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Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions
BACKGROUND: In contrast to unidirectional promoters wherein antisense transcription results in short transcripts which are rapidly degraded, bidirectional promoters produce mature transcripts in both sense and antisense orientation. To understand the molecular mechanism of how productive bidirection...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930751/ https://www.ncbi.nlm.nih.gov/pubmed/29716520 http://dx.doi.org/10.1186/s12864-018-4697-7 |
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author | Jangid, Rahul Kumar Kelkar, Ashwin Muley, Vijaykumar Yogesh Galande, Sanjeev |
author_facet | Jangid, Rahul Kumar Kelkar, Ashwin Muley, Vijaykumar Yogesh Galande, Sanjeev |
author_sort | Jangid, Rahul Kumar |
collection | PubMed |
description | BACKGROUND: In contrast to unidirectional promoters wherein antisense transcription results in short transcripts which are rapidly degraded, bidirectional promoters produce mature transcripts in both sense and antisense orientation. To understand the molecular mechanism of how productive bidirectional transcription is regulated, we focused on delineating the chromatin signature of bidirectional promoters. RESULTS: We report generation and utility of a reporter system that enables simultaneous scoring of transcriptional activity in opposite directions. Testing of putative bidirectional promoters in this system demonstrates no measurable bias towards any one direction of transcription. We analyzed the NUP26L-PIH1D3 bidirectional gene pair during Retinoic acid mediated differentiation of embryonic carcinoma cells. In their native context, we observed that the chromatin landscape at and around the transcription regulatory region between the pair of bidirectional genes is modulated in concordance with transcriptional activity of each gene in the pair. We then extended this analysis to 974 bidirectional gene pairs in two different cell lines, H1 human embryonic stem cells and CD4 positive T cells using publicly available ChIP-Seq and RNA-Seq data. Bidirectional gene pairs were classified based on the intergenic distance separating the two TSS of the transcripts analyzed as well as the relative expression of each transcript in a bidirectional gene pair. We report that for the entire range of intergenic distance separating bidirectional genes, the expression profile of such genes (symmetric or asymmetric) matches the histone modification profile of marks associated with active transcription initiation and elongation. CONCLUSIONS: We demonstrate unique distribution of histone modification marks that correlate robustly with the transcription status of genes regulated by bidirectional promoters. These findings strongly imply that occurrence of these marks might signal the transcription machinery to drive maturation of antisense transcription from the bidirectional promoters. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4697-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5930751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59307512018-05-09 Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions Jangid, Rahul Kumar Kelkar, Ashwin Muley, Vijaykumar Yogesh Galande, Sanjeev BMC Genomics Research Article BACKGROUND: In contrast to unidirectional promoters wherein antisense transcription results in short transcripts which are rapidly degraded, bidirectional promoters produce mature transcripts in both sense and antisense orientation. To understand the molecular mechanism of how productive bidirectional transcription is regulated, we focused on delineating the chromatin signature of bidirectional promoters. RESULTS: We report generation and utility of a reporter system that enables simultaneous scoring of transcriptional activity in opposite directions. Testing of putative bidirectional promoters in this system demonstrates no measurable bias towards any one direction of transcription. We analyzed the NUP26L-PIH1D3 bidirectional gene pair during Retinoic acid mediated differentiation of embryonic carcinoma cells. In their native context, we observed that the chromatin landscape at and around the transcription regulatory region between the pair of bidirectional genes is modulated in concordance with transcriptional activity of each gene in the pair. We then extended this analysis to 974 bidirectional gene pairs in two different cell lines, H1 human embryonic stem cells and CD4 positive T cells using publicly available ChIP-Seq and RNA-Seq data. Bidirectional gene pairs were classified based on the intergenic distance separating the two TSS of the transcripts analyzed as well as the relative expression of each transcript in a bidirectional gene pair. We report that for the entire range of intergenic distance separating bidirectional genes, the expression profile of such genes (symmetric or asymmetric) matches the histone modification profile of marks associated with active transcription initiation and elongation. CONCLUSIONS: We demonstrate unique distribution of histone modification marks that correlate robustly with the transcription status of genes regulated by bidirectional promoters. These findings strongly imply that occurrence of these marks might signal the transcription machinery to drive maturation of antisense transcription from the bidirectional promoters. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4697-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-02 /pmc/articles/PMC5930751/ /pubmed/29716520 http://dx.doi.org/10.1186/s12864-018-4697-7 Text en © The Author(s). 2018 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 Jangid, Rahul Kumar Kelkar, Ashwin Muley, Vijaykumar Yogesh Galande, Sanjeev Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions |
title | Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions |
title_full | Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions |
title_fullStr | Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions |
title_full_unstemmed | Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions |
title_short | Bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions |
title_sort | bidirectional promoters exhibit characteristic chromatin modification signature associated with transcription elongation in both sense and antisense directions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930751/ https://www.ncbi.nlm.nih.gov/pubmed/29716520 http://dx.doi.org/10.1186/s12864-018-4697-7 |
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