Evidence using a green fluorescent protein-glucocorticoid receptor chimera that the RAN/TC4 GTPase mediates an essential function independent of nuclear protein import

被引:133
作者
Carey, KL
Richards, SA
Lounsbury, KM
Macara, IG
机构
[1] UNIV VERMONT, COLL MED, DEPT PATHOL, BURLINGTON, VT 05405 USA
[2] UNIV VERMONT, DEPT MICROBIOL MOLEC GENET, BURLINGTON, VT 05405 USA
关键词
D O I
10.1083/jcb.133.5.985
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Ran/TC4 GTPase is required for the nuclear accumulation of artificial karyophiles in permeabilized cell assays, To investigate Ran function in a physiologically intact setting using mammalian cells, we examined the effects of several Ran mutants on cell growth and on the nuclear translocation of a glucocorticoid receptor-green fluorescent protein fusion (GR-GFP). Glucocorticoid receptor is cytosolic in the absence of ligand, but translocates to the nucleus on binding the agonist dexamethasone. After transfection into baby hamster kidney cells (BHK21), GR-GFP was detectable in living cells by direct fluorescence microscopy. Addition of dexamethasone caused a rapid translocation of the chimeric protein from the cytosol into the nucleus (t(1/2) similar to 5 min), Cotransfection with epitope-tagged, wild-type Ran led to expression of HA1-Ran aa that was similar to 1.6-fold higher than the level of the endogenous protein, but it had no deleterious effect on nuclear import of the GR-GFP, However, expression of the Ran mutants G19V, T24N, or a COOH-terminal deletion (Delta C) mutant dramatically reduced the accumulation of GR-GFP in the nuclei, An L43E mutant of Ran was without significant effect on nuclear GR-GFP import. Identical results were obtained following microinjection of recombinant Ran mutants into cells expressing GR-GFP. Significantly, all of the Ran mutants, including L43E, strongly inhibited cell growth. These results demonstrate the use of GR-GFP in real-time imaging of nuclear transport. They also show that multiple types of Ran mutant exert dominant effects on this process, and that normal Ran function requires cycling between the GTP- and GDP-bound states of the protein. Most importantly, the results with the L43E Ran mutant provide strong evidence that Ran mediates a function essential to cell viability that is independent of nuclear protein import.
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页码:985 / 996
页数:12
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