Salt stress affects mRNA editing in soybean chloroplasts

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Nureyev Ferreira
Data de Publicação: 2017
Outros Autores: Fonseca, Guilherme Cordenonsi da, Kulcheski, Franceli Rodrigues, Margis, Rogerio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/166148
Resumo: Soybean, a crop known by its economic and nutritional importance, has been the subject of several studies that assess the impact and the effective plant responses to abiotic stresses. Salt stress is one of the main environmental stresses and negatively impacts crop growth and yield. In this work, the RNA editing process in the chloroplast of soybean plants was evaluated in response to a salt stress. Bioinformatics approach using sRNA and mRNA libraries were employed to detect specific sites showing differences in editing efficiency. RT-qPCR was used to measure editing efficiency at selected sites. We observed that transcripts of NDHA, NDHB, RPS14 and RPS16 genes presented differences in coverage and editing rates between control and salt-treated libraries. RT-qPCR assays demonstrated an increase in editing efficiency of selected genes. The salt stress enhanced the RNA editing process in transcripts, indicating responses to components of the electron transfer chain, photosystem and translation complexes. These increases can be a response to keep the homeostasis of chloroplast protein functions in response to salt stress.
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spelling Rodrigues, Nureyev FerreiraFonseca, Guilherme Cordenonsi daKulcheski, Franceli RodriguesMargis, Rogerio2017-09-05T02:32:40Z20171415-4757http://hdl.handle.net/10183/166148001026700Soybean, a crop known by its economic and nutritional importance, has been the subject of several studies that assess the impact and the effective plant responses to abiotic stresses. Salt stress is one of the main environmental stresses and negatively impacts crop growth and yield. In this work, the RNA editing process in the chloroplast of soybean plants was evaluated in response to a salt stress. Bioinformatics approach using sRNA and mRNA libraries were employed to detect specific sites showing differences in editing efficiency. RT-qPCR was used to measure editing efficiency at selected sites. We observed that transcripts of NDHA, NDHB, RPS14 and RPS16 genes presented differences in coverage and editing rates between control and salt-treated libraries. RT-qPCR assays demonstrated an increase in editing efficiency of selected genes. The salt stress enhanced the RNA editing process in transcripts, indicating responses to components of the electron transfer chain, photosystem and translation complexes. These increases can be a response to keep the homeostasis of chloroplast protein functions in response to salt stress.application/pdfengGenetics and molecular biology. Ribeirão Preto, SP. Vol. 40, no. 1, suppl. 1 (2017), p. 200-208RNACloroplastoEstresse salinoSmall RNAChloroplastRNA editingPPRSalt stressSalt stress affects mRNA editing in soybean chloroplastsinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001026700.pdf001026700.pdfTexto completo (inglês)application/pdf867262http://www.lume.ufrgs.br/bitstream/10183/166148/1/001026700.pdf8ee4bc849e4515c2f229b84468461653MD51TEXT001026700.pdf.txt001026700.pdf.txtExtracted Texttext/plain39406http://www.lume.ufrgs.br/bitstream/10183/166148/2/001026700.pdf.txt17613059d0323e110f23cf2a2ed48df1MD52THUMBNAIL001026700.pdf.jpg001026700.pdf.jpgGenerated Thumbnailimage/jpeg1832http://www.lume.ufrgs.br/bitstream/10183/166148/3/001026700.pdf.jpg0f67954fec687d5eb3c78ed15020d830MD5310183/1661482021-09-18 04:49:39.9oai:www.lume.ufrgs.br:10183/166148Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-18T07:49:39Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Salt stress affects mRNA editing in soybean chloroplasts
title Salt stress affects mRNA editing in soybean chloroplasts
spellingShingle Salt stress affects mRNA editing in soybean chloroplasts
Rodrigues, Nureyev Ferreira
RNA
Cloroplasto
Estresse salino
Small RNA
Chloroplast
RNA editing
PPR
Salt stress
title_short Salt stress affects mRNA editing in soybean chloroplasts
title_full Salt stress affects mRNA editing in soybean chloroplasts
title_fullStr Salt stress affects mRNA editing in soybean chloroplasts
title_full_unstemmed Salt stress affects mRNA editing in soybean chloroplasts
title_sort Salt stress affects mRNA editing in soybean chloroplasts
author Rodrigues, Nureyev Ferreira
author_facet Rodrigues, Nureyev Ferreira
Fonseca, Guilherme Cordenonsi da
Kulcheski, Franceli Rodrigues
Margis, Rogerio
author_role author
author2 Fonseca, Guilherme Cordenonsi da
Kulcheski, Franceli Rodrigues
Margis, Rogerio
author2_role author
author
author
dc.contributor.author.fl_str_mv Rodrigues, Nureyev Ferreira
Fonseca, Guilherme Cordenonsi da
Kulcheski, Franceli Rodrigues
Margis, Rogerio
dc.subject.por.fl_str_mv RNA
Cloroplasto
Estresse salino
topic RNA
Cloroplasto
Estresse salino
Small RNA
Chloroplast
RNA editing
PPR
Salt stress
dc.subject.eng.fl_str_mv Small RNA
Chloroplast
RNA editing
PPR
Salt stress
description Soybean, a crop known by its economic and nutritional importance, has been the subject of several studies that assess the impact and the effective plant responses to abiotic stresses. Salt stress is one of the main environmental stresses and negatively impacts crop growth and yield. In this work, the RNA editing process in the chloroplast of soybean plants was evaluated in response to a salt stress. Bioinformatics approach using sRNA and mRNA libraries were employed to detect specific sites showing differences in editing efficiency. RT-qPCR was used to measure editing efficiency at selected sites. We observed that transcripts of NDHA, NDHB, RPS14 and RPS16 genes presented differences in coverage and editing rates between control and salt-treated libraries. RT-qPCR assays demonstrated an increase in editing efficiency of selected genes. The salt stress enhanced the RNA editing process in transcripts, indicating responses to components of the electron transfer chain, photosystem and translation complexes. These increases can be a response to keep the homeostasis of chloroplast protein functions in response to salt stress.
publishDate 2017
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Genetics and molecular biology. Ribeirão Preto, SP. Vol. 40, no. 1, suppl. 1 (2017), p. 200-208
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