Species-specific pace of development is associated with differences in protein stability

Author:

Rayon Teresa1ORCID,Stamataki Despina1,Perez-Carrasco Ruben123,Garcia-Perez Lorena1ORCID,Barrington Christopher1ORCID,Melchionda Manuela1ORCID,Exelby Katherine1ORCID,Lazaro Jorge1ORCID,Tybulewicz Victor L. J.14ORCID,Fisher Elizabeth M. C.5ORCID,Briscoe James1ORCID

Affiliation:

1. The Francis Crick Institute, London NW1 1AT, UK.

2. Department of Mathematics, University College London, London WC1E 6BT, UK.

3. Department of Life Sciences, Imperial College London, London SW7 2AZ, UK.

4. Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

5. UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.

Abstract

Setting the tempo for development Many animals display similarities in their organization (body axis, organ systems, and so on). However, they can display vastly different life spans and thus must accommodate different developmental time scales. Two studies now compare human and mouse development (see the Perspective by Iwata and Vanderhaeghen). Matsuda et al. studied the mechanism by which the human segmentation clock displays an oscillation period of 5 to 6 hours, whereas the mouse period is 2 to 3 hours. They found that biochemical reactions, including protein degradation and delays in gene expression processes, were slower in human cells compared with their mouse counterparts. Rayon et al. looked at the developmental tempo of mouse and human embryonic stem cells as they differentiate to motor neurons in vitro. Neither the sensitivity of cells to signals nor the sequence of gene-regulatory elements could explain the differing pace of differentiation. Instead, a twofold increase in protein stability and cell cycle duration in human cells compared with mouse cells was correlated with the twofold slower rate of human differentiation. These studies show that global biochemical rates play a major role in setting the pace of development. Science , this issue p. 1450 , p. eaba7667 ; see also p. 1431

Funder

Wellcome

H2020 European Research Council

Medical Research Council

Cancer Research UK

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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