Proceedings of the National Academy of Sciences of the United States of America
Geisel School of Medicine
Ran/TC4, a Ras-like GTP-binding protein, and its nucleotide exchanger, RCC1, have been implicated in control of protein movement into the nucleus and cytoplasmic accumulation of mRNA. Saccharomyces cerevisiae contains two homologues of the mammalian Ran/TC4, encoded by the GSP1 and GSP2 genes. We have constructed yeast strains that overproduce either wild-type Gsp1 or a form of Gsp1 with glycine-21 converted to valine (Gsp1-G21V), which we show stabilizes the GTP-bound form. Cells producing Gsp1-G21V have defects in localization of nuclear proteins; nuclear proteins accumulate in the cytoplasm following galactose induction of Gsp1-G21V. Similarly, cells producing Gsp1-G21V retain poly(A)+ RNA in their nuclei. These findings suggest that hydrolysis of GTP by Ran/TC4 is necessary for proper import of proteins into the nucleus and appearance of poly(A)+ RNA in the cytoplasm.
Schlenstedt G, Saavedra C, Loeb JD, Cole CN, Silver PA. The GTP-bound form of the yeast Ran/TC4 homologue blocks nuclear protein import and appearance of poly(A)+ RNA in the cytoplasm. Proc Natl Acad Sci U S A. 1995;92(1):225-229. doi:10.1073/pnas.92.1.225
Dartmouth Digital Commons Citation
Schlenstedt, Gabriel; Saavedra, Claudio; Loeb, Jonathan D.; Cole, Charles N.; and Silver, Pamela A., "The GTP-Bound Form of the Yeast Ran/TC4 Homologue Blocks Nuclear Protein Import and Appearance of Poly(A)+ RNA in the Cytoplasm." (1995). Dartmouth Scholarship. 1637.