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Distinct responses to rare codons in select Drosophila tissues

Codon usage bias has long been appreciated to influence protein production. Yet, relatively few studies have analyzed the impacts of codon usage on tissue-specific mRNA and protein expression. Here, we use codon-modified reporters to perform an organism-wide screen in Drosophila melanogaster for dis...

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Autores principales: Allen, Scott R, Stewart, Rebeccah K, Rogers, Michael, Ruiz, Ivan Jimenez, Cohen, Erez, Laederach, Alain, Counter, Christopher M, Sawyer, Jessica K, Fox, Donald T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116940/
https://www.ncbi.nlm.nih.gov/pubmed/35522036
http://dx.doi.org/10.7554/eLife.76893
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author Allen, Scott R
Stewart, Rebeccah K
Rogers, Michael
Ruiz, Ivan Jimenez
Cohen, Erez
Laederach, Alain
Counter, Christopher M
Sawyer, Jessica K
Fox, Donald T
author_facet Allen, Scott R
Stewart, Rebeccah K
Rogers, Michael
Ruiz, Ivan Jimenez
Cohen, Erez
Laederach, Alain
Counter, Christopher M
Sawyer, Jessica K
Fox, Donald T
author_sort Allen, Scott R
collection PubMed
description Codon usage bias has long been appreciated to influence protein production. Yet, relatively few studies have analyzed the impacts of codon usage on tissue-specific mRNA and protein expression. Here, we use codon-modified reporters to perform an organism-wide screen in Drosophila melanogaster for distinct tissue responses to codon usage bias. These reporters reveal a cliff-like decline of protein expression near the limit of rare codon usage in endogenously expressed Drosophila genes. Near the edge of this limit, however, we find the testis and brain are uniquely capable of expressing rare codon-enriched reporters. We define a new metric of tissue-specific codon usage, the tissue-apparent Codon Adaptation Index (taCAI), to reveal a conserved enrichment for rare codon usage in the endogenously expressed genes of both Drosophila and human testis. We further demonstrate a role for rare codons in an evolutionarily young testis-specific gene, RpL10Aa. Optimizing RpL10Aa codons disrupts female fertility. Our work highlights distinct responses to rarely used codons in select tissues, revealing a critical role for codon bias in tissue biology.
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spelling pubmed-91169402022-05-19 Distinct responses to rare codons in select Drosophila tissues Allen, Scott R Stewart, Rebeccah K Rogers, Michael Ruiz, Ivan Jimenez Cohen, Erez Laederach, Alain Counter, Christopher M Sawyer, Jessica K Fox, Donald T eLife Developmental Biology Codon usage bias has long been appreciated to influence protein production. Yet, relatively few studies have analyzed the impacts of codon usage on tissue-specific mRNA and protein expression. Here, we use codon-modified reporters to perform an organism-wide screen in Drosophila melanogaster for distinct tissue responses to codon usage bias. These reporters reveal a cliff-like decline of protein expression near the limit of rare codon usage in endogenously expressed Drosophila genes. Near the edge of this limit, however, we find the testis and brain are uniquely capable of expressing rare codon-enriched reporters. We define a new metric of tissue-specific codon usage, the tissue-apparent Codon Adaptation Index (taCAI), to reveal a conserved enrichment for rare codon usage in the endogenously expressed genes of both Drosophila and human testis. We further demonstrate a role for rare codons in an evolutionarily young testis-specific gene, RpL10Aa. Optimizing RpL10Aa codons disrupts female fertility. Our work highlights distinct responses to rarely used codons in select tissues, revealing a critical role for codon bias in tissue biology. eLife Sciences Publications, Ltd 2022-05-06 /pmc/articles/PMC9116940/ /pubmed/35522036 http://dx.doi.org/10.7554/eLife.76893 Text en © 2022, Allen et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Allen, Scott R
Stewart, Rebeccah K
Rogers, Michael
Ruiz, Ivan Jimenez
Cohen, Erez
Laederach, Alain
Counter, Christopher M
Sawyer, Jessica K
Fox, Donald T
Distinct responses to rare codons in select Drosophila tissues
title Distinct responses to rare codons in select Drosophila tissues
title_full Distinct responses to rare codons in select Drosophila tissues
title_fullStr Distinct responses to rare codons in select Drosophila tissues
title_full_unstemmed Distinct responses to rare codons in select Drosophila tissues
title_short Distinct responses to rare codons in select Drosophila tissues
title_sort distinct responses to rare codons in select drosophila tissues
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116940/
https://www.ncbi.nlm.nih.gov/pubmed/35522036
http://dx.doi.org/10.7554/eLife.76893
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