Department of Biomedical Science, University of Sheffield, Sheffield, United Kingdom.
Elife. 2019 Sep 23;8:e47625. doi: 10.7554/eLife.47625.
A fundamental question is how proliferation and growth are timed during embryogenesis. Although it has been suggested that the cell cycle could be a timer, the underlying mechanisms remain elusive. Here we describe a cell cycle timer that operates in ()-expressing polarising region cells of the chick wing bud. Our data are consistent with Shh signalling stimulating polarising region cell proliferation via Cyclin D2, and then inhibiting proliferation via a Bmp2-p27 pathway. When Shh signalling is blocked, polarising region cells over-proliferate and form an additional digit, which can be prevented by applying Bmp2 or by inhibiting D cyclin activity. In addition, Bmp2 also restores posterior digit identity in the absence of Shh signalling, thus indicating that it specifies antero-posterior (thumb to little finger) positional values. Our results reveal how an autoregulatory cell cycle timer integrates growth and specification and are widely applicable to many tissues.
一个基本的问题是胚胎发生过程中增殖和生长是如何定时的。虽然有人提出细胞周期可能是一个定时器,但潜在的机制仍难以捉摸。在这里,我们描述了一个在鸡翅膀芽表达 Shh 的极化区细胞中起作用的细胞周期定时器。我们的数据与 Shh 信号通过 Cyclin D2 刺激极化区细胞增殖,然后通过 Bmp2-p27 途径抑制增殖的观点一致。当 Shh 信号被阻断时,极化区细胞过度增殖并形成额外的指,通过应用 Bmp2 或抑制 D 周期蛋白活性可以防止这种情况发生。此外,Bmp2 还可以在没有 Shh 信号的情况下恢复后指的身份,这表明它指定了前后(拇指到小指)的位置值。我们的结果揭示了自调节细胞周期定时器如何整合生长和规范,并且广泛适用于许多组织。