Tsugawa Satoru, Hervieux Nathan, Kierzkowski Daniel, Routier-Kierzkowska Anne-Lise, Sapala Aleksandra, Hamant Olivier, Smith Richard S, Roeder Adrienne H K, Boudaoud Arezki, Li Chun-Biu
Theoretical Biology Laboratory, RIKEN, Wako 351-0198, Japan.
Laboratoire de Reproduction et Développement des Plantes, Universiteé de Lyon, ENS de Lyon, Université Claude Bernard Lyon 1, INRA, CNRS, 46 Allée d'Italie, 69364 Lyon Cedex 07, France.
Development. 2017 Dec 1;144(23):4398-4405. doi: 10.1242/dev.153999.
Organs form with remarkably consistent sizes and shapes during development, whereas a high variability in growth is observed at the cell level. Given this contrast, it is unclear how such consistency in organ scale can emerge from cellular behavior. Here, we examine an intermediate scale, the growth of clones of cells in sepals. Each clone consists of the progeny of a single progenitor cell. At early stages, we find that clones derived from a small progenitor cell grow faster than those derived from a large progenitor cell. This results in a reduction in clone size variability, a phenomenon we refer to as size uniformization. By contrast, at later stages of clone growth, clones change their growth pattern to enhance size variability, when clones derived from larger progenitor cells grow faster than those derived from smaller progenitor cells. Finally, we find that, at early stages, fast growing clones exhibit greater cell growth heterogeneity. Thus, cellular variability in growth might contribute to a decrease in the variability of clones throughout the sepal.
在发育过程中,器官形成时具有显著一致的大小和形状,而在细胞水平上观察到生长存在高度变异性。鉴于这种差异,尚不清楚器官尺度上的这种一致性是如何从细胞行为中产生的。在这里,我们研究一个中间尺度,即萼片中细胞克隆的生长。每个克隆由单个祖细胞的后代组成。在早期阶段,我们发现源自小祖细胞的克隆比源自大祖细胞的克隆生长得更快。这导致克隆大小变异性降低,我们将这种现象称为大小均匀化。相比之下,在克隆生长的后期阶段,克隆会改变其生长模式以增强大小变异性,此时源自较大祖细胞的克隆比源自较小祖细胞的克隆生长得更快。最后,我们发现,在早期阶段,快速生长的克隆表现出更大的细胞生长异质性。因此,细胞生长的变异性可能有助于降低整个萼片中克隆的变异性。