Evidence map›Paper›PMID 38807159›Full record

ArticleGenome biology2024

Reproductive isolation arises during laboratory adaptation to a novel hot environment.

Sheng-Kai Hsu, Wei-Yun Lai, Johannes Novak, Felix Lehner, Ana Marija Jakšić, Elisabetta Versace, Christian Schlötterer

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In one paragraph

Article in Genome biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Sheng-Kai HsuInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria.
Wei-Yun LaiInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria.
Johannes NovakInstitute of Animal Nutrition and Functional Plant Compounds, Vetmeduni Vienna, Vienna, Austria.
Felix LehnerInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria.
Ana Marija JakšićInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria.
Elisabetta VersaceDepartment of Biological and Experimental Psychology, Queen Mary University of London, London, UK.
Christian SchlöttererInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria. christian.schloetterer@vetmeduni.ac.at.ORCID 0000-0003-4710-6526

Funding

Austrian Science Fund W1225European Research CouncilHORIZON EUROPE European Research Council ArchAdapt
6 · The paper itself

Abstract

backgroundReproductive isolation can result from adaptive processes (e.g., ecological speciation and mutation-order speciation) or stochastic processes such as "system drift" model. Ecological speciation predicts barriers to gene flow between populations from different environments, but not among replicate populations from the same environment. In contrast, reproductive isolation among populations independently adapted to the same/similar environment can arise from both mutation-order speciation or system drift.

resultsIn experimentally evolved populations adapting to a hot environment for over 100 generations, we find evidence for pre- and postmating reproductive isolation. On one hand, an altered lipid metabolism and cuticular hydrocarbon composition pointed to possible premating barriers between the ancestral and replicate evolved populations. On the other hand, the pronounced gene expression differences in male reproductive genes may underlie the postmating isolation among replicate evolved populations adapting to the same environment with the same standing genetic variation.

conclusionOur study confirms that replicated evolution experiments provide valuable insights into the mechanisms of speciation. The rapid emergence of the premating reproductive isolation during temperature adaptation showcases incipient ecological speciation. The potential evidence of postmating reproductive isolation among replicates gave rise to two hypotheses: (1) mutation-order speciation through a common selection on early fecundity leading to an inherent inter-locus sexual conflict; (2) system drift with genetic drift along the neutral ridges.

Indexed as

Hot TemperatureReproductive IsolationAdaptation, PhysiologicalAnimalsFemaleGenetic SpeciationLipid MetabolismMaleDrosophila simulansEcological speciationExperimental evolutionMutation order speciation

Identifiers

PMID38807159
PMCPMC11134630

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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.