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Additional Layer of Regulation via Convergent Gene Orientation in Yeasts

Convergent gene pairs can produce transcripts with complementary sequences. We had shown that mRNA duplexes form in vivo in Saccharomyces cerevisiae via interactions of mRNA overlapping 3′-ends and can lead to posttranscriptional regulatory events. Here we show that mRNA duplex formation is restrict...

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Autores principales: Gilet, Jules, Conte, Romain, Torchet, Claire, Benard, Lionel, Lafontaine, Ingrid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993858/
https://www.ncbi.nlm.nih.gov/pubmed/31580446
http://dx.doi.org/10.1093/molbev/msz221
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author Gilet, Jules
Conte, Romain
Torchet, Claire
Benard, Lionel
Lafontaine, Ingrid
author_facet Gilet, Jules
Conte, Romain
Torchet, Claire
Benard, Lionel
Lafontaine, Ingrid
author_sort Gilet, Jules
collection PubMed
description Convergent gene pairs can produce transcripts with complementary sequences. We had shown that mRNA duplexes form in vivo in Saccharomyces cerevisiae via interactions of mRNA overlapping 3′-ends and can lead to posttranscriptional regulatory events. Here we show that mRNA duplex formation is restricted to convergent genes separated by short intergenic distance, independently of their 3′-untranslated region (UTR) length. We disclose an enrichment in genes involved in biological processes related to stress among these convergent genes. They are markedly conserved in convergent orientation in budding yeasts, meaning that this mode of posttranscriptional regulation could be shared in these organisms, conferring an additional level for modulating stress response. We thus investigated the mechanistic advantages potentially conferred by 3′-UTR mRNA interactions. Analysis of genome-wide transcriptome data revealed that Pat1 and Lsm1 factors, having 3′-UTR binding preference and participating to the remodeling of messenger ribonucleoprotein particles, bind differently these messenger-interacting mRNAs forming duplexes in comparison to mRNAs that do not interact (solo mRNAs). Functionally, messenger-interacting mRNAs show limited translational repression upon stress. We thus propose that mRNA duplex formation modulates the regulation of mRNA expression by limiting their access to translational repressors. Our results thus show that posttranscriptional regulation is an additional factor that determines the order of coding genes.
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spelling pubmed-69938582020-02-05 Additional Layer of Regulation via Convergent Gene Orientation in Yeasts Gilet, Jules Conte, Romain Torchet, Claire Benard, Lionel Lafontaine, Ingrid Mol Biol Evol Discoveries Convergent gene pairs can produce transcripts with complementary sequences. We had shown that mRNA duplexes form in vivo in Saccharomyces cerevisiae via interactions of mRNA overlapping 3′-ends and can lead to posttranscriptional regulatory events. Here we show that mRNA duplex formation is restricted to convergent genes separated by short intergenic distance, independently of their 3′-untranslated region (UTR) length. We disclose an enrichment in genes involved in biological processes related to stress among these convergent genes. They are markedly conserved in convergent orientation in budding yeasts, meaning that this mode of posttranscriptional regulation could be shared in these organisms, conferring an additional level for modulating stress response. We thus investigated the mechanistic advantages potentially conferred by 3′-UTR mRNA interactions. Analysis of genome-wide transcriptome data revealed that Pat1 and Lsm1 factors, having 3′-UTR binding preference and participating to the remodeling of messenger ribonucleoprotein particles, bind differently these messenger-interacting mRNAs forming duplexes in comparison to mRNAs that do not interact (solo mRNAs). Functionally, messenger-interacting mRNAs show limited translational repression upon stress. We thus propose that mRNA duplex formation modulates the regulation of mRNA expression by limiting their access to translational repressors. Our results thus show that posttranscriptional regulation is an additional factor that determines the order of coding genes. Oxford University Press 2020-02 2019-10-03 /pmc/articles/PMC6993858/ /pubmed/31580446 http://dx.doi.org/10.1093/molbev/msz221 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Gilet, Jules
Conte, Romain
Torchet, Claire
Benard, Lionel
Lafontaine, Ingrid
Additional Layer of Regulation via Convergent Gene Orientation in Yeasts
title Additional Layer of Regulation via Convergent Gene Orientation in Yeasts
title_full Additional Layer of Regulation via Convergent Gene Orientation in Yeasts
title_fullStr Additional Layer of Regulation via Convergent Gene Orientation in Yeasts
title_full_unstemmed Additional Layer of Regulation via Convergent Gene Orientation in Yeasts
title_short Additional Layer of Regulation via Convergent Gene Orientation in Yeasts
title_sort additional layer of regulation via convergent gene orientation in yeasts
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993858/
https://www.ncbi.nlm.nih.gov/pubmed/31580446
http://dx.doi.org/10.1093/molbev/msz221
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