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The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism

The E1B 55kDa produced by human adenovirus type 5 is a multifunctional protein that participates in the regulation of several steps during the viral replication cycle. Previous studies suggest this protein plays an important role in postranscriptional regulation of viral and cellular gene expression...

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Autores principales: Tejera, Berto, López, Raúl E., Hidalgo, Paloma, Cárdenas, Reinier, Ballesteros, Grisel, Rivillas, Lina, French, Leidys, Amero, Carlos, Pastor, Nina, Santiago, Ángel, Groitl, Peter, Dobner, Thomas, Gonzalez, Ramón A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447194/
https://www.ncbi.nlm.nih.gov/pubmed/30943256
http://dx.doi.org/10.1371/journal.pone.0214882
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author Tejera, Berto
López, Raúl E.
Hidalgo, Paloma
Cárdenas, Reinier
Ballesteros, Grisel
Rivillas, Lina
French, Leidys
Amero, Carlos
Pastor, Nina
Santiago, Ángel
Groitl, Peter
Dobner, Thomas
Gonzalez, Ramón A.
author_facet Tejera, Berto
López, Raúl E.
Hidalgo, Paloma
Cárdenas, Reinier
Ballesteros, Grisel
Rivillas, Lina
French, Leidys
Amero, Carlos
Pastor, Nina
Santiago, Ángel
Groitl, Peter
Dobner, Thomas
Gonzalez, Ramón A.
author_sort Tejera, Berto
collection PubMed
description The E1B 55kDa produced by human adenovirus type 5 is a multifunctional protein that participates in the regulation of several steps during the viral replication cycle. Previous studies suggest this protein plays an important role in postranscriptional regulation of viral and cellular gene expression, as it is required for the selective accumulation of maximal levels of viral late mRNA in the cytoplasm of the infected cell; however the molecular mechanisms that are altered or regulated by this protein have not been elucidated. A ribonucleoprotein motif that could implicate the direct interaction of the protein with RNA was initially predicted and tested in vitro, but the interaction with RNA could not be detected in infected cells, suggesting the interaction may be weak or transient. Here it was determined that the E1B 55kDa interacts with RNA in the context of the viral infection in non-transformed human cells, and its contribution to the adenovirus replication cycle was evaluated. Using recombinant adenoviruses with amino acid substitutions or a deletion in the ribonucleoprotein motif the interaction of E1B 55kDa with RNA was found to correlate with timely and efficient viral DNA replication and viral late mRNA accumulation and splicing.
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spelling pubmed-64471942019-04-17 The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism Tejera, Berto López, Raúl E. Hidalgo, Paloma Cárdenas, Reinier Ballesteros, Grisel Rivillas, Lina French, Leidys Amero, Carlos Pastor, Nina Santiago, Ángel Groitl, Peter Dobner, Thomas Gonzalez, Ramón A. PLoS One Research Article The E1B 55kDa produced by human adenovirus type 5 is a multifunctional protein that participates in the regulation of several steps during the viral replication cycle. Previous studies suggest this protein plays an important role in postranscriptional regulation of viral and cellular gene expression, as it is required for the selective accumulation of maximal levels of viral late mRNA in the cytoplasm of the infected cell; however the molecular mechanisms that are altered or regulated by this protein have not been elucidated. A ribonucleoprotein motif that could implicate the direct interaction of the protein with RNA was initially predicted and tested in vitro, but the interaction with RNA could not be detected in infected cells, suggesting the interaction may be weak or transient. Here it was determined that the E1B 55kDa interacts with RNA in the context of the viral infection in non-transformed human cells, and its contribution to the adenovirus replication cycle was evaluated. Using recombinant adenoviruses with amino acid substitutions or a deletion in the ribonucleoprotein motif the interaction of E1B 55kDa with RNA was found to correlate with timely and efficient viral DNA replication and viral late mRNA accumulation and splicing. Public Library of Science 2019-04-03 /pmc/articles/PMC6447194/ /pubmed/30943256 http://dx.doi.org/10.1371/journal.pone.0214882 Text en © 2019 Tejera 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tejera, Berto
López, Raúl E.
Hidalgo, Paloma
Cárdenas, Reinier
Ballesteros, Grisel
Rivillas, Lina
French, Leidys
Amero, Carlos
Pastor, Nina
Santiago, Ángel
Groitl, Peter
Dobner, Thomas
Gonzalez, Ramón A.
The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism
title The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism
title_full The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism
title_fullStr The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism
title_full_unstemmed The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism
title_short The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism
title_sort human adenovirus type 5 e1b 55kda protein interacts with rna promoting timely dna replication and viral late mrna metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447194/
https://www.ncbi.nlm.nih.gov/pubmed/30943256
http://dx.doi.org/10.1371/journal.pone.0214882
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