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...
Main Authors: | , , , |
---|---|
Format: | Journal article |
Language: | English |
Published: |
Public Library of Science
2024
|
_version_ | 1824458739184304128 |
---|---|
author | McGowan, J Richards, TA Hall, N Swarbreck, D |
author_facet | McGowan, J Richards, TA Hall, N Swarbreck, D |
author_sort | McGowan, J |
collection | OXFORD |
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. |
first_indexed | 2025-02-19T04:30:40Z |
format | Journal article |
id | oxford-uuid:d4fabb98-434c-476b-bf70-13bfd3659ddb |
institution | University of Oxford |
language | English |
last_indexed | 2025-02-19T04:30:40Z |
publishDate | 2024 |
publisher | Public Library of Science |
record_format | dspace |
spelling | oxford-uuid:d4fabb98-434c-476b-bf70-13bfd3659ddb2024-12-31T20:19:43ZMultiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliatesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d4fabb98-434c-476b-bf70-13bfd3659ddbEnglishJisc Publications RouterPublic Library of Science2024McGowan, JRichards, TAHall, NSwarbreck, DThe 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. |
spellingShingle | McGowan, J Richards, TA Hall, N Swarbreck, D Multiple independent genetic code reassignments of the UAG stop codon in phyllopharyngean ciliates |
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 |
work_keys_str_mv | AT mcgowanj multipleindependentgeneticcodereassignmentsoftheuagstopcodoninphyllopharyngeanciliates AT richardsta multipleindependentgeneticcodereassignmentsoftheuagstopcodoninphyllopharyngeanciliates AT halln multipleindependentgeneticcodereassignmentsoftheuagstopcodoninphyllopharyngeanciliates AT swarbreckd multipleindependentgeneticcodereassignmentsoftheuagstopcodoninphyllopharyngeanciliates |