Glucose modulation of cell size in yeast. (1st February 2005)

• Record Type: Journal Article
• Authors: Vanoni, M.; Rossi, R.L.; Querin, L.; Zinzalla, V.; Alberghina, L.
• Is Part Of: Biochemical Society transactions. Volume 33:Number 1(2005)
• Page Start: 294
• Page End: 296
• Publication Date: 2005-02-01
• Subjects: cell cycle -- cell size -- Far1 -- glucose -- Gpa2 -- Gpr1 -- Sic1 -- yeast; Biochemistry -- Congresses; 572
• DOI: 10.1042/BST0330294
• Languages: English
• ISSNs: 0300-5127

Abstract

Abstract : Saccharomyces cerevisiae cells grown in glucose have larger average size than cells grown in ethanol. Besides, yeast must reach a carbon source-modulated critical cell size in order to enter S phase at Start. This control is of outmost physiological relevance, since it allows us to coordinate cell growth with cell cycle progression and it is responsible for cell size homeostasis. The cell sizer mechanism requires the overcoming of two sequential thresholds, involving Cln3 and Far1, and Clb5, 6 and Sic1, respectively. When both thresholds are non-functional, carbon source modulation of cell size at Start is completely abolished. Since inactivation of extracellular glucose sensing through deletion of either the GPR1 or the GPA2 gene causes a marked, but partial, reduction in the ability to modulate cell size and protein content at Start, it is proposed that both extracellular and intracellular glucose signalling is required for properly setting the cell sizer in glucose media.