Evidence map›Paper›PMID 26114425›Full record

ArticlePLoS genetics2015

Reproductive Mode and the Evolution of Genome Size and Structure in Caenorhabditis Nematodes.

Janna L Fierst, John H Willis, Cristel G Thomas, Wei Wang, Rose M Reynolds, Timothy E Ahearne, Asher D Cutter, Patrick C Phillips

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 140 citations in OpenAlex.

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  5. Review
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  16. Parental-effect gene-drive elements under partial selfing, or why dobioRxiv : the preprint server for biology · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. Article

20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Janna L FierstInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, United States of America.
John H WillisInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, United States of America.
Cristel G ThomasDepartment of Ecology and Evolutionary Biology and Centre for the Analysis of Genome Evolution and Function, University of Toronto, Ontario, Canada.
Wei WangDepartment of Ecology and Evolutionary Biology and Centre for the Analysis of Genome Evolution and Function, University of Toronto, Ontario, Canada.
Rose M ReynoldsInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, United States of America.
Timothy E AhearneInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, United States of America.
Asher D CutterDepartment of Ecology and Evolutionary Biology and Centre for the Analysis of Genome Evolution and Function, University of Toronto, Ontario, Canada.
Patrick C PhillipsInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, United States of America.
University of Oregon · USUniversity of Toronto · CA

Funding

Functional and population genomics of small RNA regulationR01GM096008 · NIGMS · UNIVERSITY OF OREGON · PI CUTTER, ASHER DAMON, PHILLIPS, PATRICK C. · 2011 to 2014
$1.5M
NIGMS NIH HHS R01 GM096008NIGMS NIH HHS R01-GM096008
6 · The paper itself

Abstract

The self-fertile nematode worms Caenorhabditis elegans, C. briggsae, and C. tropicalis evolved independently from outcrossing male-female ancestors and have genomes 20-40% smaller than closely related outcrossing relatives. This pattern of smaller genomes for selfing species and larger genomes for closely related outcrossing species is also seen in plants. We use comparative genomics, including the first high quality genome assembly for an outcrossing member of the genus (C. remanei) to test several hypotheses for the evolution of genome reduction under a change in mating system. Unlike plants, it does not appear that reductions in the number of repetitive elements, such as transposable elements, are an important contributor to the change in genome size. Instead, all functional genomic categories are lost in approximately equal proportions. Theory predicts that self-fertilization should equalize the effective population size, as well as the resulting effects of genetic drift, between the X chromosome and autosomes. Contrary to this, we find that the self-fertile C. briggsae and C. elegans have larger intergenic spaces and larger protein-coding genes on the X chromosome when compared to autosomes, while C. remanei actually has smaller introns on the X chromosome than either self-reproducing species. Rather than being driven by mutational biases and/or genetic drift caused by a reduction in effective population size under self reproduction, changes in genome size in this group of nematodes appear to be caused by genome-wide patterns of gene loss, most likely generated by genomic adaptation to self reproduction per se.

Indexed as

Biological EvolutionGenome, HelminthGenome SizeAnimalsCaenorhabditisCaenorhabditis elegansDNA Transposable ElementsFemaleHelminth ProteinsMaleReproductionSelf-FertilizationX ChromosomeDNA Transposable ElementsHelminth Proteins

Identifiers

PMID26114425
PMCPMC4482642
OpenAlexW1841800506

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.