Species-specific segmentation clock periods are due to differential biochemical reaction speeds

Science. 2020 Sep 18;369(6510):1450-1455. doi: 10.1126/science.aba7668.

Abstract

Although mechanisms of embryonic development are similar between mice and humans, the time scale is generally slower in humans. To investigate these interspecies differences in development, we recapitulate murine and human segmentation clocks that display 2- to 3-hour and 5- to 6-hour oscillation periods, respectively. Our interspecies genome-swapping analyses indicate that the period difference is not due to sequence differences in the HES7 locus, the core gene of the segmentation clock. Instead, we demonstrate that multiple biochemical reactions of HES7, including the degradation and expression delays, are slower in human cells than they are in mouse cells. With the measured biochemical parameters, our mathematical model accounts for the two- to threefold period difference between the species. We propose that cell-autonomous differences in biochemical reaction speeds underlie temporal differences in development between species.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Biological Clocks / genetics*
  • Cells, Cultured
  • Embryonic Development / genetics*
  • Genetic Loci
  • Humans
  • Mesoderm / cytology
  • Mesoderm / embryology
  • Mesoderm / metabolism
  • Mice
  • Proteolysis*
  • Species Specificity
  • Time Factors

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • HES7 protein, human
  • Hes7 protein, mouse