nucleosomes are not, however, spaced in periodic arrays. Wild-type Chd1, but not chromatin remodeling-defective Chd1, can catalyze the conversion of randomly-distributed nucleosomes into periodic arrays. These results reveal a functional distinction between ATP-dependent nucleosome assembly and chromatin remodeling, and suggest a model for chromatin assembly in which randomly-distributed nucleosomes are formed by the nucleosome assembly function of Chd1, and then regularly-spaced nucleosome arrays are generated by the chromatin remodeling activity of Chd1. These findings uncover an unforeseen level of specificity in the role of motor proteins in chromatin assembly. DOI: http://dx.doi.org/10.7554/eLife.00863.001 |
format | Online Article Text |
id | pubmed-3748710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37487102013-08-28 ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling Torigoe, Sharon E Patel, Ashok Khuong, Mai T Bowman, Gregory D Kadonaga, James T eLife Biochemistry Chromatin assembly involves the combined action of ATP-dependent motor proteins and histone chaperones. Because motor proteins in chromatin assembly also function as chromatin remodeling factors, we investigated the relationship between ATP-driven chromatin assembly and chromatin remodeling in the generation of periodic nucleosome arrays. We found that chromatin remodeling-defective Chd1 motor proteins are able to catalyze ATP-dependent chromatin assembly. The resulting nucleosomes are not, however, spaced in periodic arrays. Wild-type Chd1, but not chromatin remodeling-defective Chd1, can catalyze the conversion of randomly-distributed nucleosomes into periodic arrays. These results reveal a functional distinction between ATP-dependent nucleosome assembly and chromatin remodeling, and suggest a model for chromatin assembly in which randomly-distributed nucleosomes are formed by the nucleosome assembly function of Chd1, and then regularly-spaced nucleosome arrays are generated by the chromatin remodeling activity of Chd1. These findings uncover an unforeseen level of specificity in the role of motor proteins in chromatin assembly. DOI: http://dx.doi.org/10.7554/eLife.00863.001 eLife Sciences Publications, Ltd 2013-08-20 /pmc/articles/PMC3748710/ /pubmed/23986862 http://dx.doi.org/10.7554/eLife.00863 Text en Copyright © 2013, Torigoe et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Torigoe, Sharon E Patel, Ashok Khuong, Mai T Bowman, Gregory D Kadonaga, James T ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling |
title | ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling |
title_full | ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling |
title_fullStr | ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling |
title_full_unstemmed | ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling |
title_short | ATP-dependent chromatin assembly is functionally distinct from chromatin remodeling |
title_sort | atp-dependent chromatin assembly is functionally distinct from chromatin remodeling |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748710/ https://www.ncbi.nlm.nih.gov/pubmed/23986862 http://dx.doi.org/10.7554/eLife.00863 |
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