School of Life Sciences, Swiss Federal Institute of Technology in Lausanne (EPFL), CH-1015, Lausanne, Switzerland.
Adv Biosyst. 2020 Feb;4(2):e1900103. doi: 10.1002/adbi.201900103. Epub 2019 Dec 16.
Three models of division control are proposed to achieve cell size homeostasis: sizer, timer, and adder. However, few published studies of division control take into account the dynamics of single-cell growth and most assume that single-cell growth is exponential. Here, computational simulations considering exponential, linear, and bilinear growth models are performed. These simulations confirm that a timer division control model alone cannot lead to size homeostasis if the single-cell growth model is exponential. Furthermore, timer and adder division control models cannot be distinguished if the single-cell growth model is linear. Models of division control cannot be easily differentiated by analysis of average cell behavior because the birth sizes of the majority of cells are close to the population average. However, the differences between division control models are amplified in outlier cells whose birth size is far from the average. A method is introduced for vector field analysis of the speed of convergence of outlier lineages toward the steady-state birth size, which can help to distinguish between division control models and single-cell growth models.
sizer、timer 和 adder。然而,很少有关于分裂控制的已发表研究考虑到单细胞生长的动力学,并且大多数研究假设单细胞生长是指数型的。在这里,考虑了指数型、线性和双线性生长模型的计算模拟。这些模拟证实,如果单细胞生长模型是指数型的,那么仅仅依靠 timer 分裂控制模型不能实现大小的动态平衡。此外,如果单细胞生长模型是线性的,那么 timer 和 adder 分裂控制模型就无法区分。由于大多数细胞的出生大小接近群体平均值,因此通过分析细胞平均行为,很难区分分裂控制模型。然而,在出生大小远离平均值的离群细胞中,分裂控制模型之间的差异被放大了。引入了一种用于分析离群谱系向稳态出生大小收敛速度的向量场分析方法,这有助于区分分裂控制模型和单细胞生长模型。