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Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences

BACKGROUND: The 3′ untranslated region (UTR) plays critical roles in determining the level of gene expression through effects on activities such as mRNA stability and translation. Functional elements within this region have largely been identified through analyses of native genes, which contain mult...

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Autores principales: Savinov, Andrew, Brandsen, Benjamin M., Angell, Brooke E., Cuperus, Josh T., Fields, Stanley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522215/
https://www.ncbi.nlm.nih.gov/pubmed/34663436
http://dx.doi.org/10.1186/s13059-021-02509-6
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author Savinov, Andrew
Brandsen, Benjamin M.
Angell, Brooke E.
Cuperus, Josh T.
Fields, Stanley
author_facet Savinov, Andrew
Brandsen, Benjamin M.
Angell, Brooke E.
Cuperus, Josh T.
Fields, Stanley
author_sort Savinov, Andrew
collection PubMed
description BACKGROUND: The 3′ untranslated region (UTR) plays critical roles in determining the level of gene expression through effects on activities such as mRNA stability and translation. Functional elements within this region have largely been identified through analyses of native genes, which contain multiple co-evolved sequence features. RESULTS: To explore the effects of 3′ UTR sequence elements outside of native sequence contexts, we analyze hundreds of thousands of random 50-mers inserted into the 3′ UTR of a reporter gene in the yeast Saccharomyces cerevisiae. We determine relative protein expression levels from the fitness of transformants in a growth selection. We find that the consensus 3′ UTR efficiency element significantly boosts expression, independent of sequence context; on the other hand, the consensus positioning element has only a small effect on expression. Some sequence motifs that are binding sites for Puf proteins substantially increase expression in the library, despite these proteins generally being associated with post-transcriptional downregulation of native mRNAs. Our measurements also allow a systematic examination of the effects of point mutations within efficiency element motifs across diverse sequence backgrounds. These mutational scans reveal the relative in vivo importance of individual bases in the efficiency element, which likely reflects their roles in binding the Hrp1 protein involved in cleavage and polyadenylation. CONCLUSIONS: The regulatory effects of some 3′ UTR sequence features, like the efficiency element, are consistent regardless of sequence context. In contrast, the consequences of other 3′ UTR features appear to be strongly dependent on their evolved context within native genes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02509-6.
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spelling pubmed-85222152021-10-21 Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences Savinov, Andrew Brandsen, Benjamin M. Angell, Brooke E. Cuperus, Josh T. Fields, Stanley Genome Biol Research BACKGROUND: The 3′ untranslated region (UTR) plays critical roles in determining the level of gene expression through effects on activities such as mRNA stability and translation. Functional elements within this region have largely been identified through analyses of native genes, which contain multiple co-evolved sequence features. RESULTS: To explore the effects of 3′ UTR sequence elements outside of native sequence contexts, we analyze hundreds of thousands of random 50-mers inserted into the 3′ UTR of a reporter gene in the yeast Saccharomyces cerevisiae. We determine relative protein expression levels from the fitness of transformants in a growth selection. We find that the consensus 3′ UTR efficiency element significantly boosts expression, independent of sequence context; on the other hand, the consensus positioning element has only a small effect on expression. Some sequence motifs that are binding sites for Puf proteins substantially increase expression in the library, despite these proteins generally being associated with post-transcriptional downregulation of native mRNAs. Our measurements also allow a systematic examination of the effects of point mutations within efficiency element motifs across diverse sequence backgrounds. These mutational scans reveal the relative in vivo importance of individual bases in the efficiency element, which likely reflects their roles in binding the Hrp1 protein involved in cleavage and polyadenylation. CONCLUSIONS: The regulatory effects of some 3′ UTR sequence features, like the efficiency element, are consistent regardless of sequence context. In contrast, the consequences of other 3′ UTR features appear to be strongly dependent on their evolved context within native genes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02509-6. BioMed Central 2021-10-18 /pmc/articles/PMC8522215/ /pubmed/34663436 http://dx.doi.org/10.1186/s13059-021-02509-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Savinov, Andrew
Brandsen, Benjamin M.
Angell, Brooke E.
Cuperus, Josh T.
Fields, Stanley
Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences
title Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences
title_full Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences
title_fullStr Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences
title_full_unstemmed Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences
title_short Effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences
title_sort effects of sequence motifs in the yeast 3′ untranslated region determined from massively parallel assays of random sequences
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522215/
https://www.ncbi.nlm.nih.gov/pubmed/34663436
http://dx.doi.org/10.1186/s13059-021-02509-6
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