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Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat
BACKGROUND: Global RNA sequencing technologies have revealed widespread RNA polymerase II (Pol II) transcription outside of gene promoters. Small 5′-capped RNA sequencing (Start-seq) originally developed for the detection of promoter-proximal Pol II pausing has helped improve annotation of Transcrip...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558777/ https://www.ncbi.nlm.nih.gov/pubmed/31185909 http://dx.doi.org/10.1186/s12864-019-5829-4 |
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author | Scheidegger, Adam Dunn, Carissa J. Samarakkody, Ann Koney, Nii Koney-Kwaku Perley, Danielle Saha, Ramendra N. Nechaev, Sergei |
author_facet | Scheidegger, Adam Dunn, Carissa J. Samarakkody, Ann Koney, Nii Koney-Kwaku Perley, Danielle Saha, Ramendra N. Nechaev, Sergei |
author_sort | Scheidegger, Adam |
collection | PubMed |
description | BACKGROUND: Global RNA sequencing technologies have revealed widespread RNA polymerase II (Pol II) transcription outside of gene promoters. Small 5′-capped RNA sequencing (Start-seq) originally developed for the detection of promoter-proximal Pol II pausing has helped improve annotation of Transcription Start Sites (TSSs) of genes as well as identification of non-genic regulatory elements. However, apart from the most well studied genomes of human and mouse, mammalian transcription has not been profiled with sufficiently high precision. RESULTS: We prepared and sequenced Start-seq libraries from rat (Rattus norgevicus) primary neural progenitor cells. Over 48 million uniquely mappable reads from two independent biological replicates allowed us to define the TSSs of 7365 known genes in the rn6 genome, reannotating 2503 TSSs by more than 5 base pairs, characterize promoter-associated antisense transcription, and profile Pol II pausing. By combining TSS data with polyA-selected RNA sequencing, we also identified thousands of potential new genes producing stable RNA as well as non-genic transcripts representing possible regulatory elements. CONCLUSIONS: Our study has produced the first Start-seq dataset for the rat. Apart from profiling transcription initiation, our data reaffirm the prevalence of Pol II pausing across the rat genome and indicate conservation of pausing mechanisms across metazoan genomes. We suggest that pausing location, at least in mammals, is constrained by a distance from initiation of transcription, whether it occurs at or outside of a gene promoter. Abundant antisense transcription initiation around protein coding genes indicates that Pol II recruited to the vicinity of a promoter is distributed to available start sites of transcription at either DNA strand. Transcriptome profiling of neural progenitors presented here will facilitate further studies of other rat cell types as well as other organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5829-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6558777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65587772019-06-13 Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat Scheidegger, Adam Dunn, Carissa J. Samarakkody, Ann Koney, Nii Koney-Kwaku Perley, Danielle Saha, Ramendra N. Nechaev, Sergei BMC Genomics Research Article BACKGROUND: Global RNA sequencing technologies have revealed widespread RNA polymerase II (Pol II) transcription outside of gene promoters. Small 5′-capped RNA sequencing (Start-seq) originally developed for the detection of promoter-proximal Pol II pausing has helped improve annotation of Transcription Start Sites (TSSs) of genes as well as identification of non-genic regulatory elements. However, apart from the most well studied genomes of human and mouse, mammalian transcription has not been profiled with sufficiently high precision. RESULTS: We prepared and sequenced Start-seq libraries from rat (Rattus norgevicus) primary neural progenitor cells. Over 48 million uniquely mappable reads from two independent biological replicates allowed us to define the TSSs of 7365 known genes in the rn6 genome, reannotating 2503 TSSs by more than 5 base pairs, characterize promoter-associated antisense transcription, and profile Pol II pausing. By combining TSS data with polyA-selected RNA sequencing, we also identified thousands of potential new genes producing stable RNA as well as non-genic transcripts representing possible regulatory elements. CONCLUSIONS: Our study has produced the first Start-seq dataset for the rat. Apart from profiling transcription initiation, our data reaffirm the prevalence of Pol II pausing across the rat genome and indicate conservation of pausing mechanisms across metazoan genomes. We suggest that pausing location, at least in mammals, is constrained by a distance from initiation of transcription, whether it occurs at or outside of a gene promoter. Abundant antisense transcription initiation around protein coding genes indicates that Pol II recruited to the vicinity of a promoter is distributed to available start sites of transcription at either DNA strand. Transcriptome profiling of neural progenitors presented here will facilitate further studies of other rat cell types as well as other organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5829-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-11 /pmc/articles/PMC6558777/ /pubmed/31185909 http://dx.doi.org/10.1186/s12864-019-5829-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Scheidegger, Adam Dunn, Carissa J. Samarakkody, Ann Koney, Nii Koney-Kwaku Perley, Danielle Saha, Ramendra N. Nechaev, Sergei Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat |
title | Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat |
title_full | Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat |
title_fullStr | Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat |
title_full_unstemmed | Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat |
title_short | Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat |
title_sort | genome-wide rna pol ii initiation and pausing in neural progenitors of the rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558777/ https://www.ncbi.nlm.nih.gov/pubmed/31185909 http://dx.doi.org/10.1186/s12864-019-5829-4 |
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