Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.

The translation of nucleotide sequences into amino acid sequences, governed by the genetic code, is one of the most conserved features of molecular biology. The standard genetic code, which uses 61 sense codons to encode one of the 20 standard amino acids and 3 stop codons (UAA, UAG, and UGA) to ter...

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Main Authors: Jamie McGowan, Thomas A Richards, Neil Hall, David Swarbreck
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2024-12-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1011512
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author Jamie McGowan
Thomas A Richards
Neil Hall
David Swarbreck
author_facet Jamie McGowan
Thomas A Richards
Neil Hall
David Swarbreck
author_sort Jamie McGowan
collection DOAJ
description The translation of nucleotide sequences into amino acid sequences, governed by the genetic code, is one of the most conserved features of molecular biology. The standard genetic code, which uses 61 sense codons to encode one of the 20 standard amino acids and 3 stop codons (UAA, UAG, and UGA) to terminate translation, is used by most extant organisms. The protistan phylum Ciliophora (the 'ciliates') are the most prominent exception to this norm, exhibiting the grfeatest diversity of nuclear genetic code variants and evidence of repeated changes in the code. In this study, we report the discovery of multiple independent genetic code changes within the Phyllopharyngea class of ciliates. By mining publicly available ciliate genome datasets, we discovered that three ciliate species from the TARA Oceans eukaryotic metagenome dataset use the UAG codon to putatively encode leucine. We identified novel suppressor tRNA genes in two of these genomes which are predicted to decode the reassigned UAG codon to leucine. Phylogenomics analysis revealed that these three uncultivated taxa form a monophyletic lineage within the Phyllopharyngea class. Expanding our analysis by reassembling published phyllopharyngean genome datasets led to the discovery that the UAG codon had also been reassigned to putatively code for glutamine in Hartmannula sinica and Trochilia petrani. Phylogenomics analysis suggests that this occurred via two independent genetic code change events. These data demonstrate that the reassigned UAG codons have widespread usage as sense codons within the phyllopharyngean ciliates. Furthermore, we show that the function of UAA is firmly fixed as the preferred stop codon. These findings shed light on the evolvability of the genetic code in understudied microbial eukaryotes.
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spelling doaj-art-e013f9de9bf84437a214b42e5f582d672025-08-20T02:46:20ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042024-12-012012e101151210.1371/journal.pgen.1011512Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.Jamie McGowanThomas A RichardsNeil HallDavid SwarbreckThe translation of nucleotide sequences into amino acid sequences, governed by the genetic code, is one of the most conserved features of molecular biology. The standard genetic code, which uses 61 sense codons to encode one of the 20 standard amino acids and 3 stop codons (UAA, UAG, and UGA) to terminate translation, is used by most extant organisms. The protistan phylum Ciliophora (the 'ciliates') are the most prominent exception to this norm, exhibiting the grfeatest diversity of nuclear genetic code variants and evidence of repeated changes in the code. In this study, we report the discovery of multiple independent genetic code changes within the Phyllopharyngea class of ciliates. By mining publicly available ciliate genome datasets, we discovered that three ciliate species from the TARA Oceans eukaryotic metagenome dataset use the UAG codon to putatively encode leucine. We identified novel suppressor tRNA genes in two of these genomes which are predicted to decode the reassigned UAG codon to leucine. Phylogenomics analysis revealed that these three uncultivated taxa form a monophyletic lineage within the Phyllopharyngea class. Expanding our analysis by reassembling published phyllopharyngean genome datasets led to the discovery that the UAG codon had also been reassigned to putatively code for glutamine in Hartmannula sinica and Trochilia petrani. Phylogenomics analysis suggests that this occurred via two independent genetic code change events. These data demonstrate that the reassigned UAG codons have widespread usage as sense codons within the phyllopharyngean ciliates. Furthermore, we show that the function of UAA is firmly fixed as the preferred stop codon. These findings shed light on the evolvability of the genetic code in understudied microbial eukaryotes.https://doi.org/10.1371/journal.pgen.1011512
spellingShingle Jamie McGowan
Thomas A Richards
Neil Hall
David Swarbreck
Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.
PLoS Genetics
title Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.
title_full Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.
title_fullStr Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.
title_full_unstemmed Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.
title_short Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates.
title_sort multiple independent genetic code reassignments of the uag stop codon in phyllopharyngean ciliates
url https://doi.org/10.1371/journal.pgen.1011512
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