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Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids

The genetic code is one of the most highly conserved features across life. Only a few lineages have deviated from the “universal” genetic code. Amongst the few variants of the genetic code reported to date, the codons UAA and UAG virtually always have the same translation, suggesting that their evol...

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Autores principales: McGowan, Jamie, Kilias, Estelle S., Alacid, Elisabet, Lipscombe, James, Jenkins, Benjamin H., Gharbi, Karim, Kaithakottil, Gemy G., Macaulay, Iain C., McTaggart, Seanna, Warring, Sally D., Richards, Thomas A., Hall, Neil, Swarbreck, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553269/
https://www.ncbi.nlm.nih.gov/pubmed/37796765
http://dx.doi.org/10.1371/journal.pgen.1010913
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author McGowan, Jamie
Kilias, Estelle S.
Alacid, Elisabet
Lipscombe, James
Jenkins, Benjamin H.
Gharbi, Karim
Kaithakottil, Gemy G.
Macaulay, Iain C.
McTaggart, Seanna
Warring, Sally D.
Richards, Thomas A.
Hall, Neil
Swarbreck, David
author_facet McGowan, Jamie
Kilias, Estelle S.
Alacid, Elisabet
Lipscombe, James
Jenkins, Benjamin H.
Gharbi, Karim
Kaithakottil, Gemy G.
Macaulay, Iain C.
McTaggart, Seanna
Warring, Sally D.
Richards, Thomas A.
Hall, Neil
Swarbreck, David
author_sort McGowan, Jamie
collection PubMed
description The genetic code is one of the most highly conserved features across life. Only a few lineages have deviated from the “universal” genetic code. Amongst the few variants of the genetic code reported to date, the codons UAA and UAG virtually always have the same translation, suggesting that their evolution is coupled. Here, we report the genome and transcriptome sequencing of a novel uncultured ciliate, belonging to the Oligohymenophorea class, where the translation of the UAA and UAG stop codons have changed to specify different amino acids. Genomic and transcriptomic analyses revealed that UAA has been reassigned to encode lysine, while UAG has been reassigned to encode glutamic acid. We identified multiple suppressor tRNA genes with anticodons complementary to the reassigned codons. We show that the retained UGA stop codon is enriched in the 3’UTR immediately downstream of the coding region of genes, suggesting that there is functional drive to maintain tandem stop codons. Using a phylogenomics approach, we reconstructed the ciliate phylogeny and mapped genetic code changes, highlighting the remarkable number of independent genetic code changes within the Ciliophora group of protists. According to our knowledge, this is the first report of a genetic code variant where UAA and UAG encode different amino acids.
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spelling pubmed-105532692023-10-06 Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids McGowan, Jamie Kilias, Estelle S. Alacid, Elisabet Lipscombe, James Jenkins, Benjamin H. Gharbi, Karim Kaithakottil, Gemy G. Macaulay, Iain C. McTaggart, Seanna Warring, Sally D. Richards, Thomas A. Hall, Neil Swarbreck, David PLoS Genet Research Article The genetic code is one of the most highly conserved features across life. Only a few lineages have deviated from the “universal” genetic code. Amongst the few variants of the genetic code reported to date, the codons UAA and UAG virtually always have the same translation, suggesting that their evolution is coupled. Here, we report the genome and transcriptome sequencing of a novel uncultured ciliate, belonging to the Oligohymenophorea class, where the translation of the UAA and UAG stop codons have changed to specify different amino acids. Genomic and transcriptomic analyses revealed that UAA has been reassigned to encode lysine, while UAG has been reassigned to encode glutamic acid. We identified multiple suppressor tRNA genes with anticodons complementary to the reassigned codons. We show that the retained UGA stop codon is enriched in the 3’UTR immediately downstream of the coding region of genes, suggesting that there is functional drive to maintain tandem stop codons. Using a phylogenomics approach, we reconstructed the ciliate phylogeny and mapped genetic code changes, highlighting the remarkable number of independent genetic code changes within the Ciliophora group of protists. According to our knowledge, this is the first report of a genetic code variant where UAA and UAG encode different amino acids. Public Library of Science 2023-10-05 /pmc/articles/PMC10553269/ /pubmed/37796765 http://dx.doi.org/10.1371/journal.pgen.1010913 Text en © 2023 McGowan et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
McGowan, Jamie
Kilias, Estelle S.
Alacid, Elisabet
Lipscombe, James
Jenkins, Benjamin H.
Gharbi, Karim
Kaithakottil, Gemy G.
Macaulay, Iain C.
McTaggart, Seanna
Warring, Sally D.
Richards, Thomas A.
Hall, Neil
Swarbreck, David
Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids
title Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids
title_full Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids
title_fullStr Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids
title_full_unstemmed Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids
title_short Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids
title_sort identification of a non-canonical ciliate nuclear genetic code where uaa and uag code for different amino acids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553269/
https://www.ncbi.nlm.nih.gov/pubmed/37796765
http://dx.doi.org/10.1371/journal.pgen.1010913
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