Evidence map›Paper›PMID 37194566›Full record

ArticleMolecular biology and evolution2023

Caecilian Genomes Reveal the Molecular Basis of Adaptation and Convergent Evolution of Limblessness in Snakes and Caecilians.

Vladimir Ovchinnikov, Marcela Uliano-Silva, Mark Wilkinson, Jonathan Wood, Michelle Smith, Karen Oliver, Ying Sims, James Torrance, Alexander Suh, Shane A McCarthy and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 20 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

12 authors at 5 institutions in 2 countries.

Vladimir OvchinnikovComputational and Molecular Evolutionary Biology Group, School of Life Sciences, Faculty of Medicine and Health Science, University of Nottingham, Nottingham, United Kingdom.
Marcela Uliano-SilvaTree of Life Programme, Wellcome Sanger Institute, Cambridge, United Kingdom.ORCID 0000-0001-6723-4715
Mark WilkinsonHerpetology Laboratory, The Natural History Museum, London, United Kingdom.
Jonathan WoodTree of Life Programme, Wellcome Sanger Institute, Cambridge, United Kingdom.
Michelle SmithScientific Operations, Wellcome Sanger Institute, Cambridge, United Kingdom.
Karen OliverScientific Operations, Wellcome Sanger Institute, Cambridge, United Kingdom.
Ying SimsTree of Life Programme, Wellcome Sanger Institute, Cambridge, United Kingdom.
James TorranceTree of Life Programme, Wellcome Sanger Institute, Cambridge, United Kingdom.
Alexander SuhSchool of Biological Sciences, University of East Anglia, Norwich, United Kingdom.
Shane A McCarthyTree of Life Programme, Wellcome Sanger Institute, Cambridge, United Kingdom.ORCID 0000-0002-2715-4187
Richard DurbinTree of Life Programme, Wellcome Sanger Institute, Cambridge, United Kingdom.ORCID 0000-0002-9130-1006
Mary J O'ConnellComputational and Molecular Evolutionary Biology Group, School of Life Sciences, Faculty of Medicine and Health Science, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0002-1877-1001
Wellcome Sanger Institute · GBUniversity of Cambridge · GBUniversity of Nottingham · GBNatural History Museum · GBUniversity of East Anglia · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

We present genome sequences for the caecilians Geotrypetes seraphini (3.8 Gb) and Microcaecilia unicolor (4.7 Gb), representatives of a limbless, mostly soil-dwelling amphibian clade with reduced eyes, and unique putatively chemosensory tentacles. More than 69% of both genomes are composed of repeats, with retrotransposons being the most abundant. We identify 1,150 orthogroups that are unique to caecilians and enriched for functions in olfaction and detection of chemical signals. There are 379 orthogroups with signatures of positive selection on caecilian lineages with roles in organ development and morphogenesis, sensory perception, and immunity amongst others. We discover that caecilian genomes are missing the zone of polarizing activity regulatorysequence (ZRS) enhancer of Sonic Hedgehog which is also mutated in snakes. In vivo deletions have shown ZRS is required for limb development in mice, thus, revealing a shared molecular target implicated in the independent evolution of limblessness in snakes and caecilians.

Indexed as

AmphibiansHedgehog ProteinsAcclimatizationAnimalsEvolution, MolecularGenomeMiceSnakesHedgehog ProteinsamphibiaGymnophionalimblessnessvertebrate comparative genomics

Identifiers

PMID37194566
PMCPMC10195157
OpenAlexW4376872202

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.