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Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters

During RNA polymerase II (RNA Pol II) transcription, the chromatin structure undergoes dynamic changes, including opening and closing of the nucleosome to enhance transcription elongation and fidelity. These changes are mediated by transcription elongation factors, including Spt6, the FACT complex,...

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Autores principales: Lee, Bo Bae, Woo, Hyeonju, Lee, Min Kyung, Youn, SeoJung, Lee, Sumin, Roe, Jae-Seok, Lee, Soo Young, Kim, TaeSoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373055/
https://www.ncbi.nlm.nih.gov/pubmed/34320189
http://dx.doi.org/10.1093/nar/gkab639
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author Lee, Bo Bae
Woo, Hyeonju
Lee, Min Kyung
Youn, SeoJung
Lee, Sumin
Roe, Jae-Seok
Lee, Soo Young
Kim, TaeSoo
author_facet Lee, Bo Bae
Woo, Hyeonju
Lee, Min Kyung
Youn, SeoJung
Lee, Sumin
Roe, Jae-Seok
Lee, Soo Young
Kim, TaeSoo
author_sort Lee, Bo Bae
collection PubMed
description During RNA polymerase II (RNA Pol II) transcription, the chromatin structure undergoes dynamic changes, including opening and closing of the nucleosome to enhance transcription elongation and fidelity. These changes are mediated by transcription elongation factors, including Spt6, the FACT complex, and the Set2-Rpd3S HDAC pathway. These factors not only contribute to RNA Pol II elongation, reset the repressive chromatin structures after RNA Pol II has passed, thereby inhibiting aberrant transcription initiation from the internal cryptic promoters within gene bodies. Notably, the internal cryptic promoters of infrequently transcribed genes are sensitive to such chromatin-based regulation but those of hyperactive genes are not. To determine why, the weak core promoters of genes that generate cryptic transcripts in cells lacking transcription elongation factors (e.g. STE11) were replaced with those from more active genes. Interestingly, as core promoter activity increased, activation of internal cryptic promoter dropped. This associated with loss of active histone modifications at the internal cryptic promoter. Moreover, environmental changes and transcription elongation factor mutations that downregulated the core promoters of highly active genes concomitantly increased their cryptic transcription. We therefore propose that the chromatin-based regulation of internal cryptic promoters is mediated by core promoter strength as well as transcription elongation factors.
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spelling pubmed-83730552021-08-19 Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters Lee, Bo Bae Woo, Hyeonju Lee, Min Kyung Youn, SeoJung Lee, Sumin Roe, Jae-Seok Lee, Soo Young Kim, TaeSoo Nucleic Acids Res Gene regulation, Chromatin and Epigenetics During RNA polymerase II (RNA Pol II) transcription, the chromatin structure undergoes dynamic changes, including opening and closing of the nucleosome to enhance transcription elongation and fidelity. These changes are mediated by transcription elongation factors, including Spt6, the FACT complex, and the Set2-Rpd3S HDAC pathway. These factors not only contribute to RNA Pol II elongation, reset the repressive chromatin structures after RNA Pol II has passed, thereby inhibiting aberrant transcription initiation from the internal cryptic promoters within gene bodies. Notably, the internal cryptic promoters of infrequently transcribed genes are sensitive to such chromatin-based regulation but those of hyperactive genes are not. To determine why, the weak core promoters of genes that generate cryptic transcripts in cells lacking transcription elongation factors (e.g. STE11) were replaced with those from more active genes. Interestingly, as core promoter activity increased, activation of internal cryptic promoter dropped. This associated with loss of active histone modifications at the internal cryptic promoter. Moreover, environmental changes and transcription elongation factor mutations that downregulated the core promoters of highly active genes concomitantly increased their cryptic transcription. We therefore propose that the chromatin-based regulation of internal cryptic promoters is mediated by core promoter strength as well as transcription elongation factors. Oxford University Press 2021-07-28 /pmc/articles/PMC8373055/ /pubmed/34320189 http://dx.doi.org/10.1093/nar/gkab639 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Lee, Bo Bae
Woo, Hyeonju
Lee, Min Kyung
Youn, SeoJung
Lee, Sumin
Roe, Jae-Seok
Lee, Soo Young
Kim, TaeSoo
Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters
title Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters
title_full Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters
title_fullStr Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters
title_full_unstemmed Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters
title_short Core promoter activity contributes to chromatin-based regulation of internal cryptic promoters
title_sort core promoter activity contributes to chromatin-based regulation of internal cryptic promoters
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373055/
https://www.ncbi.nlm.nih.gov/pubmed/34320189
http://dx.doi.org/10.1093/nar/gkab639
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