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Virus infection elevates transcriptional activity of miR164a promoter in plants

BACKGROUND: Micro RNAs (miRs) constitute a large group of endogenous small RNAs that have crucial roles in many important plant functions. Virus infection and transgenic expression of viral proteins alter accumulation and activity of miRs and so far, most of the published evidence involves post-tran...

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Autores principales: Bazzini, Ariel A, Almasia, Natalia I, Manacorda, Carlos A, Mongelli, Vanesa C, Conti, Gabriela, Maroniche, Guillermo A, Rodriguez, María C, Distéfano, Ana J, Hopp, H Esteban, del Vas, Mariana, Asurmendi, Sebastian
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809068/
https://www.ncbi.nlm.nih.gov/pubmed/20042107
http://dx.doi.org/10.1186/1471-2229-9-152
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author Bazzini, Ariel A
Almasia, Natalia I
Manacorda, Carlos A
Mongelli, Vanesa C
Conti, Gabriela
Maroniche, Guillermo A
Rodriguez, María C
Distéfano, Ana J
Hopp, H Esteban
del Vas, Mariana
Asurmendi, Sebastian
author_facet Bazzini, Ariel A
Almasia, Natalia I
Manacorda, Carlos A
Mongelli, Vanesa C
Conti, Gabriela
Maroniche, Guillermo A
Rodriguez, María C
Distéfano, Ana J
Hopp, H Esteban
del Vas, Mariana
Asurmendi, Sebastian
author_sort Bazzini, Ariel A
collection PubMed
description BACKGROUND: Micro RNAs (miRs) constitute a large group of endogenous small RNAs that have crucial roles in many important plant functions. Virus infection and transgenic expression of viral proteins alter accumulation and activity of miRs and so far, most of the published evidence involves post-transcriptional regulations. RESULTS: Using transgenic plants expressing a reporter gene under the promoter region of a characterized miR (P-miR164a), we monitored the reporter gene expression in different tissues and during Arabidopsis development. Strong expression was detected in both vascular tissues and hydathodes. P-miR164a activity was developmentally regulated in plants with a maximum expression at stages 1.12 to 5.1 (according to Boyes, 2001) along the transition from vegetative to reproductive growth. Upon quantification of P-miR164a-derived GUS activity after Tobacco mosaic virus Cg or Oilseed rape mosaic virus (ORMV) infection and after hormone treatments, we demonstrated that ORMV and gibberellic acid elevated P-miR164a activity. Accordingly, total mature miR164, precursor of miR164a and CUC1 mRNA (a miR164 target) levels increased after virus infection and interestingly the most severe virus (ORMV) produced the strongest promoter induction. CONCLUSION: This work shows for the first time that the alteration of miR pathways produced by viral infections possesses a transcriptional component. In addition, the degree of miR alteration correlates with virus severity since a more severe virus produces a stronger P-miR164a induction.
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spelling pubmed-28090682010-01-21 Virus infection elevates transcriptional activity of miR164a promoter in plants Bazzini, Ariel A Almasia, Natalia I Manacorda, Carlos A Mongelli, Vanesa C Conti, Gabriela Maroniche, Guillermo A Rodriguez, María C Distéfano, Ana J Hopp, H Esteban del Vas, Mariana Asurmendi, Sebastian BMC Plant Biol Research article BACKGROUND: Micro RNAs (miRs) constitute a large group of endogenous small RNAs that have crucial roles in many important plant functions. Virus infection and transgenic expression of viral proteins alter accumulation and activity of miRs and so far, most of the published evidence involves post-transcriptional regulations. RESULTS: Using transgenic plants expressing a reporter gene under the promoter region of a characterized miR (P-miR164a), we monitored the reporter gene expression in different tissues and during Arabidopsis development. Strong expression was detected in both vascular tissues and hydathodes. P-miR164a activity was developmentally regulated in plants with a maximum expression at stages 1.12 to 5.1 (according to Boyes, 2001) along the transition from vegetative to reproductive growth. Upon quantification of P-miR164a-derived GUS activity after Tobacco mosaic virus Cg or Oilseed rape mosaic virus (ORMV) infection and after hormone treatments, we demonstrated that ORMV and gibberellic acid elevated P-miR164a activity. Accordingly, total mature miR164, precursor of miR164a and CUC1 mRNA (a miR164 target) levels increased after virus infection and interestingly the most severe virus (ORMV) produced the strongest promoter induction. CONCLUSION: This work shows for the first time that the alteration of miR pathways produced by viral infections possesses a transcriptional component. In addition, the degree of miR alteration correlates with virus severity since a more severe virus produces a stronger P-miR164a induction. BioMed Central 2009-12-30 /pmc/articles/PMC2809068/ /pubmed/20042107 http://dx.doi.org/10.1186/1471-2229-9-152 Text en Copyright ©2009 Bazzini et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Bazzini, Ariel A
Almasia, Natalia I
Manacorda, Carlos A
Mongelli, Vanesa C
Conti, Gabriela
Maroniche, Guillermo A
Rodriguez, María C
Distéfano, Ana J
Hopp, H Esteban
del Vas, Mariana
Asurmendi, Sebastian
Virus infection elevates transcriptional activity of miR164a promoter in plants
title Virus infection elevates transcriptional activity of miR164a promoter in plants
title_full Virus infection elevates transcriptional activity of miR164a promoter in plants
title_fullStr Virus infection elevates transcriptional activity of miR164a promoter in plants
title_full_unstemmed Virus infection elevates transcriptional activity of miR164a promoter in plants
title_short Virus infection elevates transcriptional activity of miR164a promoter in plants
title_sort virus infection elevates transcriptional activity of mir164a promoter in plants
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809068/
https://www.ncbi.nlm.nih.gov/pubmed/20042107
http://dx.doi.org/10.1186/1471-2229-9-152
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