Institute of Functional Epigenetics, Helmholtz Zentrum München, 85764, Neuherberg, Germany.
German Center for Diabetes Research (DZD), 85764, Neuherberg, Germany.
Nat Commun. 2020 Jun 11;11(1):2952. doi: 10.1038/s41467-020-16764-x.
The formation and maintenance of subcellular structures and organelles with a well-defined size is a key requirement for cell function, yet our understanding of the underlying size control mechanisms is limited. While budding yeast cell polarization and subsequent assembly of a septin ring at the site of bud formation has been successfully used as a model for biological self-assembly processes, the mechanisms that set the size of the septin ring at the bud neck are unknown. Here, we use live-cell imaging and genetic manipulation of cell volume to show that the septin ring diameter increases with cell volume. This cell-volume-dependence largely accounts for modulations of ring size due to changes in ploidy and genetic manipulation of cell polarization. Our findings suggest that the ring diameter is set through the dynamic interplay of septin recruitment and Cdc42 polarization, establishing it as a model for size homeostasis of self-assembling organelles.
亚细胞结构和细胞器的形成和维持是细胞功能的关键要求,但我们对潜在的大小控制机制的理解有限。虽然出芽酵母细胞的极化和随后在芽形成部位装配一个隔膜环已被成功地用作生物自组装过程的模型,但在芽颈处设置隔膜环大小的机制尚不清楚。在这里,我们使用活细胞成像和细胞体积的遗传操作来显示隔膜环的直径随细胞体积的增加而增加。这种细胞体积依赖性在很大程度上解释了由于倍性变化和细胞极化的遗传操作引起的环大小的调制。我们的发现表明,环的直径是通过隔膜募集和 Cdc42 极化的动态相互作用来设定的,这为自组装细胞器的大小动态平衡建立了一个模型。