An early cell shape transition drives evolutionary expansion of the human forebrain

Cell. 2021 Apr 15;184(8):2084-2102.e19. doi: 10.1016/j.cell.2021.02.050. Epub 2021 Mar 24.

Abstract

The human brain has undergone rapid expansion since humans diverged from other great apes, but the mechanism of this human-specific enlargement is still unknown. Here, we use cerebral organoids derived from human, gorilla, and chimpanzee cells to study developmental mechanisms driving evolutionary brain expansion. We find that neuroepithelial differentiation is a protracted process in apes, involving a previously unrecognized transition state characterized by a change in cell shape. Furthermore, we show that human organoids are larger due to a delay in this transition, associated with differences in interkinetic nuclear migration and cell cycle length. Comparative RNA sequencing (RNA-seq) reveals differences in expression dynamics of cell morphogenesis factors, including ZEB2, a known epithelial-mesenchymal transition regulator. We show that ZEB2 promotes neuroepithelial transition, and its manipulation and downstream signaling leads to acquisition of nonhuman ape architecture in the human context and vice versa, establishing an important role for neuroepithelial cell shape in human brain expansion.

Keywords: ZEB2; brain; brain expansion; cell shape; chimpanzee; evolution; gorilla; neural stem cells; neuroepithelium; organoids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Evolution*
  • Brain / cytology*
  • Brain / metabolism
  • Cell Differentiation
  • Cell Line
  • Cell Shape / physiology*
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / metabolism
  • Epithelial-Mesenchymal Transition / genetics
  • Gene Expression
  • Gorilla gorilla
  • Humans
  • Induced Pluripotent Stem Cells / cytology
  • Induced Pluripotent Stem Cells / metabolism
  • Neurogenesis
  • Neurons / cytology
  • Neurons / metabolism
  • Organoids / cytology
  • Organoids / metabolism
  • Pan troglodytes
  • Zinc Finger E-box Binding Homeobox 2 / genetics
  • Zinc Finger E-box Binding Homeobox 2 / metabolism

Substances

  • ZEB2 protein, human
  • Zinc Finger E-box Binding Homeobox 2