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RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development
According to previous studies, during Drosophila embryogenesis, the recruitment of RNA polymerase II precedes active gene transcription. This work is aimed at exploring whether this mechanism is used during Drosophila metamorphosis. In addition, the composition of the RNA polymerase II “paused” comp...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503990/ https://www.ncbi.nlm.nih.gov/pubmed/36142573 http://dx.doi.org/10.3390/ijms231810662 |
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author | Mazina, Marina Yu. Kovalenko, Elena V. Evdokimova, Aleksandra A. Erokhin, Maksim Chetverina, Darya Vorobyeva, Nadezhda E. |
author_facet | Mazina, Marina Yu. Kovalenko, Elena V. Evdokimova, Aleksandra A. Erokhin, Maksim Chetverina, Darya Vorobyeva, Nadezhda E. |
author_sort | Mazina, Marina Yu. |
collection | PubMed |
description | According to previous studies, during Drosophila embryogenesis, the recruitment of RNA polymerase II precedes active gene transcription. This work is aimed at exploring whether this mechanism is used during Drosophila metamorphosis. In addition, the composition of the RNA polymerase II “paused” complexes associated with promoters at different developmental stages are described in detail. For this purpose, we performed ChIP-Seq analysis using antibodies for various modifications of RNA polymerase II (total, Pol II CTD Ser5P, and Pol II CTD Ser2P) as well as for subunits of the NELF, DSIF, and PAF complexes and Brd4/Fs(1)h that control transcription elongation. We found that during metamorphosis, similar to mid-embryogenesis, the promoters were bound by RNA polymerase II in the “paused” state, preparing for activation at later stages of development. During mid-embryogenesis, RNA polymerase II in a “pause” state was phosphorylated at Ser5 and Ser2 of Pol II CTD and bound the NELF, DSIF, and PAF complexes, but not Brd4/Fs(1)h. During metamorphosis, the “paused” RNA polymerase II complex included Brd4/Fs(1)h in addition to NELF, DSIF, and PAF. The RNA polymerase II in this complex was phosphorylated at Ser5 of Pol II CTD, but not at Ser2. These results indicate that, during mid-embryogenesis, RNA polymerase II stalls in the “post-pause” state, being phosphorylated at Ser2 of Pol II CTD (after the stage of p-TEFb action). During metamorphosis, the “pause” mechanism is closer to classical promoter-proximal pausing and is characterized by a low level of Pol II CTD Ser2P. |
format | Online Article Text |
id | pubmed-9503990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95039902022-09-24 RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development Mazina, Marina Yu. Kovalenko, Elena V. Evdokimova, Aleksandra A. Erokhin, Maksim Chetverina, Darya Vorobyeva, Nadezhda E. Int J Mol Sci Article According to previous studies, during Drosophila embryogenesis, the recruitment of RNA polymerase II precedes active gene transcription. This work is aimed at exploring whether this mechanism is used during Drosophila metamorphosis. In addition, the composition of the RNA polymerase II “paused” complexes associated with promoters at different developmental stages are described in detail. For this purpose, we performed ChIP-Seq analysis using antibodies for various modifications of RNA polymerase II (total, Pol II CTD Ser5P, and Pol II CTD Ser2P) as well as for subunits of the NELF, DSIF, and PAF complexes and Brd4/Fs(1)h that control transcription elongation. We found that during metamorphosis, similar to mid-embryogenesis, the promoters were bound by RNA polymerase II in the “paused” state, preparing for activation at later stages of development. During mid-embryogenesis, RNA polymerase II in a “pause” state was phosphorylated at Ser5 and Ser2 of Pol II CTD and bound the NELF, DSIF, and PAF complexes, but not Brd4/Fs(1)h. During metamorphosis, the “paused” RNA polymerase II complex included Brd4/Fs(1)h in addition to NELF, DSIF, and PAF. The RNA polymerase II in this complex was phosphorylated at Ser5 of Pol II CTD, but not at Ser2. These results indicate that, during mid-embryogenesis, RNA polymerase II stalls in the “post-pause” state, being phosphorylated at Ser2 of Pol II CTD (after the stage of p-TEFb action). During metamorphosis, the “pause” mechanism is closer to classical promoter-proximal pausing and is characterized by a low level of Pol II CTD Ser2P. MDPI 2022-09-13 /pmc/articles/PMC9503990/ /pubmed/36142573 http://dx.doi.org/10.3390/ijms231810662 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mazina, Marina Yu. Kovalenko, Elena V. Evdokimova, Aleksandra A. Erokhin, Maksim Chetverina, Darya Vorobyeva, Nadezhda E. RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development |
title | RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development |
title_full | RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development |
title_fullStr | RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development |
title_full_unstemmed | RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development |
title_short | RNA Polymerase II “Pause” Prepares Promoters for Upcoming Transcription during Drosophila Development |
title_sort | rna polymerase ii “pause” prepares promoters for upcoming transcription during drosophila development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503990/ https://www.ncbi.nlm.nih.gov/pubmed/36142573 http://dx.doi.org/10.3390/ijms231810662 |
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