Maternally regulated gastrulation as a source of variation contributing to cavefish forebrain evolution

Elife. 2019 Oct 31:8:e50160. doi: 10.7554/eLife.50160.

Abstract

Sequential developmental events, starting from the moment of fertilization, are crucial for the acquisition of animal body plan. Subtle modifications in such early events are likely to have major impacts in later morphogenesis, bringing along morphological diversification. Here, comparing the blind cave and the surface morphotypes of Astyanax mexicanus fish, we found heterochronies during gastrulation that produce organizer and axial mesoderm tissues with different properties (including differences in the expression of dkk1b) that may have contributed to cavefish brain evolution. These variations observed during gastrulation depend fully on maternal factors. The developmental evolution of retinal morphogenesis and hypothalamic patterning are among those traits that retained significant maternal influence at larval stages. Transcriptomic analysis of fertilized eggs from both morphotypes and reciprocal F1 hybrids showed a strong and specific maternal signature. Our work strongly suggests that maternal effect genes and developmental heterochronies that occur during gastrulation have impacted morphological brain change during cavefish evolution.

Keywords: Astyanax mexicanus; developmental biology; developmental evolution; dkk1b; evolutionary biology; heterocrhony; maternal transcriptome; prechordal plate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Evolution*
  • Characidae / anatomy & histology
  • Characidae / embryology*
  • Characidae / physiology*
  • Embryonic Development / genetics
  • Eye / embryology
  • Female
  • Gastrula / metabolism
  • Gastrulation / physiology*
  • Gene Expression Regulation, Developmental
  • Mesoderm / embryology
  • Peptides / metabolism
  • Phenotype
  • Prosencephalon / embryology
  • Prosencephalon / physiology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • Peptides
  • RNA, Messenger

Associated data

  • SRA/PRJNA545230