Rapid evolution of female-biased genes among four species of Anopheles malaria mosquitoes

  1. Philippos A Papathanos1,6
  1. 1 University of Perugia;
  2. 2 Imperial College London;
  3. 3 University of Geneva Medical School and Swiss Institute of Bioinformatics; MIT;
  4. 4 University of Perugia and PoloGGB;
  5. 5 Welcome Trust Sanger Institute
  • * Corresponding author; email: p.papathanos{at}gmail.com
  • Abstract

    Understanding how phenotypic differences between males and females arise from the sex-biased expression of nearly identical genomes can reveal important insights into the biology and evolution of a species. Among Anopheles mosquito species, these phenotypic differences include vectorial capacity, as it is only females that blood feed and thus transmit human malaria. Here, we use RNA-seq data from multiple tissues of four vector species spanning the Anopheles phylogeny to explore the genomic and evolutionary properties of sex-biased genes. We find that in these mosquitoes, in contrast to what has been found in many other organisms, female-biased genes are more rapidly evolving in sequence, expression, and genic turnover, than male-biased genes. Our results suggest that this atypical pattern may be due to the combination of sex-specific life history challenges encountered by females, such as blood feeding. Furthermore, female propensity to mate only once in nature in male swarms likely diminishes sexual selection of post-reproductive traits related to sperm competition among males. We also develop a comparative framework to systematically explore tissue- and sex-specific splicing, to document its conservation throughout the genus and identify a set of candidate genes for future functional analyses of sex-specific isoform usage. Finally, our data reveals that the deficit of male-biased genes on the X chromosomes in Anopheles is a conserved feature in this genus and can be directly attributed to chromosome-wide transcriptional regulation that demasculinizes the X in male reproductive tissues.

    • Received October 17, 2016.
    • Accepted July 18, 2017.

    This manuscript is Open Access.

    This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International license), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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    1. Genome Res. gr.217216.116 Published by Cold Spring Harbor Laboratory Press

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