Evidence map›Paper›PMID 29689044›Full record

ArticlePLoS biology2018

Comparative genomics of bdelloid rotifers: Insights from desiccating and nondesiccating species.

Reuben W Nowell, Pedro Almeida, Christopher G Wilson, Thomas P Smith, Diego Fontaneto, Alastair Crisp, Gos Micklem, Alan Tunnacliffe, Chiara Boschetti, Timothy G Barraclough

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 125 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Reuben W NowellDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berkshire, United Kingdom.ORCID 0000-0001-7546-6495
Pedro AlmeidaDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berkshire, United Kingdom.
Christopher G WilsonDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berkshire, United Kingdom.
Thomas P SmithDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berkshire, United Kingdom.
Diego FontanetoNational Research Council of Italy, Institute of Ecosystem Study, Verbania Pallanza, Italy.
Alastair CrispDepartment of Chemical Engineering and Biotechnology, West Cambridge Site, University of Cambridge, Cambridge, United Kingdom.
Gos MicklemDepartment of Genetics, Cambridge Systems Biology Centre, Downing Site, University of Cambridge, Cambridge, United Kingdom.
Alan TunnacliffeDepartment of Chemical Engineering and Biotechnology, West Cambridge Site, University of Cambridge, Cambridge, United Kingdom.
Chiara BoschettiDepartment of Chemical Engineering and Biotechnology, West Cambridge Site, University of Cambridge, Cambridge, United Kingdom.
Timothy G BarracloughDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berkshire, United Kingdom.
Imperial College London · GBUniversity of Cambridge · GBInstitute of Ecosystem Study · IT

Funding

Biotechnology and Biological Sciences Research Council BB/F020562/1Biotechnology and Biological Sciences Research Council BB/F020856/1
6 · The paper itself

Abstract

Bdelloid rotifers are a class of microscopic invertebrates that have existed for millions of years apparently without sex or meiosis. They inhabit a variety of temporary and permanent freshwater habitats globally, and many species are remarkably tolerant of desiccation. Bdelloids offer an opportunity to better understand the evolution of sex and recombination, but previous work has emphasised desiccation as the cause of several unusual genomic features in this group. Here, we present high-quality whole-genome sequences of 3 bdelloid species: Rotaria macrura and R. magnacalcarata, which are both desiccation intolerant, and Adineta ricciae, which is desiccation tolerant. In combination with the published assembly of A. vaga, which is also desiccation tolerant, we apply a comparative genomics approach to evaluate the potential effects of desiccation tolerance and asexuality on genome evolution in bdelloids. We find that ancestral tetraploidy is conserved among all 4 bdelloid species, but homologous divergence in obligately aquatic Rotaria genomes is unexpectedly low. This finding is contrary to current models regarding the role of desiccation in shaping bdelloid genomes. In addition, we find that homologous regions in A. ricciae are largely collinear and do not form palindromic repeats as observed in the published A. vaga assembly. Consequently, several features interpreted as genomic evidence for long-term ameiotic evolution are not general to all bdelloid species, even within the same genus. Finally, we substantiate previous findings of high levels of horizontally transferred nonmetazoan genes in both desiccating and nondesiccating bdelloid species and show that this unusual feature is not shared by other animal phyla, even those with desiccation-tolerant representatives. These comparisons call into question the proposed role of desiccation in mediating horizontal genetic transfer.

Indexed as

Genetic SpeciationGenome, HelminthSyntenyAdaptation, PhysiologicalAnimalsDesiccationEcosystemFresh WaterGene Transfer, HorizontalGenomicsPhylogenyRotiferaTetraploidyWhole Genome Sequencing

Identifiers

PMID29689044
PMCPMC5916493
OpenAlexW2799948067

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.