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Mol. Cell. Biol., Apr 1997, 2247-2256, Vol 17, No. 4
S Vincent and J Settleman
The Ras-related Rho family GTPases mediate signal transduction pathways
that regulate a variety of cellular processes. Like Ras, the Rho proteins
(which include Rho, Rac, and CDC42) interact directly with protein kinases,
which are likely to serve as downstream effector targets of the activated
GTPase. Activated RhoA has recently been reported to interact directly with
several protein kinases, p120 PKN, p150 ROK alpha and -beta, p160 ROCK, and
p164 Rho kinase. Here, we describe the purification of a novel
Rho-associated kinase, p140, which appears to be the major Rho-associated
kinase activity in most tissues. Peptide microsequencing revealed that p140
is probably identical to the previously reported PRK2 kinase, a close
relative of PKN. However, unlike the previously described Rho-binding
kinases, which are Rho specific, p140 associates with Rac as well as Rho.
Moreover, the interaction of p140 with Rho in vitro is nucleotide
independent, whereas the interaction with Rac is completely GTP dependent.
The association of p140 with either GTPase promotes kinase activity
substantially, and expression of a kinase-deficient form of p140 in
microinjected fibroblasts disrupts actin stress fibers. These results
indicate that p140 may be a shared kinase target of both Rho and Rac
GTPases that mediates their effects on rearrangements of the actin
cytoskeleton.
Copyright © 1997, American Society for Microbiology
The PRK2 kinase is a potential effector target of both Rho and Rac GTPases and regulates actin cytoskeletal organization
Massachusetts General Hospital Cancer Center and Harvard Medical School, Charlestown 02129, USA.
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