Maturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions

Small regulatory RNAs play a major role in bacterial gene regulation by binding their target mRNAs, which mostly influences the stability or translation of the target. Expression levels of sRNAs are often regulated by their own promoters, but recent reports have highlighted the presence and importan...

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Autores principales: Daniel-Timon Spanka, Gabriele Klug
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/008dfdc8df3844ce98446c5302cd59b4
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spelling oai:doaj.org-article:008dfdc8df3844ce98446c5302cd59b42021-11-25T17:54:49ZMaturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions10.3390/ijms2222122601422-00671661-6596https://doaj.org/article/008dfdc8df3844ce98446c5302cd59b42021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/22/12260https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Small regulatory RNAs play a major role in bacterial gene regulation by binding their target mRNAs, which mostly influences the stability or translation of the target. Expression levels of sRNAs are often regulated by their own promoters, but recent reports have highlighted the presence and importance of sRNAs that are derived from mRNA 3′ untranslated regions (UTRs). In this study, we investigated the maturation of 5′ and 3′ UTR-derived sRNAs on a global scale in the facultative phototrophic alphaproteobacterium <i>Rhodobacter sphaeroides</i>. Including some already known UTR-derived sRNAs like UpsM or CcsR1-4, 14 sRNAs are predicted to be located in 5 UTRs and 16 in 3′ UTRs. The involvement of different ribonucleases during maturation was predicted by a differential RNA 5′/3′ end analysis based on RNA next generation sequencing (NGS) data from the respective deletion strains. The results were validated in vivo and underline the importance of polynucleotide phosphorylase (PNPase) and ribonuclease E (RNase E) during processing and maturation. The abundances of some UTR-derived sRNAs changed when cultures were exposed to external stress conditions, such as oxidative stress and also during different growth phases. Promoter fusions revealed that this effect cannot be solely attributed to an altered transcription rate. Moreover, the RNase E dependent cleavage of several UTR-derived sRNAs varied significantly during the early stationary phase and under iron depletion conditions. We conclude that an alteration of ribonucleolytic processing influences the levels of UTR-derived sRNAs, and may thus indirectly affect their mRNA targets.Daniel-Timon SpankaGabriele KlugMDPI AGarticleUTR-derived sRNAsRNA processing and maturationribonucleasesRNase E<i>Rhodobacter sphaeroides</i>AlphaproteobacteriaBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 12260, p 12260 (2021)
institution DOAJ
collection DOAJ
language EN
topic UTR-derived sRNA
sRNA processing and maturation
ribonucleases
RNase E
<i>Rhodobacter sphaeroides</i>
Alphaproteobacteria
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle UTR-derived sRNA
sRNA processing and maturation
ribonucleases
RNase E
<i>Rhodobacter sphaeroides</i>
Alphaproteobacteria
Biology (General)
QH301-705.5
Chemistry
QD1-999
Daniel-Timon Spanka
Gabriele Klug
Maturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions
description Small regulatory RNAs play a major role in bacterial gene regulation by binding their target mRNAs, which mostly influences the stability or translation of the target. Expression levels of sRNAs are often regulated by their own promoters, but recent reports have highlighted the presence and importance of sRNAs that are derived from mRNA 3′ untranslated regions (UTRs). In this study, we investigated the maturation of 5′ and 3′ UTR-derived sRNAs on a global scale in the facultative phototrophic alphaproteobacterium <i>Rhodobacter sphaeroides</i>. Including some already known UTR-derived sRNAs like UpsM or CcsR1-4, 14 sRNAs are predicted to be located in 5 UTRs and 16 in 3′ UTRs. The involvement of different ribonucleases during maturation was predicted by a differential RNA 5′/3′ end analysis based on RNA next generation sequencing (NGS) data from the respective deletion strains. The results were validated in vivo and underline the importance of polynucleotide phosphorylase (PNPase) and ribonuclease E (RNase E) during processing and maturation. The abundances of some UTR-derived sRNAs changed when cultures were exposed to external stress conditions, such as oxidative stress and also during different growth phases. Promoter fusions revealed that this effect cannot be solely attributed to an altered transcription rate. Moreover, the RNase E dependent cleavage of several UTR-derived sRNAs varied significantly during the early stationary phase and under iron depletion conditions. We conclude that an alteration of ribonucleolytic processing influences the levels of UTR-derived sRNAs, and may thus indirectly affect their mRNA targets.
format article
author Daniel-Timon Spanka
Gabriele Klug
author_facet Daniel-Timon Spanka
Gabriele Klug
author_sort Daniel-Timon Spanka
title Maturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions
title_short Maturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions
title_full Maturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions
title_fullStr Maturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions
title_full_unstemmed Maturation of UTR-Derived sRNAs Is Modulated during Adaptation to Different Growth Conditions
title_sort maturation of utr-derived srnas is modulated during adaptation to different growth conditions
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/008dfdc8df3844ce98446c5302cd59b4
work_keys_str_mv AT danieltimonspanka maturationofutrderivedsrnasismodulatedduringadaptationtodifferentgrowthconditions
AT gabrieleklug maturationofutrderivedsrnasismodulatedduringadaptationtodifferentgrowthconditions
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