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Epigenetic memory independent of symmetric histone inheritance
Heterochromatic gene silencing is an important form of gene regulation that usually requires specific histone modifications. A popular model posits that inheritance of modified histones, especially in the form of H3-H4 tetramers, underlies inheritance of heterochromatin. Because H3-H4 tetramers are...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850775/ https://www.ncbi.nlm.nih.gov/pubmed/31613222 http://dx.doi.org/10.7554/eLife.51421 |
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author | Saxton, Daniel S Rine, Jasper |
author_facet | Saxton, Daniel S Rine, Jasper |
author_sort | Saxton, Daniel S |
collection | PubMed |
description | Heterochromatic gene silencing is an important form of gene regulation that usually requires specific histone modifications. A popular model posits that inheritance of modified histones, especially in the form of H3-H4 tetramers, underlies inheritance of heterochromatin. Because H3-H4 tetramers are randomly distributed between daughter chromatids during DNA replication, rare occurrences of asymmetric tetramer inheritance within a heterochromatic domain would have the potential to destabilize heterochromatin. This model makes a prediction that shorter heterochromatic domains would experience unbalanced tetramer inheritance more frequently, and thereby be less stable. In contrast to this prediction, we found that shortening a heterochromatic domain in Saccharomyces had no impact on the strength of silencing nor its heritability. Additionally, we found that replisome mutations that disrupt inheritance of H3-H4 tetramers had only minor effects on heterochromatin stability. These findings suggest that histones carry little or no memory of the heterochromatin state through DNA replication. |
format | Online Article Text |
id | pubmed-6850775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68507752019-11-14 Epigenetic memory independent of symmetric histone inheritance Saxton, Daniel S Rine, Jasper eLife Chromosomes and Gene Expression Heterochromatic gene silencing is an important form of gene regulation that usually requires specific histone modifications. A popular model posits that inheritance of modified histones, especially in the form of H3-H4 tetramers, underlies inheritance of heterochromatin. Because H3-H4 tetramers are randomly distributed between daughter chromatids during DNA replication, rare occurrences of asymmetric tetramer inheritance within a heterochromatic domain would have the potential to destabilize heterochromatin. This model makes a prediction that shorter heterochromatic domains would experience unbalanced tetramer inheritance more frequently, and thereby be less stable. In contrast to this prediction, we found that shortening a heterochromatic domain in Saccharomyces had no impact on the strength of silencing nor its heritability. Additionally, we found that replisome mutations that disrupt inheritance of H3-H4 tetramers had only minor effects on heterochromatin stability. These findings suggest that histones carry little or no memory of the heterochromatin state through DNA replication. eLife Sciences Publications, Ltd 2019-10-15 /pmc/articles/PMC6850775/ /pubmed/31613222 http://dx.doi.org/10.7554/eLife.51421 Text en © 2019, Saxton and Rine http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Chromosomes and Gene Expression Saxton, Daniel S Rine, Jasper Epigenetic memory independent of symmetric histone inheritance |
title | Epigenetic memory independent of symmetric histone inheritance |
title_full | Epigenetic memory independent of symmetric histone inheritance |
title_fullStr | Epigenetic memory independent of symmetric histone inheritance |
title_full_unstemmed | Epigenetic memory independent of symmetric histone inheritance |
title_short | Epigenetic memory independent of symmetric histone inheritance |
title_sort | epigenetic memory independent of symmetric histone inheritance |
topic | Chromosomes and Gene Expression |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850775/ https://www.ncbi.nlm.nih.gov/pubmed/31613222 http://dx.doi.org/10.7554/eLife.51421 |
work_keys_str_mv | AT saxtondaniels epigeneticmemoryindependentofsymmetrichistoneinheritance AT rinejasper epigeneticmemoryindependentofsymmetrichistoneinheritance |