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(Received for publication, April 30, 1996, and in revised form, September 24, 1996)
From the Department of Pathology and Comprehensive Cancer Center,
University of Vermont, Burlington, Vermont 05405
Ran, a member of the Ras superfamily of GTPases,
is predominantly localized in the nucleus and is a necessary component
in the active transport of proteins through nuclear pores. Disruption of Ran function affects the regulation of mitosis, DNA synthesis, and
RNA processing and export. To explore the mechanisms of Ran function,
mutants of the Ran GTPase were characterized, several of which are
capable of dominantly interfering with nuclear protein import. Unlike
wild-type Ran, the putative gain-of-function mutant (G19V Ran) was not
sensitive to the exchange factor, RCC1. In addition the G19V Ran and
effector domain mutants (L43E and E46G Ran) were not sensitive to the
GTPase-activating protein, Fug1. Epitope-tagged G19V Ran and L43E Ran
isolated from transfected BHK21 cells were each about 50% GTP-bound,
whereas the wild-type and a C-terminal deletion mutant (
Volume 271, Number 51,
Issue of December 20, 1996
pp. 32834-32841
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
EFFECTS ON REGULATORY FACTOR INTERACTIONS AND SUBCELLULAR
LOCALIZATION
-DE Ran)
were primarily bound to GDP. While G19V Ran interacted with known
Ran-binding proteins and with an isolated Ran-binding domain, the T24N
Ran did not, and binding by L43E Ran was substantially reduced.
Wild-type HA1-tagged Ran expressed in BHK21 cells was nuclear, whereas
the G19V, T24N, L43E, and E46G forms of Ran were predominantly
localized at the nuclear envelope, and
-DE Ran was primarily
cytosolic. Similar results were observed when permeabilized BHK21 cells
were incubated with extracts of COS cells expressing the mutants. Thus
mutations that affect the interaction of Ran with regulatory proteins
and effectors can disrupt the normal subcellular localization of Ran, lending support for the current model of Ran-mediated nuclear import.
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