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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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) |
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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 |
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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 |
_version_ |
1718411841128890368 |