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Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium

Exposure to abiotic stresses triggers global changes in the expression of thousands of eukaryotic genes at the transcriptional and post-transcriptional levels. Small RNA (smRNA) pathways and splicing both function as crucial mechanisms regulating stress-responsive gene expression. However, examples...

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Autores principales: Wang, Hsiao-Lin V., Dinwiddie, Brandon L., Lee, Herman, Chekanova, Julia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338343/
https://www.ncbi.nlm.nih.gov/pubmed/25480817
http://dx.doi.org/10.1261/rna.047662.114
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author Wang, Hsiao-Lin V.
Dinwiddie, Brandon L.
Lee, Herman
Chekanova, Julia A.
author_facet Wang, Hsiao-Lin V.
Dinwiddie, Brandon L.
Lee, Herman
Chekanova, Julia A.
author_sort Wang, Hsiao-Lin V.
collection PubMed
description Exposure to abiotic stresses triggers global changes in the expression of thousands of eukaryotic genes at the transcriptional and post-transcriptional levels. Small RNA (smRNA) pathways and splicing both function as crucial mechanisms regulating stress-responsive gene expression. However, examples of smRNAs regulating gene expression remain largely limited to effects on mRNA stability, translation, and epigenetic regulation. Also, our understanding of the networks controlling plant gene expression in response to environmental changes, and examples of these regulatory pathways intersecting, remains limited. Here, to investigate the role of smRNAs in stress responses we examined smRNA transcriptomes of Brachypodium distachyon plants subjected to various abiotic stresses. We found that exposure to different abiotic stresses specifically induced a group of novel, endogenous small interfering RNAs (stress-induced, UTR-derived siRNAs, or sutr-siRNAs) that originate from the 3′ UTRs of a subset of coding genes. Our bioinformatics analyses predicted that sutr-siRNAs have potential regulatory functions and that over 90% of sutr-siRNAs target intronic regions of many mRNAs in trans. Importantly, a subgroup of these sutr-siRNAs target the important intron regulatory regions, such as branch point sequences, that could affect splicing. Our study indicates that in Brachypodium, sutr-siRNAs may affect splicing by masking or changing accessibility of specific cis-elements through base-pairing interactions to mediate gene expression in response to stresses. We hypothesize that this mode of regulation of gene expression may also serve as a general mechanism for regulation of gene expression in plants and potentially in other eukaryotes.
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spelling pubmed-43383432016-02-01 Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium Wang, Hsiao-Lin V. Dinwiddie, Brandon L. Lee, Herman Chekanova, Julia A. RNA Bioinformatics Exposure to abiotic stresses triggers global changes in the expression of thousands of eukaryotic genes at the transcriptional and post-transcriptional levels. Small RNA (smRNA) pathways and splicing both function as crucial mechanisms regulating stress-responsive gene expression. However, examples of smRNAs regulating gene expression remain largely limited to effects on mRNA stability, translation, and epigenetic regulation. Also, our understanding of the networks controlling plant gene expression in response to environmental changes, and examples of these regulatory pathways intersecting, remains limited. Here, to investigate the role of smRNAs in stress responses we examined smRNA transcriptomes of Brachypodium distachyon plants subjected to various abiotic stresses. We found that exposure to different abiotic stresses specifically induced a group of novel, endogenous small interfering RNAs (stress-induced, UTR-derived siRNAs, or sutr-siRNAs) that originate from the 3′ UTRs of a subset of coding genes. Our bioinformatics analyses predicted that sutr-siRNAs have potential regulatory functions and that over 90% of sutr-siRNAs target intronic regions of many mRNAs in trans. Importantly, a subgroup of these sutr-siRNAs target the important intron regulatory regions, such as branch point sequences, that could affect splicing. Our study indicates that in Brachypodium, sutr-siRNAs may affect splicing by masking or changing accessibility of specific cis-elements through base-pairing interactions to mediate gene expression in response to stresses. We hypothesize that this mode of regulation of gene expression may also serve as a general mechanism for regulation of gene expression in plants and potentially in other eukaryotes. Cold Spring Harbor Laboratory Press 2015-02 /pmc/articles/PMC4338343/ /pubmed/25480817 http://dx.doi.org/10.1261/rna.047662.114 Text en © 2015 Wang et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Bioinformatics
Wang, Hsiao-Lin V.
Dinwiddie, Brandon L.
Lee, Herman
Chekanova, Julia A.
Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium
title Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium
title_full Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium
title_fullStr Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium
title_full_unstemmed Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium
title_short Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium
title_sort stress-induced endogenous sirnas targeting regulatory intron sequences in brachypodium
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338343/
https://www.ncbi.nlm.nih.gov/pubmed/25480817
http://dx.doi.org/10.1261/rna.047662.114
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