Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10769610 | Biochemical and Biophysical Research Communications | 2005 | 7 Pages |
Abstract
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: yrb2Î gtr1Î gtr2Î was lethal, while a double mutant: gtr1Î gtr2Î survived well, indicating that Yrb2p protected cells from the killing effect of gtr1Î gtr2Î. 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.
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Authors
Yonggang Wang, Nobutaka Nakashima, Takeshi Sekiguchi, Takeharu Nishimoto,