Wang Yonggang, Nakashima Nobutaka, Sekiguchi Takeshi, Nishimoto Takeharu
Department of Molecular Biology, Graduate School of Medical Science, Kyushu University, Fukuoka 812-8582, Japan.
Biochem Biophys Res Commun. 2005 Oct 21;336(2):639-45. doi: 10.1016/j.bbrc.2005.08.108.
A Gtr1p GTPase, the GDP mutant of which suppresses both temperature-sensitive mutants of Saccharomyces cerevisiae RanGEF/Prp20p and RanGAP/Rna1p, was presently found to interact with Yrb2p, the S. cerevisiae homologue of mammalian Ran-binding protein 3. Gtr1p bound the Ran-binding domain of Yrb2p. In contrast, Gtr2p, a partner of Gtr1p, did not bind Yrb2p, although it bound Gtr1p. A triple mutant: yrb2delta gtr1delta gtr2delta was lethal, while a double mutant: gtr1delta gtr2delta survived well, indicating that Yrb2p protected cells from the killing effect of gtr1delta gtr2delta. Recombinant Gtr1p and Gtr2p were purified as a complex from Escherichia coli. The resulting Gtr1p-Gtr2p complex was comprised of an equal amount of Gtr1p and Gtr2p, which inhibited the Rna1p/Yrb2 dependent RanGAP activity. Thus, the Gtr1p-Gtr2p cycle was suggested to regulate the Ran cycle through Yrb2p.
目前发现一种Gtr1p GTP酶,其GDP突变体可抑制酿酒酵母RanGEF/Prp20p和RanGAP/Rna1p的温度敏感突变体,它能与哺乳动物Ran结合蛋白3的酿酒酵母同源物Yrb2p相互作用。Gtr1p与Yrb2p的Ran结合结构域结合。相比之下,Gtr1p的伙伴Gtr2p虽然能与Gtr1p结合,但不与Yrb2p结合。一个三突变体:yrb2δ gtr1δ gtr2δ是致死的,而双突变体:gtr1δ gtr2δ存活良好,这表明Yrb2p可保护细胞免受gtr1δ gtr2δ的杀伤作用。重组Gtr1p和Gtr2p作为复合物从大肠杆菌中纯化出来。所得的Gtr1p - Gtr2p复合物由等量的Gtr1p和Gtr2p组成,它抑制Rna1p/Yrb2依赖的RanGAP活性。因此,提示Gtr1p - Gtr2p循环通过Yrb2p调节Ran循环。