Gene and Allele-Specific Expression Underlying the Electric Signal Divergence in African Weakly Electric Fish

Feng Cheng, Alice B. Dennis, Otto Baumann, Frank Kirschbaum, Salim Abdelilah-Seyfried, Ralph Tiedemann

Résultats de recherche: Contribution à un journal/une revueArticleRevue par des pairs

Résumé

In the African weakly electric fish genus Campylomormyrus, electric organ discharge signals are strikingly different in shape and duration among closely related species, contribute to prezygotic isolation, and may have triggered an adaptive radiation. We performed mRNA sequencing on electric organs and skeletal muscles (from which the electric organs derive) from 3 species with short (0.4 ms), medium (5 ms), and long (40 ms) electric organ discharges and 2 different cross-species hybrids. We identified 1,444 upregulated genes in electric organ shared by all 5 species/hybrid cohorts, rendering them candidate genes for electric organ–specific properties in Campylomormyrus. We further identified several candidate genes, including KCNJ2 and KLF5, and their upregulation may contribute to increased electric organ discharge duration. Hybrids between a short (Campylomormyrus compressirostris) and a long (Campylomormyrus rhynchophorus) discharging species exhibit electric organ discharges of intermediate duration and showed imbalanced expression of KCNJ2 alleles, pointing toward a cis-regulatory difference at this locus, relative to electric organ discharge duration. KLF5 is a transcription factor potentially balancing potassium channel gene expression, a crucial process for the formation of an electric organ discharge. Unraveling the genetic basis of the species-specific modulation of the electric organ discharge in Campylomormyrus is crucial for understanding the adaptive radiation of this emerging model taxon of ecological (perhaps even sympatric) speciation.

langue originaleAnglais
Numéro d'articlemsae021
journalMolecular biology and evolution
Volume41
Numéro de publication2
Les DOIs
Etat de la publicationPublié - 1 févr. 2024
Modification externeOui

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