Cargando…

Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection

MicroRNAs (miRNAs) have been well known to play diverse roles in viral infection at the level of posttranscriptional repression. However, much less is understood about the mechanism by which miRNAs are regulated during viral infection. It is likely that both host and virus contain factors to modulat...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Bibo, Ye, Jing, Ashraf, Usama, Li, Yunchuan, Chen, Huanchun, Song, Yunfeng, Cao, Shengbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773857/
https://www.ncbi.nlm.nih.gov/pubmed/26931521
http://dx.doi.org/10.1038/srep22581
_version_ 1782418821453185024
author Zhu, Bibo
Ye, Jing
Ashraf, Usama
Li, Yunchuan
Chen, Huanchun
Song, Yunfeng
Cao, Shengbo
author_facet Zhu, Bibo
Ye, Jing
Ashraf, Usama
Li, Yunchuan
Chen, Huanchun
Song, Yunfeng
Cao, Shengbo
author_sort Zhu, Bibo
collection PubMed
description MicroRNAs (miRNAs) have been well known to play diverse roles in viral infection at the level of posttranscriptional repression. However, much less is understood about the mechanism by which miRNAs are regulated during viral infection. It is likely that both host and virus contain factors to modulate miRNA expression. Here we report the up-regulation of microRNA-15b (miR-15b) in vitro upon infection with Japanese encephalitis virus (JEV). Analysis of miR-15b precursor, pri-miR-15b and pre-miR-15b, suggest that the regulation occurs transcriptionally. Further, we identified the transcriptional regulatory region of miR-15b that contains consensus binding motif for NF-κB subunit c-Rel and cAMP-response element binding protein (CREB), which are known as transcription factor to regulate gene expression. By promoter fusion and mutational analyses, we demonstrated that c-Rel and CREB bind directly to the promoter elements of miR-15b, which are responsible for miR-15b transcription in response to JEV infection. Finally, we showed that pharmacological inhibition of ERK and NF-κB signaling pathway blocked induction of miR-15b in JEV infection, suggesting important roles of ERK and NF-κB pathway in the regulation of miR-15b gene. Therefore, our observations indicate that induced expression of miR-15b is modulated by c-Rel and CREB in response to JEV infection.
format Online
Article
Text
id pubmed-4773857
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-47738572016-03-09 Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection Zhu, Bibo Ye, Jing Ashraf, Usama Li, Yunchuan Chen, Huanchun Song, Yunfeng Cao, Shengbo Sci Rep Article MicroRNAs (miRNAs) have been well known to play diverse roles in viral infection at the level of posttranscriptional repression. However, much less is understood about the mechanism by which miRNAs are regulated during viral infection. It is likely that both host and virus contain factors to modulate miRNA expression. Here we report the up-regulation of microRNA-15b (miR-15b) in vitro upon infection with Japanese encephalitis virus (JEV). Analysis of miR-15b precursor, pri-miR-15b and pre-miR-15b, suggest that the regulation occurs transcriptionally. Further, we identified the transcriptional regulatory region of miR-15b that contains consensus binding motif for NF-κB subunit c-Rel and cAMP-response element binding protein (CREB), which are known as transcription factor to regulate gene expression. By promoter fusion and mutational analyses, we demonstrated that c-Rel and CREB bind directly to the promoter elements of miR-15b, which are responsible for miR-15b transcription in response to JEV infection. Finally, we showed that pharmacological inhibition of ERK and NF-κB signaling pathway blocked induction of miR-15b in JEV infection, suggesting important roles of ERK and NF-κB pathway in the regulation of miR-15b gene. Therefore, our observations indicate that induced expression of miR-15b is modulated by c-Rel and CREB in response to JEV infection. Nature Publishing Group 2016-03-02 /pmc/articles/PMC4773857/ /pubmed/26931521 http://dx.doi.org/10.1038/srep22581 Text en Copyright © 2016, Macmillan Publishers Limited 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
Zhu, Bibo
Ye, Jing
Ashraf, Usama
Li, Yunchuan
Chen, Huanchun
Song, Yunfeng
Cao, Shengbo
Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection
title Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection
title_full Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection
title_fullStr Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection
title_full_unstemmed Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection
title_short Transcriptional regulation of miR-15b by c-Rel and CREB in Japanese encephalitis virus infection
title_sort transcriptional regulation of mir-15b by c-rel and creb in japanese encephalitis virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773857/
https://www.ncbi.nlm.nih.gov/pubmed/26931521
http://dx.doi.org/10.1038/srep22581
work_keys_str_mv AT zhubibo transcriptionalregulationofmir15bbycrelandcrebinjapaneseencephalitisvirusinfection
AT yejing transcriptionalregulationofmir15bbycrelandcrebinjapaneseencephalitisvirusinfection
AT ashrafusama transcriptionalregulationofmir15bbycrelandcrebinjapaneseencephalitisvirusinfection
AT liyunchuan transcriptionalregulationofmir15bbycrelandcrebinjapaneseencephalitisvirusinfection
AT chenhuanchun transcriptionalregulationofmir15bbycrelandcrebinjapaneseencephalitisvirusinfection
AT songyunfeng transcriptionalregulationofmir15bbycrelandcrebinjapaneseencephalitisvirusinfection
AT caoshengbo transcriptionalregulationofmir15bbycrelandcrebinjapaneseencephalitisvirusinfection