Department of Fundamental Microbiology, Faculty of Biology and Medicine, University of Lausanne, Biophore Building, CH-1015 Lausanne, Switzerland.
Sci Signal. 2012 Dec 4;5(253):pe53. doi: 10.1126/scisignal.2003630.
A fundamental problem in cell biology is how cells define one or several discrete sites of polarity. Through mechanisms involving positive and negative feedback, the small Rho-family guanosine triphosphatase Cdc42 breaks symmetry in round budding yeast cells to define a single site of polarized cell growth. However, it is not clear how cells can define multiple sites of polarization concurrently. We discuss a study in which rod-shaped fission yeast cells, which naturally polarize growth at their two cell ends, exhibited oscillations of Cdc42 activity between these sites. We compare these findings with similar oscillatory behavior of Cdc42 detected in budding yeast cells and discuss the possible mechanism and functional outputs of these oscillations.
细胞生物学的一个基本问题是细胞如何定义一个或多个离散的极性位点。通过涉及正反馈和负反馈的机制,小的 Rho 家族鸟苷三磷酸酶 Cdc42 在圆形出芽酵母细胞中打破对称,以定义单一的极化细胞生长位点。然而,目前尚不清楚细胞如何能够同时定义多个极化位点。我们讨论了一项研究,该研究表明,天然在其两个细胞端极化生长的杆状裂殖酵母细胞在这些位点之间表现出 Cdc42 活性的振荡。我们将这些发现与在出芽酵母细胞中检测到的类似的 Cdc42 振荡行为进行比较,并讨论这些振荡的可能机制和功能输出。