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Organismal benefits of transcription speed control at gene boundaries
RNA polymerase II (RNAPII) transcription is crucial for gene expression. RNAPII density peaks at gene boundaries, associating these key regions for gene expression control with limited RNAPII movement. The connections between RNAPII transcription speed and gene regulation in multicellular organisms...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132196/ https://www.ncbi.nlm.nih.gov/pubmed/32103605 http://dx.doi.org/10.15252/embr.201949315 |
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author | Leng, Xueyuan Ivanov, Maxim Kindgren, Peter Malik, Indranil Thieffry, Axel Brodersen, Peter Sandelin, Albin Kaplan, Craig D Marquardt, Sebastian |
author_facet | Leng, Xueyuan Ivanov, Maxim Kindgren, Peter Malik, Indranil Thieffry, Axel Brodersen, Peter Sandelin, Albin Kaplan, Craig D Marquardt, Sebastian |
author_sort | Leng, Xueyuan |
collection | PubMed |
description | RNA polymerase II (RNAPII) transcription is crucial for gene expression. RNAPII density peaks at gene boundaries, associating these key regions for gene expression control with limited RNAPII movement. The connections between RNAPII transcription speed and gene regulation in multicellular organisms are poorly understood. Here, we directly modulate RNAPII transcription speed by point mutations in the second largest subunit of RNAPII in Arabidopsis thaliana. A RNAPII mutation predicted to decelerate transcription is inviable, while accelerating RNAPII transcription confers phenotypes resembling auto‐immunity. Nascent transcription profiling revealed that RNAPII complexes with accelerated transcription clear stalling sites at both gene ends, resulting in read‐through transcription. The accelerated transcription mutant NRPB2‐Y732F exhibits increased association with 5′ splice site (5′SS) intermediates and enhanced splicing efficiency. Our findings highlight potential advantages of RNAPII stalling through local reduction in transcription speed to optimize gene expression for the development of multicellular organisms. |
format | Online Article Text |
id | pubmed-7132196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71321962020-04-06 Organismal benefits of transcription speed control at gene boundaries Leng, Xueyuan Ivanov, Maxim Kindgren, Peter Malik, Indranil Thieffry, Axel Brodersen, Peter Sandelin, Albin Kaplan, Craig D Marquardt, Sebastian EMBO Rep Articles RNA polymerase II (RNAPII) transcription is crucial for gene expression. RNAPII density peaks at gene boundaries, associating these key regions for gene expression control with limited RNAPII movement. The connections between RNAPII transcription speed and gene regulation in multicellular organisms are poorly understood. Here, we directly modulate RNAPII transcription speed by point mutations in the second largest subunit of RNAPII in Arabidopsis thaliana. A RNAPII mutation predicted to decelerate transcription is inviable, while accelerating RNAPII transcription confers phenotypes resembling auto‐immunity. Nascent transcription profiling revealed that RNAPII complexes with accelerated transcription clear stalling sites at both gene ends, resulting in read‐through transcription. The accelerated transcription mutant NRPB2‐Y732F exhibits increased association with 5′ splice site (5′SS) intermediates and enhanced splicing efficiency. Our findings highlight potential advantages of RNAPII stalling through local reduction in transcription speed to optimize gene expression for the development of multicellular organisms. John Wiley and Sons Inc. 2020-02-27 2020-04-03 /pmc/articles/PMC7132196/ /pubmed/32103605 http://dx.doi.org/10.15252/embr.201949315 Text en © 2020 The Authors. Published under the terms of the CC BY NC ND 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Leng, Xueyuan Ivanov, Maxim Kindgren, Peter Malik, Indranil Thieffry, Axel Brodersen, Peter Sandelin, Albin Kaplan, Craig D Marquardt, Sebastian Organismal benefits of transcription speed control at gene boundaries |
title | Organismal benefits of transcription speed control at gene boundaries |
title_full | Organismal benefits of transcription speed control at gene boundaries |
title_fullStr | Organismal benefits of transcription speed control at gene boundaries |
title_full_unstemmed | Organismal benefits of transcription speed control at gene boundaries |
title_short | Organismal benefits of transcription speed control at gene boundaries |
title_sort | organismal benefits of transcription speed control at gene boundaries |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132196/ https://www.ncbi.nlm.nih.gov/pubmed/32103605 http://dx.doi.org/10.15252/embr.201949315 |
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