Mazzoni C, Zarov P, Rambourg A, Mann C
Service de Biochimie et Génétique Moléculaire, Centre d'Etudes de Saclay, Gif-sur-Yvette, France.
J Cell Biol. 1993 Dec;123(6 Pt 2):1821-33. doi: 10.1083/jcb.123.6.1821.
Bud emergence, spindle pole body duplication and DNA replication are all dependent on the activation of the CDC28 protein kinase at the Start point in the G1 phase of the cell cycle. Bud emergence requires polarization of the cytoskeleton and secretory vesicles to a specific site on the cell surface. Cdc28p activated by G1-cyclins triggers polarization of actin to the site of bud emergence and favors apical bud growth (Lew, D. J., and S. I. Reed. 1993. J. Cell Biol. 120:1305-1320). We isolated slt2-1 as a mutation that enhances the division defect of cdc28 mutants with defects at Start. Slt2p(Mpk1p) is a member of the MAP kinase family (Lee, K. S., K. Irie, Y. Gotoh, Y. Watanabe, H. Araki, E. Nishida, K. Matsumoto, and D. E. Levin. 1993. Mol. Cell. Biol. 13:3067-3075). We show that slt2 mutants exhibit phenotypes similar to those shown by mutants of the yeast actin cytoskeleton, including delocalization of chitin deposition and of actin cortical spots and the accumulation of secretory pathway membranes and vesicles. Furthermore, slt2::HIS3 act1-1 and slt2::HIS3 myo2-66 double mutants are inviable. We suggest that Slt2p functions downstream or in parallel with Cdc28p in promoting bud formation and apical growth.
芽的出现、纺锤极体复制和DNA复制都依赖于细胞周期G1期起始点处CDC28蛋白激酶的激活。芽的出现需要细胞骨架和分泌囊泡极化到细胞表面的特定部位。由G1 - 细胞周期蛋白激活的Cdc28p触发肌动蛋白向芽出现部位的极化,并有利于顶端芽的生长(Lew, D. J., and S. I. Reed. 1993. J. Cell Biol. 120:1305 - 1320)。我们分离到slt2 - 1作为一种突变,它增强了在起始点有缺陷的cdc28突变体的分裂缺陷。Slt2p(Mpk1p)是丝裂原活化蛋白激酶家族的成员(Lee, K. S., K. Irie, Y. Gotoh, Y. Watanabe, H. Araki, E. Nishida, K. Matsumoto, and D. E. Levin. 1993. Mol. Cell. Biol. 13:3067 - 3075)。我们发现slt2突变体表现出与酵母肌动蛋白细胞骨架突变体相似的表型,包括几丁质沉积和肌动蛋白皮质斑的定位异常以及分泌途径膜和囊泡的积累。此外,slt2::HIS3 act1 - 1和slt2::HIS3 myo2 - 66双突变体是不可存活的。我们认为Slt2p在促进芽形成和顶端生长中在Cdc28p的下游起作用或与之平行发挥作用。