Using a female-specific isoform of doublesex to explore male-specific hearing in mosquitoes

Animal reproduction relies on elaborate divisions of labor, and multiple dimorphisms, between the sexes. Primary dimorphisms affect core reproductive elements; secondary dimorphisms affect indirect traits, including complex behaviors. Male disease-transmitting mosquitoes locate female mating partners acoustically before copulation (phonotaxis). Male ears-and hearing performance-have thus evolved to become substantially more complex, partly due to sex-specific expression of the gene <i>doublesex</i> (<i>dsx</i>). <i>dsx</i> links primary and secondary dimorphisms: spermatogenesis and ear morphogenesis share considerable molecular overlap; both depend on <i>dsx</i> expression patterns. Here, we combine functional-anatomical analyses of mosquito ears with transcriptomic profiling to dissect <i>dsx</i>-dependent hearing in the malaria mosquito <i>Anopheles gambiae</i>. Female <i>dsx</i> mutant ears are anatomically and functionally intersex, although they still completely lack some male-specific characteristics. By cross-linking our auditory findings to the genetic bases of spermatogenesis we advance the molecular understanding of sex-specific hearing mechanisms in insects, highlighting the special roles of ciliary factors.

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Publication Details

Journal
iScience
Published
2025-08-28
DOI
https://doi.org/10.1016/j.isci.2025.113330
Citations
1
Primary Topic
Animal Behavior and Reproduction
Type
article
Field-Weighted Citation Impact
3.03

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article

Using a female-specific isoform of doublesex to explore male-specific hearing in mosquitoes

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article

Using a female-specific isoform of doublesex to explore male-specific hearing in mosquitoes

Yifeng Y. J. Xu, Marcos Georgiades, Kyros Kyrou, Andrea Crisanti, Jason Somers, YuMin M. Loh, Judit Bagi, Marta Andrés, Joerg T. Albert, Matthew P. Su
article en
1 citations

Abstract

Animal reproduction relies on elaborate divisions of labor, and multiple dimorphisms, between the sexes. Primary dimorphisms affect core reproductive elements; secondary dimorphisms affect indirect traits, including complex behaviors. Male disease-transmitting mosquitoes locate female mating partners acoustically before copulation (phonotaxis). Male ears-and hearing performance-have thus evolved to become substantially more complex, partly due to sex-specific expression of the gene <i>doublesex</i> (<i>dsx</i>). <i>dsx</i> links primary and secondary dimorphisms: spermatogenesis and ear morphogenesis share considerable molecular overlap; both depend on <i>dsx</i> expression patterns. Here, we combine functional-anatomical analyses of mosquito ears with transcriptomic profiling to dissect <i>dsx</i>-dependent hearing in the malaria mosquito <i>Anopheles gambiae</i>. Female <i>dsx</i> mutant ears are anatomically and functionally intersex, although they still completely lack some male-specific characteristics. By cross-linking our auditory findings to the genetic bases of spermatogenesis we advance the molecular understanding of sex-specific hearing mechanisms in insects, highlighting the special roles of ciliary factors.

iScienceVol. 28(9)
University of Padua (IT), The Francis Crick Institute (GB), Nagoya University Hospital (JP), National Research Council (LK), Hearing4all (DE), University College London (GB), Imperial College London (GB), Nagoya University (JP)
Imperial College London, European Commission, Ministry of Education, Culture, Sports, Science and Technology, Directorate for Biological Sciences, Horizon 2020 Framework Programme, Biotechnology and Biological Sciences Research Council, Japan Society for the Promotion of Science
Gender equality
Openalex Percentile: Top 8%
Animal Behavior and Reproduction
3.03
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