Cell -size regulation in budding yeast does not depend on linear accumulation of Whi5

被引:26
作者
Barber, Felix [1 ]
Amir, Ariel [2 ]
Murray, Andrew W. [1 ,3 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[3] Harvard Univ, FAS Ctr Syst Biol, Cambridge, MA 02138 USA
基金
美国国家科学基金会;
关键词
cell-size control; budding yeast; single-cell time-lapse microscopy; Start; Whi5; SACCHAROMYCES-CEREVISIAE; GENE-EXPRESSION; G1/S TRANSCRIPTION; POSITIVE FEEDBACK; GROWTH; DIVISION; CLN3; INHIBITOR; ACTIVATOR; INITIATION;
D O I
10.1073/pnas.2001255117
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cells must couple cell-cycle progress to their growth rate to restrict the spread of cell sizes present throughout a population. Linear, rather than exponential, accumulation of Whi5, was proposed to provide this coordination by causing a higher Whi5 concentration in cells born at a smaller size. We tested this model using the inducible GAL7 promoter to make the Whi5 concentration independent of cell size. At an expression level that equalizes the mean cell size with that of wild-type cells, the size distributions of cells with galactose-induced Whi5 expression and wild-type cells are indistinguishable. Fluorescence microscopy confirms that the endogenous and GAL7 promoters produce different relationships between Whi5 concentration and cell volume without diminishing size control in the G1 phase. We also expressed Cln3 from the GAL1 promoter, finding that the spread in cell sizes for an asynchronous population is unaffected by this perturbation. Our findings indicate that size control in budding yeast does not fundamentally originate from the linear accumulation of Whi5, contradicting a previous claim and demonstrating the need for further models of cell-cycle regulation to explain how cell size controls passage through Start.
引用
收藏
页码:14243 / 14250
页数:8
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