Evidence map›Paper›PMID 33988699›Full record

ArticleGenome biology and evolution2021

Molecular Evolution of Ecological Specialisation: Genomic Insights from the Diversification of Murine Rodents.

Emily Roycroft, Anang Achmadi, Colin M Callahan, Jacob A Esselstyn, Jeffrey M Good, Adnan Moussalli, Kevin C Rowe

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

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  11. Museum genomics reveals the rapid decline and extinction of Australian rodents since European settlement.Proceedings of the National Academy of Sciences of the United States of America · 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

7 authors at 5 institutions in 3 countries.

Emily RoycroftSchool of BioSciences, The University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0003-0956-5633
Anang AchmadiMuseum Zoologicum Bogoriense, Research Center for Biology, Cibinong, Jawa Barat, Indonesia.
Colin M CallahanDivision of Biological Sciences, University of Montana, Missoula, Montana, USA.
Jacob A EsselstynMuseum of Natural Science, Louisiana State University, Baton Rouge, Louisiana, USA.
Jeffrey M GoodDivision of Biological Sciences, University of Montana, Missoula, Montana, USA.
Adnan MoussalliSchool of BioSciences, The University of Melbourne, Parkville, Victoria, Australia.
Kevin C RoweSchool of BioSciences, The University of Melbourne, Parkville, Victoria, Australia.
The University of Melbourne · AUUniversity of Montana · USAustralian National University · AUIndonesian Institute of Sciences · IDLouisiana State University · US

Funding

Meiotic sex chromosome inactivation and the developmental basis of hybrid male stR01HD073439 · NICHD · UNIVERSITY OF MONTANA · PI GOOD, JEFFREY · 2012 to 2016
$1.5M
The evolution of genomic imprintingR01HD094787 · NICHD · UNIVERSITY OF MONTANA · PI GOOD, JEFFREY · 2018 to 2022
$1.5M
NICHD NIH HHS R01 HD073439NICHD NIH HHS R01 HD094787
6 · The paper itself

Abstract

Adaptive radiations are characterized by the diversification and ecological differentiation of species, and replicated cases of this process provide natural experiments for understanding the repeatability and pace of molecular evolution. During adaptive radiation, genes related to ecological specialization may be subject to recurrent positive directional selection. However, it is not clear to what extent patterns of lineage-specific ecological specialization (including phenotypic convergence) are correlated with shared signatures of molecular evolution. To test this, we sequenced whole exomes from a phylogenetically dispersed sample of 38 murine rodent species, a group characterized by multiple, nested adaptive radiations comprising extensive ecological and phenotypic diversity. We found that genes associated with immunity, reproduction, diet, digestion, and taste have been subject to pervasive positive selection during the diversification of murine rodents. We also found a significant correlation between genome-wide positive selection and dietary specialization, with a higher proportion of positively selected codon sites in derived dietary forms (i.e., carnivores and herbivores) than in ancestral forms (i.e., omnivores). Despite striking convergent evolution of skull morphology and dentition in two distantly related worm-eating specialists, we did not detect more genes with shared signatures of positive or relaxed selection than in a nonconvergent species comparison. Although a small number of the genes we detected can be incidentally linked to craniofacial morphology or diet, protein-coding regions are unlikely to be the primary genetic basis of this complex convergent phenotype. Our results suggest a link between positive selection and derived ecological phenotypes, and highlight specific genes and general functional categories that may have played an integral role in the extensive and rapid diversification of murine rodents.

Indexed as

CarnivoraRodentiaAnimalsBiological EvolutionEvolution, MolecularGenomeGenomicsMicePhylogenyadaptive radiationcomparative genomicsconvergent evolutionexome captureMurinaepositive selection

Identifiers

PMID33988699
PMCPMC8258016
OpenAlexW3162148509

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.