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Blood, 1 September 2002, Vol. 100, No. 5, pp. 1679-1688
HEMATOPOIESIS
The TRQQKRP motif located near the C-terminus of Rac2 is
essential for Rac2 biologic functions and intracellular
localization
Wen Tao,
Marie-Dominique Filippi,
Jeffrey R. Bailey,
Simon J. Atkinson,
Bret Connors,
Andrew Evan, and
David A. Williams
From Howard Hughes Medical Institute;
Herman B Wells Center for Pediatric Research, Department of Pediatrics,
Department of Medicine, and Department of Anatomy, Indiana University
School of Medicine, Indianapolis, IN; and Division of Experimental
Hematology, Children's Hospital Research Foundation, Cincinnati, OH.
Rac GTPases regulate a wide variety of cellular processes
including actin cytoskeleton organization, gene expression, cell-cycle progression, and apoptosis. Here we report that the TRQQKRP
motif of Rac2 located near the C-terminus, a region of sequence
disparity among Rac proteins, is essential for complementation of Rac2
function in Rac2-deficient cells. Deletion of this sequence can also
intragenically suppress the dominant-negative Rac2D57N
mutation in a variety of functional assays. In Rac2-deficient cells, expression of TRQQKRP-deleted Rac2 protein is unable to completely rescue migration and nicotinamide adenine dinucleotide phosphate oxidase deficiencies previously described in these
cells. In fibroblasts, the Rac2D57N mutant phenotypes of
abnormal proliferation, cell morphology, and membrane ruffling are
suppressed by the TRQQKRP motif deletion. In myeloid hematopoietic
cells, the deletion of the TRQQKRP motif eliminates a
Rac2D57N-induced block in in vitro differentiation of
neutrophils not previously described with this mutant. Mechanistically,
deletion of the TRQQKRP motif results in diminished geranylgeranylation and delocalization of intracellular Rac2 protein. Taken together, these
results indicate that the TRQQKRP motif in Rac2 protein is required for
efficient prenylation and correct intracellular localization of Rac2
protein and is essential for Rac2 to mediate a variety of its biologic
functions. These data suggest that precise localization of Rac2 protein
in intracellular compartments and/or with other proteins/lipids is a
prerequisite for its diverse functions.

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