Evidence map›Paper›PMID 37796765›Full record

ArticlePLoS genetics2023

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

Jamie McGowan, Estelle S Kilias, Elisabet Alacid, James Lipscombe, Benjamin H Jenkins, Karim Gharbi, Gemy G Kaithakottil, Iain C Macaulay, Seanna McTaggart, Sally D Warring and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Jamie McGowanEarlham Institute, Norwich Research Park, Norwich, United Kingdom.ORCID 0000-0002-4240-5175
Estelle S KiliasDepartment of Biology, University of Oxford, Oxford, United Kingdom.
Elisabet AlacidDepartment of Biology, University of Oxford, Oxford, United Kingdom.
James LipscombeEarlham Institute, Norwich Research Park, Norwich, United Kingdom.ORCID 0000-0002-4970-0716
Benjamin H JenkinsDepartment of Biology, University of Oxford, Oxford, United Kingdom.
Karim GharbiEarlham Institute, Norwich Research Park, Norwich, United Kingdom.
Gemy G KaithakottilEarlham Institute, Norwich Research Park, Norwich, United Kingdom.ORCID 0000-0003-1360-7808
Iain C MacaulayEarlham Institute, Norwich Research Park, Norwich, United Kingdom.
Seanna McTaggartEarlham Institute, Norwich Research Park, Norwich, United Kingdom.
Sally D WarringEarlham Institute, Norwich Research Park, Norwich, United Kingdom.
Thomas A RichardsDepartment of Biology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9692-0973
Neil HallEarlham Institute, Norwich Research Park, Norwich, United Kingdom.ORCID 0000-0003-2808-0009
David SwarbreckEarlham Institute, Norwich Research Park, Norwich, United Kingdom.ORCID 0000-0002-5453-1013
Norwich Research Park · GBUniversity of Oxford · GBUniversity of East Anglia · GB

Funding

Biotechnology and Biological Sciences Research Council BB/CCG1720/1Biotechnology and Biological Sciences Research Council BBS/E/T/000PR9814Biotechnology and Biological Sciences Research Council BBS/E/T/000PR9816Wellcome Trust
6 · The paper itself

Abstract

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.

Indexed as

Amino AcidsCiliophoraAmino Acid SequenceCodon, TerminatorGenetic CodeAmino AcidsCodon, Terminator

Identifiers

PMID37796765
PMCPMC10553269
OpenAlexW4387378562

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.