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MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region

MYB transcriptional elongation is regulated by an attenuator sequence within intron 1 that has been proposed to encode a RNA stem loop (SLR) followed by a polyU tract. We report that NFκBp50 can bind the SLR polyU RNA and promote MYB transcriptional elongation together with NFκBp65. We identified a...

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Autores principales: Pereira, Lloyd A., Hugo, Honor J., Malaterre, Jordane, Huiling, Xu, Sonza, Secondo, Cures, Alina, Purcell, Damian F. J., Ramsland, Paul A., Gerondakis, Steven, Gonda, Thomas J., Ramsay, Robert G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390348/
https://www.ncbi.nlm.nih.gov/pubmed/25853889
http://dx.doi.org/10.1371/journal.pone.0122919
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author Pereira, Lloyd A.
Hugo, Honor J.
Malaterre, Jordane
Huiling, Xu
Sonza, Secondo
Cures, Alina
Purcell, Damian F. J.
Ramsland, Paul A.
Gerondakis, Steven
Gonda, Thomas J.
Ramsay, Robert G.
author_facet Pereira, Lloyd A.
Hugo, Honor J.
Malaterre, Jordane
Huiling, Xu
Sonza, Secondo
Cures, Alina
Purcell, Damian F. J.
Ramsland, Paul A.
Gerondakis, Steven
Gonda, Thomas J.
Ramsay, Robert G.
author_sort Pereira, Lloyd A.
collection PubMed
description MYB transcriptional elongation is regulated by an attenuator sequence within intron 1 that has been proposed to encode a RNA stem loop (SLR) followed by a polyU tract. We report that NFκBp50 can bind the SLR polyU RNA and promote MYB transcriptional elongation together with NFκBp65. We identified a conserved lysine-rich motif within the Rel homology domain (RHD) of NFκBp50, mutation of which abrogated the interaction of NFκBp50 with the SLR polyU and impaired NFκBp50 mediated MYB elongation. We observed that the TAR RNA-binding region of Tat is homologous to the NFκBp50 RHD lysine-rich motif, a finding consistent with HIV Tat acting as an effector of MYB transcriptional elongation in an SLR dependent manner. Furthermore, we identify the DNA binding activity of NFκBp50 as a key component required for the SLR polyU mediated regulation of MYB. Collectively these results suggest that the MYB SLR polyU provides a platform for proteins to regulate MYB and reveals novel nucleic acid binding properties of NFκBp50 required for MYB regulation.
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spelling pubmed-43903482015-04-21 MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region Pereira, Lloyd A. Hugo, Honor J. Malaterre, Jordane Huiling, Xu Sonza, Secondo Cures, Alina Purcell, Damian F. J. Ramsland, Paul A. Gerondakis, Steven Gonda, Thomas J. Ramsay, Robert G. PLoS One Research Article MYB transcriptional elongation is regulated by an attenuator sequence within intron 1 that has been proposed to encode a RNA stem loop (SLR) followed by a polyU tract. We report that NFκBp50 can bind the SLR polyU RNA and promote MYB transcriptional elongation together with NFκBp65. We identified a conserved lysine-rich motif within the Rel homology domain (RHD) of NFκBp50, mutation of which abrogated the interaction of NFκBp50 with the SLR polyU and impaired NFκBp50 mediated MYB elongation. We observed that the TAR RNA-binding region of Tat is homologous to the NFκBp50 RHD lysine-rich motif, a finding consistent with HIV Tat acting as an effector of MYB transcriptional elongation in an SLR dependent manner. Furthermore, we identify the DNA binding activity of NFκBp50 as a key component required for the SLR polyU mediated regulation of MYB. Collectively these results suggest that the MYB SLR polyU provides a platform for proteins to regulate MYB and reveals novel nucleic acid binding properties of NFκBp50 required for MYB regulation. Public Library of Science 2015-04-08 /pmc/articles/PMC4390348/ /pubmed/25853889 http://dx.doi.org/10.1371/journal.pone.0122919 Text en © 2015 Pereira et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pereira, Lloyd A.
Hugo, Honor J.
Malaterre, Jordane
Huiling, Xu
Sonza, Secondo
Cures, Alina
Purcell, Damian F. J.
Ramsland, Paul A.
Gerondakis, Steven
Gonda, Thomas J.
Ramsay, Robert G.
MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region
title MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region
title_full MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region
title_fullStr MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region
title_full_unstemmed MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region
title_short MYB Elongation Is Regulated by the Nucleic Acid Binding of NFκB p50 to the Intronic Stem-Loop Region
title_sort myb elongation is regulated by the nucleic acid binding of nfκb p50 to the intronic stem-loop region
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390348/
https://www.ncbi.nlm.nih.gov/pubmed/25853889
http://dx.doi.org/10.1371/journal.pone.0122919
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