Matsuda N, Ueda T, Sasaki Y, Nakano A
Molecular Membrane Biology Laboratory, RIKEN, Wako, Saitama, Japan.
Cell Struct Funct. 2000 Feb;25(1):11-20. doi: 10.1247/csf.25.11.
A large number of Rab/Ypt-family small GTPases have been identified from higher plants. While some of them can complement yeast ypt mutants, the expression of Arabidopsis Ara4 protein aggravated the growth defect of a subset of ypt mutants, probably because of the titration of common regulator(s) of yeast Ypt proteins [Ueda, T. et al. (1996) Plant Cell, 8: 2079-20911. PRA2 from pea Pisum sativum encodes an interesting Rab GTPase whose expression is regulated by light [Yoshida, K. et al. (1993) Proc. Natl. Acad. Sci. USA, 90: 6636-6640]. We examined whether PRA2 complements any of the yeast ypt mutants and found again that PRA2 does not complement but rather confers the growth defect to some of the ypt mutants. No growth defect was observed when PRA2 was expressed in the wild-type yeast cells. Unlike the case of Ara4, neither Arabidopsis nor yeast GDI remedied the growth defect by Pra2, indicating that the mechanism of the exacerbation is different. Mutational analysis of PRA2 suggests that the growth inhibition can be ascribed to unidentified factor(s) which prefers the GTP-bound form of Pra2. This yeast system will be useful for identifying such putative regulatory factor(s) from yeast and plants and analyzing their interactions with Pra2.
从高等植物中已鉴定出大量Rab/Ypt家族的小GTP酶。虽然其中一些可以互补酵母ypt突变体,但拟南芥Ara4蛋白的表达却加剧了一部分ypt突变体的生长缺陷,这可能是由于酵母Ypt蛋白的共同调节因子被滴定所致[上田,T.等人(1996年),《植物细胞》,8:2079 - 2091]。豌豆(Pisum sativum)的PRA2编码一种有趣的Rab GTP酶,其表达受光调节[吉田,K.等人(1993年),《美国国家科学院院刊》,90:6636 - 6640]。我们研究了PRA2是否能互补任何酵母ypt突变体,结果再次发现PRA2不能互补,反而会使一些ypt突变体出现生长缺陷。当PRA2在野生型酵母细胞中表达时,未观察到生长缺陷。与Ara4的情况不同,拟南芥和酵母的GDP解离抑制因子(GDI)都不能纠正Pra2导致的生长缺陷,这表明加剧生长缺陷的机制不同。对PRA2的突变分析表明,生长抑制可归因于未知因子,这些因子更倾向于Pra2的GTP结合形式。这个酵母系统将有助于从酵母和植物中鉴定此类假定的调节因子,并分析它们与Pra2的相互作用。