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Timing RNA polymerase pausing with TV-PRO-seq

Transcription of many genes in metazoans is subject to polymerase pausing, which is the transient stop of transcriptionally engaged polymerases. This is known to mainly occur in promoter-proximal regions but it is not well understood. In particular, a genome-wide measurement of pausing times at high...

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Autores principales: Zhang, Jie, Cavallaro, Massimo, Hebenstreit, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547241/
https://www.ncbi.nlm.nih.gov/pubmed/34723238
http://dx.doi.org/10.1016/j.crmeth.2021.100083
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author Zhang, Jie
Cavallaro, Massimo
Hebenstreit, Daniel
author_facet Zhang, Jie
Cavallaro, Massimo
Hebenstreit, Daniel
author_sort Zhang, Jie
collection PubMed
description Transcription of many genes in metazoans is subject to polymerase pausing, which is the transient stop of transcriptionally engaged polymerases. This is known to mainly occur in promoter-proximal regions but it is not well understood. In particular, a genome-wide measurement of pausing times at high resolution has been lacking. We present here the time-variant precision nuclear run-on and sequencing (TV-PRO-seq) assay, an extension of the standard PRO-seq that allows us to estimate genome-wide pausing times at single-base resolution. Its application to human cells demonstrates that, proximal to promoters, polymerases pause more frequently but for shorter times than in other genomic regions. Comparison with single-cell gene expression data reveals that the polymerase pausing times are longer in highly expressed genes, while transcriptionally noisier genes have higher pausing frequencies and slightly longer pausing times. Analyses of histone modifications suggest that the marker H3K36me3 is related to the polymerase pausing.
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spelling pubmed-85472412021-10-29 Timing RNA polymerase pausing with TV-PRO-seq Zhang, Jie Cavallaro, Massimo Hebenstreit, Daniel Cell Rep Methods Article Transcription of many genes in metazoans is subject to polymerase pausing, which is the transient stop of transcriptionally engaged polymerases. This is known to mainly occur in promoter-proximal regions but it is not well understood. In particular, a genome-wide measurement of pausing times at high resolution has been lacking. We present here the time-variant precision nuclear run-on and sequencing (TV-PRO-seq) assay, an extension of the standard PRO-seq that allows us to estimate genome-wide pausing times at single-base resolution. Its application to human cells demonstrates that, proximal to promoters, polymerases pause more frequently but for shorter times than in other genomic regions. Comparison with single-cell gene expression data reveals that the polymerase pausing times are longer in highly expressed genes, while transcriptionally noisier genes have higher pausing frequencies and slightly longer pausing times. Analyses of histone modifications suggest that the marker H3K36me3 is related to the polymerase pausing. Elsevier 2021-09-27 /pmc/articles/PMC8547241/ /pubmed/34723238 http://dx.doi.org/10.1016/j.crmeth.2021.100083 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Zhang, Jie
Cavallaro, Massimo
Hebenstreit, Daniel
Timing RNA polymerase pausing with TV-PRO-seq
title Timing RNA polymerase pausing with TV-PRO-seq
title_full Timing RNA polymerase pausing with TV-PRO-seq
title_fullStr Timing RNA polymerase pausing with TV-PRO-seq
title_full_unstemmed Timing RNA polymerase pausing with TV-PRO-seq
title_short Timing RNA polymerase pausing with TV-PRO-seq
title_sort timing rna polymerase pausing with tv-pro-seq
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547241/
https://www.ncbi.nlm.nih.gov/pubmed/34723238
http://dx.doi.org/10.1016/j.crmeth.2021.100083
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