Rga2 is a Rho2 GAP that regulates morphogenesis and cell integrity in S-pombe

被引:46
作者
Antonia Villar-Tajadura, M. [1 ]
Coll, Pedro M. [1 ]
Madrid, Marisa [2 ]
Cansado, Jose [2 ]
Santos, Beatriz [1 ]
Perez, Pilar [1 ]
机构
[1] Univ Salamanca, Dept Genet & Microbiol, CSIC, Inst Microbiol Bioquim, Salamanca 37007, Spain
[2] Univ Murcia, Dept Genet & Microbiol, Murcia, Spain
关键词
D O I
10.1111/j.1365-2958.2008.06447.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Schizosaccharomyces pombe Rho2 GTPase regulates alpha-D-glucan synthesis and acts upstream of Pck2 to activate the MAP kinase pathway for cell integrity. However, little is known about its regulation. Here we describe Rga2 as a Rho2 GTPase-activating protein (GAP) that regulates cell morphology. rga2(+) gene is not essential for growth but its deletion causes longer and thinner cells whereas rga2(+) overexpression causes shorter and broader cells. rga2(+) overexpression also causes abnormal accumulation of Calcofluor-stained material and cell lysis, suggesting that it also participates in cell wall integrity. Rga2 localizes to growth tips and septum region. The N-terminal region of the protein is required for its correct localization whereas the PH domain is necessary exclusively for Rga2 localization to the division area. Also, Rga2 localization depends on polarity markers and on actin polymerization. Rga2 interacts with Rho2 and possesses in vitro and in vivo GAP activity for this GTPase. Accordingly, rga2 Delta cells contain more alpha-D-glucan and therefore partially suppress the thermosensitivity of mok1-664 cells, which have a defective alpha-D-glucan synthase. Additionally, genetic interactions and biochemical analysis suggest that Rga2 regulates Rho2-Pck2 interaction and might participate in the regulation of the MAPK cell integrity pathway.
引用
收藏
页码:867 / 881
页数:15
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