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Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue
The dynamics of the RNA polymerase II (Pol II) backtracking process is poorly understood. We built a Markov State Model from extensive molecular dynamics simulations to identify metastable intermediate states and the dynamics of backtracking at atomistic detail. Our results reveal that Pol II backtr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838855/ https://www.ncbi.nlm.nih.gov/pubmed/27091704 http://dx.doi.org/10.1038/ncomms11244 |
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author | Da, Lin-Tai Pardo-Avila, Fátima Xu, Liang Silva, Daniel-Adriano Zhang, Lu Gao, Xin Wang, Dong Huang, Xuhui |
author_facet | Da, Lin-Tai Pardo-Avila, Fátima Xu, Liang Silva, Daniel-Adriano Zhang, Lu Gao, Xin Wang, Dong Huang, Xuhui |
author_sort | Da, Lin-Tai |
collection | PubMed |
description | The dynamics of the RNA polymerase II (Pol II) backtracking process is poorly understood. We built a Markov State Model from extensive molecular dynamics simulations to identify metastable intermediate states and the dynamics of backtracking at atomistic detail. Our results reveal that Pol II backtracking occurs in a stepwise mode where two intermediate states are involved. We find that the continuous bending motion of the Bridge helix (BH) serves as a critical checkpoint, using the highly conserved BH residue T831 as a sensing probe for the 3′-terminal base paring of RNA:DNA hybrid. If the base pair is mismatched, BH bending can promote the RNA 3′-end nucleotide into a frayed state that further leads to the backtracked state. These computational observations are validated by site-directed mutagenesis and transcript cleavage assays, and provide insights into the key factors that regulate the preferences of the backward translocation. |
format | Online Article Text |
id | pubmed-4838855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48388552016-05-04 Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue Da, Lin-Tai Pardo-Avila, Fátima Xu, Liang Silva, Daniel-Adriano Zhang, Lu Gao, Xin Wang, Dong Huang, Xuhui Nat Commun Article The dynamics of the RNA polymerase II (Pol II) backtracking process is poorly understood. We built a Markov State Model from extensive molecular dynamics simulations to identify metastable intermediate states and the dynamics of backtracking at atomistic detail. Our results reveal that Pol II backtracking occurs in a stepwise mode where two intermediate states are involved. We find that the continuous bending motion of the Bridge helix (BH) serves as a critical checkpoint, using the highly conserved BH residue T831 as a sensing probe for the 3′-terminal base paring of RNA:DNA hybrid. If the base pair is mismatched, BH bending can promote the RNA 3′-end nucleotide into a frayed state that further leads to the backtracked state. These computational observations are validated by site-directed mutagenesis and transcript cleavage assays, and provide insights into the key factors that regulate the preferences of the backward translocation. Nature Publishing Group 2016-04-19 /pmc/articles/PMC4838855/ /pubmed/27091704 http://dx.doi.org/10.1038/ncomms11244 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Da, Lin-Tai Pardo-Avila, Fátima Xu, Liang Silva, Daniel-Adriano Zhang, Lu Gao, Xin Wang, Dong Huang, Xuhui Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue |
title | Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue |
title_full | Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue |
title_fullStr | Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue |
title_full_unstemmed | Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue |
title_short | Bridge helix bending promotes RNA polymerase II backtracking through a critical and conserved threonine residue |
title_sort | bridge helix bending promotes rna polymerase ii backtracking through a critical and conserved threonine residue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838855/ https://www.ncbi.nlm.nih.gov/pubmed/27091704 http://dx.doi.org/10.1038/ncomms11244 |
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