Variation in Pleiotropic Hub Gene Expression Is Associated with Interspecific Differences in Head Shape and Eye Size in Drosophila

Mol Biol Evol. 2021 May 4;38(5):1924-1942. doi: 10.1093/molbev/msaa335.

Abstract

Revealing the mechanisms underlying the breathtaking morphological diversity observed in nature is a major challenge in Biology. It has been established that recurrent mutations in hotspot genes cause the repeated evolution of morphological traits, such as body pigmentation or the gain and loss of structures. To date, however, it remains elusive whether hotspot genes contribute to natural variation in the size and shape of organs. As natural variation in head morphology is pervasive in Drosophila, we studied the molecular and developmental basis of differences in compound eye size and head shape in two closely related Drosophila species. We show differences in the progression of retinal differentiation between species and we applied comparative transcriptomics and chromatin accessibility data to identify the GATA transcription factor Pannier (Pnr) as central factor associated with these differences. Although the genetic manipulation of Pnr affected multiple aspects of dorsal head development, the effect of natural variation is restricted to a subset of the phenotypic space. We present data suggesting that this developmental constraint is caused by the coevolution of expression of pnr and its cofactor u-shaped (ush). We propose that natural variation in expression or function of highly connected developmental regulators with pleiotropic functions is a major driver for morphological evolution and we discuss implications on gene regulatory network evolution. In comparison to previous findings, our data strongly suggest that evolutionary hotspots are not the only contributors to the repeated evolution of eye size and head shape in Drosophila.

Keywords: Drosophila; evolution of development; evolutionary hotspots; eye–antennal disc; gene regulatory networks; repeated evolution.

Publication types

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

MeSH terms

  • Animals
  • Biological Evolution*
  • Compound Eye, Arthropod / anatomy & histology*
  • Compound Eye, Arthropod / growth & development
  • Drosophila / anatomy & histology*
  • Drosophila / physiology
  • Drosophila Proteins / metabolism
  • Female
  • Gene Regulatory Networks
  • Genetic Pleiotropy*
  • Head / anatomy & histology
  • Larva / growth & development
  • Male
  • Species Specificity
  • Transcription Factors / metabolism
  • Transcriptome

Substances

  • Drosophila Proteins
  • Transcription Factors
  • pnr protein, Drosophila
  • ush protein, Drosophila