European Molecular Biology Laboratory (EMBL) Barcelona, Dr. Aiguader 88, 08003 Barcelona, Spain; Collaboration for joint PhD degree between EMBL and Heidelberg University, Faculty of Biosciences, Heidelberg, Germany.
European Molecular Biology Laboratory (EMBL) Barcelona, Dr. Aiguader 88, 08003 Barcelona, Spain.
Cell Stem Cell. 2023 Jul 6;30(7):938-949.e7. doi: 10.1016/j.stem.2023.05.014. Epub 2023 Jun 20.
Differential speeds in biochemical reactions have been proposed to be responsible for the differences in developmental tempo between mice and humans. However, the underlying mechanism controlling the species-specific kinetics remains to be determined. Using in vitro differentiation of pluripotent stem cells, we recapitulated the segmentation clocks of diverse mammalian species varying in body weight and taxa: marmoset, rabbit, cattle, and rhinoceros. Together with mouse and human, the segmentation clock periods of the six species did not scale with the animal body weight, but with the embryogenesis length. The biochemical kinetics of the core clock gene HES7 displayed clear scaling with the species-specific segmentation clock period. However, the cellular metabolic rates did not show an evident correlation. Instead, genes involving biochemical reactions showed an expression pattern that scales with the segmentation clock period. Altogether, our stem cell zoo uncovered general scaling laws governing species-specific developmental tempo.
生物化学反应的差异速度被认为是导致老鼠和人类发育速度不同的原因。然而,控制物种特异性动力学的潜在机制仍有待确定。通过体外分化多能干细胞,我们再现了体重和分类学不同的多种哺乳动物的分段时钟:狨猴、兔子、牛和犀牛。与老鼠和人类一起,六种物种的分段时钟周期与动物体重不成比例,而是与胚胎发生长度成比例。核心时钟基因 HES7 的生化动力学与物种特异性分段时钟周期明显相关。然而,细胞代谢率并没有明显的相关性。相反,涉及生化反应的基因表现出与分段时钟周期相关的表达模式。总的来说,我们的干细胞动物园揭示了控制物种特异性发育速度的一般缩放定律。