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The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons

The ascomycete Candida albicans is a normal resident of the gastrointestinal tract of humans and other warm-blooded animals. It occurs in a broad range of body sites and has high capacity to survive and proliferate in adverse environments with drastic changes in oxygen, carbon dioxide, pH, osmolarit...

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Autores principales: Simões, João, Bezerra, Ana R., Moura, Gabriela R., Araújo, Hugo, Gut, Ivo, Bayes, Mónica, Santos, Manuel A. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814463/
https://www.ncbi.nlm.nih.gov/pubmed/27065968
http://dx.doi.org/10.3389/fmicb.2016.00401
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author Simões, João
Bezerra, Ana R.
Moura, Gabriela R.
Araújo, Hugo
Gut, Ivo
Bayes, Mónica
Santos, Manuel A. S.
author_facet Simões, João
Bezerra, Ana R.
Moura, Gabriela R.
Araújo, Hugo
Gut, Ivo
Bayes, Mónica
Santos, Manuel A. S.
author_sort Simões, João
collection PubMed
description The ascomycete Candida albicans is a normal resident of the gastrointestinal tract of humans and other warm-blooded animals. It occurs in a broad range of body sites and has high capacity to survive and proliferate in adverse environments with drastic changes in oxygen, carbon dioxide, pH, osmolarity, nutrients, and temperature. Its biology is unique due to flexible reassignment of the leucine CUG codon to serine and synthesis of statistical proteins. Under standard growth conditions, CUG sites incorporate leucine (3% of the times) and serine (97% of the times) on a proteome wide scale, but leucine incorporation fluctuates in response to environmental stressors and can be artificially increased up to 98%. In order to determine whether such flexibility also exists at other codons, we have constructed several serine tRNAs that decode various non-cognate codons. Expression of these tRNAs had minor effects on fitness, but growth of the mistranslating strains at different temperatures, in medium with different pH and nutrients composition was often enhanced relatively to the wild type (WT) strain, supporting our previous data on adaptive roles of CUG ambiguity in variable growth conditions. Parallel evolution of the recombinant strains (100 generations) followed by full genome resequencing identified various strain specific single nucleotide polymorphisms (SNP) and one SNP in the deneddylase (JAB1) gene in all strains. Since JAB1 is a subunit of the COP9 signalosome complex, which interacts with cullin (Cdc53p) to mediate degradation of a variety of cellular proteins, our data suggest that neddylation plays a key role in tolerance and adaptation to codon ambiguity in C. albicans.
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spelling pubmed-48144632016-04-08 The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons Simões, João Bezerra, Ana R. Moura, Gabriela R. Araújo, Hugo Gut, Ivo Bayes, Mónica Santos, Manuel A. S. Front Microbiol Microbiology The ascomycete Candida albicans is a normal resident of the gastrointestinal tract of humans and other warm-blooded animals. It occurs in a broad range of body sites and has high capacity to survive and proliferate in adverse environments with drastic changes in oxygen, carbon dioxide, pH, osmolarity, nutrients, and temperature. Its biology is unique due to flexible reassignment of the leucine CUG codon to serine and synthesis of statistical proteins. Under standard growth conditions, CUG sites incorporate leucine (3% of the times) and serine (97% of the times) on a proteome wide scale, but leucine incorporation fluctuates in response to environmental stressors and can be artificially increased up to 98%. In order to determine whether such flexibility also exists at other codons, we have constructed several serine tRNAs that decode various non-cognate codons. Expression of these tRNAs had minor effects on fitness, but growth of the mistranslating strains at different temperatures, in medium with different pH and nutrients composition was often enhanced relatively to the wild type (WT) strain, supporting our previous data on adaptive roles of CUG ambiguity in variable growth conditions. Parallel evolution of the recombinant strains (100 generations) followed by full genome resequencing identified various strain specific single nucleotide polymorphisms (SNP) and one SNP in the deneddylase (JAB1) gene in all strains. Since JAB1 is a subunit of the COP9 signalosome complex, which interacts with cullin (Cdc53p) to mediate degradation of a variety of cellular proteins, our data suggest that neddylation plays a key role in tolerance and adaptation to codon ambiguity in C. albicans. Frontiers Media S.A. 2016-03-31 /pmc/articles/PMC4814463/ /pubmed/27065968 http://dx.doi.org/10.3389/fmicb.2016.00401 Text en Copyright © 2016 Simões, Bezerra, Moura, Araújo, Gut, Bayes and Santos. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Simões, João
Bezerra, Ana R.
Moura, Gabriela R.
Araújo, Hugo
Gut, Ivo
Bayes, Mónica
Santos, Manuel A. S.
The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons
title The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons
title_full The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons
title_fullStr The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons
title_full_unstemmed The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons
title_short The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons
title_sort fungus candida albicans tolerates ambiguity at multiple codons
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814463/
https://www.ncbi.nlm.nih.gov/pubmed/27065968
http://dx.doi.org/10.3389/fmicb.2016.00401
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