Evidence map›Paper›PMID 26281847›Full record

ArticleBMC evolutionary biology2015

Positive selection in development and growth rate regulation genes involved in species divergence of the genus Radix.

Barbara Feldmeyer, Bastian Greshake, Elisabeth Funke, Ingo Ebersberger, Markus Pfenninger

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Article in BMC evolutionary biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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  5. Mitochondrial genome ofCurrent research in parasitology & vector-borne diseases · 2021
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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

5 authors.

Barbara FeldmeyerMolecular Ecology Group, Senckenberg Biodiversity and Climate Research Centre (BiK-F), Georg-Voigt-Str. 14-16, Frankfurt am Main, 60325, Germany. barbara.feldmeyer@senckenberg.de.
Bastian GreshakeMolecular Ecology Group, Senckenberg Biodiversity and Climate Research Centre (BiK-F), Georg-Voigt-Str. 14-16, Frankfurt am Main, 60325, Germany. greshake@bio.uni-frankfurt.de.
Elisabeth FunkeMolecular Ecology Group, Senckenberg Biodiversity and Climate Research Centre (BiK-F), Georg-Voigt-Str. 14-16, Frankfurt am Main, 60325, Germany. elifunke@gmx.de.
Ingo EbersbergerApplied Bioinformatics Group, Institute of Cell Biology and Neuroscience, Goethe University Frankfurt, Maxvon-Laue Str. 13, Frankfurt am Main, 60438, Germany. ebersberger@bio.uni-frankfurt.de.
Markus PfenningerMolecular Ecology Group, Senckenberg Biodiversity and Climate Research Centre (BiK-F), Georg-Voigt-Str. 14-16, Frankfurt am Main, 60325, Germany. Pfenninger@bio.uni-frankfurt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLife history traits like developmental time, age and size at maturity are directly related to fitness in all organisms and play a major role in adaptive evolution and speciation processes. Comparative genomic or transcriptomic approaches to identify positively selected genes involved in species divergence can help to generate hypotheses on the driving forces behind speciation. Here we use a bottom-up approach to investigate this hypothesis by comparative analysis of orthologous transcripts of four closely related European Radix species.

resultsSnails of the genus Radix occupy species specific distribution ranges with distinct climatic niches, indicating a potential for natural selection driven speciation based on ecological niche differentiation. We then inferred phylogenetic relationships among the four Radix species based on whole mt-genomes plus 23 nuclear loci. Three different tests to infer selection and changes in amino acid properties yielded a total of 134 genes with signatures of positive selection. The majority of these genes belonged to the functional gene ontology categories "reproduction" and "genitalia" with an overrepresentation of the functions "development" and "growth rate".

conclusionsWe show here that Radix species divergence may be primarily enforced by selection on life history traits such as (larval-) development and growth rate. We thus hypothesise that life history differences may confer advantages under the according climate regimes, e.g., species occupying warmer and dryer habitats might have a fitness advantage with fast developing susceptible life stages, which are more tolerant to habitat desiccation.

Indexed as

Selection, GeneticAnimalsBiological EvolutionClimateEcosystemEuropeGene Expression ProfilingGene Expression RegulationPhylogenySnailsSpecies Specificity

Identifiers

PMID26281847
PMCPMC4539673

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LicenceCC BY
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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.