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Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration
The interplay between nucleosomes and transcription factors leads to programs of gene expression. Transcriptional silencing involves the generation of a chromatin state that represses transcription and is faithfully propagated through DNA replication and cell division. Using multiple reporter assays...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592971/ https://www.ncbi.nlm.nih.gov/pubmed/37873261 http://dx.doi.org/10.1101/2023.10.05.561072 |
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author | Wu, Kenneth Dhillon, Namrita Bajor, Antone Abrahamson, Sara Kamakaka, Rohinton T. |
author_facet | Wu, Kenneth Dhillon, Namrita Bajor, Antone Abrahamson, Sara Kamakaka, Rohinton T. |
author_sort | Wu, Kenneth |
collection | PubMed |
description | The interplay between nucleosomes and transcription factors leads to programs of gene expression. Transcriptional silencing involves the generation of a chromatin state that represses transcription and is faithfully propagated through DNA replication and cell division. Using multiple reporter assays, including directly visualizing transcription in single cells, we investigated a diverse set of UAS enhancers and core promoters for their susceptibility to heterochromatic gene silencing. These results show that heterochromatin only stably silences weak and stress induced regulatory elements but is unable to stably repress housekeeping gene regulatory elements and the partial repression did not result in bistable expression states. Permutation analysis of different UAS enhancers and core promoters indicate that both elements function together to determine the susceptibility of regulatory sequences to repression. Specific histone modifiers and chromatin remodellers function in an enhancer specific manner to aid these elements to resist repression suggesting that Sir proteins likely function in part by reducing nucleosome mobility. We also show that the strong housekeeping regulatory elements can be repressed if silencer bound Sir1 is increased, suggesting that Sir1 is a limiting component in silencing. Together, our data suggest that the heterochromatic locus has been optimized to stably silence the weak mating type gene regulatory elements but not strong housekeeping gene regulatory sequences which could help explain why these genes are often found at the boundaries of silenced domains. |
format | Online Article Text |
id | pubmed-10592971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105929712023-10-24 Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration Wu, Kenneth Dhillon, Namrita Bajor, Antone Abrahamson, Sara Kamakaka, Rohinton T. bioRxiv Article The interplay between nucleosomes and transcription factors leads to programs of gene expression. Transcriptional silencing involves the generation of a chromatin state that represses transcription and is faithfully propagated through DNA replication and cell division. Using multiple reporter assays, including directly visualizing transcription in single cells, we investigated a diverse set of UAS enhancers and core promoters for their susceptibility to heterochromatic gene silencing. These results show that heterochromatin only stably silences weak and stress induced regulatory elements but is unable to stably repress housekeeping gene regulatory elements and the partial repression did not result in bistable expression states. Permutation analysis of different UAS enhancers and core promoters indicate that both elements function together to determine the susceptibility of regulatory sequences to repression. Specific histone modifiers and chromatin remodellers function in an enhancer specific manner to aid these elements to resist repression suggesting that Sir proteins likely function in part by reducing nucleosome mobility. We also show that the strong housekeeping regulatory elements can be repressed if silencer bound Sir1 is increased, suggesting that Sir1 is a limiting component in silencing. Together, our data suggest that the heterochromatic locus has been optimized to stably silence the weak mating type gene regulatory elements but not strong housekeeping gene regulatory sequences which could help explain why these genes are often found at the boundaries of silenced domains. Cold Spring Harbor Laboratory 2023-10-05 /pmc/articles/PMC10592971/ /pubmed/37873261 http://dx.doi.org/10.1101/2023.10.05.561072 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Wu, Kenneth Dhillon, Namrita Bajor, Antone Abrahamson, Sara Kamakaka, Rohinton T. Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration |
title | Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration |
title_full | Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration |
title_fullStr | Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration |
title_full_unstemmed | Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration |
title_short | Yeast Heterochromatin Only Stably Silences Weak Regulatory Elements by Altering Burst Duration |
title_sort | yeast heterochromatin only stably silences weak regulatory elements by altering burst duration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592971/ https://www.ncbi.nlm.nih.gov/pubmed/37873261 http://dx.doi.org/10.1101/2023.10.05.561072 |
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