Evidence map›Paper›PMID 30252986›Full record

ArticleMolecular ecology2018

The role of gene flow in rapid and repeated evolution of cave-related traits in Mexican tetra, Astyanax mexicanus.

Adam Herman, Yaniv Brandvain, James Weagley, William R Jeffery, Alex C Keene, Thomas J Y Kono, Helena Bilandžija, Richard Borowsky, Luis Espinasa, Kelly O'Quin and 9 more

Open access · greenAbstract read
In one paragraph

Article in Molecular ecology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
38.5field-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

104 citing papers in PubMed, 221 citations in OpenAlex.

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  12. Aquifer-Mediated Speciation in Cave-Adapted Fishes.Integrative organismal biology (Oxford, England) · 2026
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44 more citing papers are in PubMed but not listed here.

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

19 authors at 14 institutions in 3 countries.

Adam HermanPlant and Microbial Biology, Gortner Lab, University of Minnesota, Saint Paul, Minnesota.ORCID 0000-0001-7463-9462
Yaniv BrandvainPlant and Microbial Biology, Gortner Lab, University of Minnesota, Saint Paul, Minnesota.
James WeagleyEcology, Evolution, and Behavior, Gortner Lab, University of Minnesota, Saint Paul, Minnesota.
William R JefferyDepartment of Biology, University of Maryland, College Park, Maryland.
Alex C KeeneDepartment of Biological Sciences, Florida Atlantic University, Jupiter, Florida.
Thomas J Y KonoMinnesota Supercomputing Institute, University of Minnesota, Minneapolis, Minnesota.
Helena BilandžijaDepartment of Molecular Biology, Rudjer Boskovic Institute, Zagreb, Croatia.
Richard BorowskyDepartment of Biology, New York University, New York, New York.
Luis EspinasaSchool of Science, Marist College, Poughkeepsie, New York.
Kelly O'QuinDepartment of Biology, Centre College, Danville, Kentucky.
Claudia P Ornelas-GarcíaDepartamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México, Coyoacán, Mexico.
Masato YoshizawaDepartment of Biology, University of Hawai'i at Mānoa, Honolulu, Hawaii.
Brian CarlsonDepartment of Biology, College of Wooster, Wooster, Ohio.
Ernesto MaldonadoUnidad Académica de Sistemas Arrecifales, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Puerto Morelos, Mexico.
Joshua B GrossDepartment of Biological Sciences, University of Cincinnati, Cincinnati, Ohio.
Reed A CartwrightThe Biodesign Institute, Arizona State University, Tempe, Arizona.ORCID 0000-0002-0837-9380
Nicolas RohnerStowers Institute for Medical Research, Kansas City, Missouri.
Wesley C WarrenMcDonnell Genome Institute, Washington University, St Louis, Missouri.
Suzanne E McGaughDepartment of Molecular Biology, Rudjer Boskovic Institute, Zagreb, Croatia.ORCID 0000-0003-3163-3436
University of Minnesota · USRuđer Bošković Institute · HRUniversidad Nacional Autónoma de México · MXArizona State University · USCentre College · USCollege of Wooster · USFlorida Atlantic University · USJames S. McDonnell Foundation · USMarist College · USNew York University · USStowers Institute for Medical Research · USUniversity of Cincinnati · USUniversity of Hawaiʻi at Mānoa · USUniversity of Maryland, College Park · US

Funding

The Control of Insect Metabolism through Nutrition-based SymbiosisP20GM125508 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Alexander Culley · 2018 to 2026
$21.2M
Virtual Reality and Augmented Reality CoreP20GM103650 · NIGMS · UNIVERSITY OF NEVADA RENO · PI WEBSTER, MICHAEL A · 2012 to 2022
$20.9M
Regulation of Eye Growth and Development by the LensR01EY014619 · NEI · UNIV OF MARYLAND, COLLEGE PARK · PI JEFFERY, WILLIAM R · 2003 to 2012
$3.8M
The developmental and genetic regulators of craniofacial asymmetryR01DE025033 · NIDCR · UNIVERSITY OF CINCINNATI · PI GROSS, JOSHUA BENJAMIN · 2015 to 2019
$2.0M
Molecular Genetic Analysis of Sclera Development and DegenerationR01EY024941 · NEI · UNIV OF MARYLAND, COLLEGE PARK · PI JEFFERY, WILLIAM R · 2015 to 2019
$1.9M
Understanding complex trait architecture through population genomicsR01GM127872 · NIGMS · UNIVERSITY OF MINNESOTA · PI KEENE, ALEX C, MCGAUGH, SUZANNE · 2018 to 2021
$1.7M
Whole genome assembly resources for aquatic models of human diseaseR24OD011198 · OD · WASHINGTON UNIVERSITY · PI WARREN, WESLEY CHARLES · 2012 to 2019
$1.4M
NEI NIH HHS R01 EY014619NEI NIH HHS R01 EY024941NIDCR NIH HHS R01 DE025033NIGMS NIH HHS P20 GM103650NIGMS NIH HHS P20 GM125508NIGMS NIH HHS R01 GM127872NIH HHS R24 OD011198
6 · The paper itself

Abstract

Understanding the molecular basis of repeatedly evolved phenotypes can yield key insights into the evolutionary process. Quantifying gene flow between populations is especially important in interpreting mechanisms of repeated phenotypic evolution, and genomic analyses have revealed that admixture occurs more frequently between diverging lineages than previously thought. In this study, we resequenced 47 whole genomes of the Mexican tetra from three cave populations, two surface populations and outgroup samples. We confirmed that cave populations are polyphyletic and two Astyanax mexicanus lineages are present in our data set. The two lineages likely diverged much more recently than previous mitochondrial estimates of 5-7 mya. Divergence of cave populations from their phylogenetically closest surface population likely occurred between ~161 and 191 k generations ago. The favoured demographic model for most population pairs accounts for divergence with secondary contact and heterogeneous gene flow across the genome, and we rigorously identified gene flow among all lineages sampled. Therefore, the evolution of cave-related traits occurred more rapidly than previously thought, and trogolomorphic traits are maintained despite gene flow with surface populations. The recency of these estimated divergence events suggests that selection may drive the evolution of cave-derived traits, as opposed to disuse and drift. Finally, we show that a key trogolomorphic phenotype QTL is enriched for genomic regions with low divergence between caves, suggesting that regions important for cave phenotypes may be transferred between caves via gene flow. Our study shows that gene flow must be considered in studies of independent, repeated trait evolution.

Indexed as

Biological EvolutionCavesGene FlowGenetics, PopulationAnimalsCharacidaeMexicoModels, GeneticPhenotypePhylogenyQuantitative Trait Loci

Identifiers

PMID30252986
PMCPMC6261294
OpenAlexW2806176244

What OpenQuestion holds

Textmetadata
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Read underepoch 390

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.