A novel factor modulating X chromosome dosage compensation in Anopheles

Curr Biol. 2023 Nov 6;33(21):4697-4703.e4. doi: 10.1016/j.cub.2023.09.001. Epub 2023 Sep 28.

Abstract

Dosage compensation (DC), a process countering chromosomal imbalance in individuals with heteromorphic sex chromosomes, has been molecularly characterized only in mammals, Caenorhabditis elegans, and fruit flies.1 In Drosophila melanogaster males, it is achieved by an approximately 2-fold hypertranscription of the monosomic X chromosome mediated by the MSL complex.2,3 The complex is not assembled on female X chromosomes because production of its key protein MSL-2 is prevented due to intron retention and inhibition of translation by Sex-lethal, a female-specific protein operating at the top of the sex determination pathway.4 It remains unclear how DC is mechanistically regulated in other insects. In the malaria mosquito Anopheles gambiae, an approximately 2-fold hypertranscription of the male X also occurs5 by a yet-unknown molecular mechanism distinct from that in D. melanogaster.6 Here we show that a male-specifically spliced gene we call 007, which arose by a tandem duplication in the Anopheles ancestral lineage, is involved in the control of DC in males. Homozygous 007 knockouts lead to a global downregulation of the male X, phenotypically manifested by a slower development compared to wild-type mosquitoes or mutant females-however, without loss of viability or fertility. In females, a 007 intron retention promoted by the sex determination protein Femaleless, known to prevent hypertranscription from both X chromosomes,7 introduces a premature termination codon apparently rendering the female transcripts non-productive. In addition to providing a unique perspective on DC evolution, the 007, with its conserved properties, may represent an important addition to a genetic toolbox for malaria vector control.

Keywords: developmental delay; female-specific intron retention; gene knockout; malaria vector; male-specific splicing; tandem gene duplication.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Anopheles* / genetics
  • Drosophila / genetics
  • Drosophila Proteins* / genetics
  • Drosophila melanogaster / genetics
  • Factor X / genetics
  • Female
  • Malaria* / genetics
  • Male
  • Mammals / genetics
  • Mosquito Vectors
  • X Chromosome / genetics

Substances

  • Factor X
  • Drosophila Proteins