Cloning, central nervous system expression and chromosomal mapping of the mouse PAK-1 and PAK-3 genes

被引:13
作者
Burbelo, PD [1 ]
Kozak, CA
Finegold, AA
Hall, A
Pirone, DM
机构
[1] Georgetown Univ, Med Ctr, Vincent T Lombardi Canc Res Ctr, Washington, DC 20007 USA
[2] NIAID, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
[3] NIDR, Pain & Neurosensory Mechanisms Branch, NIH, Bethesda, MD 20892 USA
[4] Univ London Univ Coll, Dept Biochem, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
关键词
Cdc42; kinase signaling; Rac; Rho GTPases;
D O I
10.1016/S0378-1119(99)00110-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Two cDNAs encoding PAK kinases were isolated from a mouse embryo library by screening with a PCR-generated probe derived from the kinase domain of a rat PAK kinase. These cDNAs, designated PAK-1 and PAK-3? encode mouse PAK kinases of 545 and 544 amino acids, respectively. Both proteins possess an N-terminal Cdc42/Rac interacting binding domain (CRIB) and a C-terminal serine/threonine kinase domain. Comparison of the two mouse PAK kinases revealed that the proteins show 87% amino acid identity. Northern analysis of a multiple mouse tissue blot with a PAK-1 probe detected a 3.0 kb transcript that was almost exclusively expressed in the brain and spinal cord compared to other tissues such as lung, liver and kidney. A similar pattern of central nervous system tissue expression of PAK-3 transcripts of 3.6 and 8 kb was also observed. Analysis of two multilocus genetic crosses localized Pak1 and Pak3 to a position on chromosome 7 and X, respectively. The high level of PAK-1 and PAK-3 kinase expression in the mouse brain and spinal cord suggests a potentially important role for these kinases in the control of the cellular architecture and/or signaling in the central nervous system. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:209 / 215
页数:7
相关论文
共 26 条
[1]   PAK3 mutation in nonsyndromic X-linked mental retardation [J].
Allen, KM ;
Gleeson, JG ;
Bagrodia, S ;
Partington, MW ;
MacMillan, JC ;
Cerione, RA ;
Mulley, JC ;
Walsh, CA .
NATURE GENETICS, 1998, 20 (01) :25-30
[2]  
BAGRODIA S, 1995, J BIOL CHEM, V270, P27995
[3]   Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation [J].
Billuart, P ;
Bienvenu, T ;
Ronce, N ;
Des Portes, V ;
Vinet, MC ;
Zemni, R ;
Roest Crollius, H ;
Carrié, A ;
Fauchereau, F ;
Cherry, M ;
Briault, S ;
Hamel, B ;
Fryns, JP ;
Beldjord, C ;
Kahn, A ;
Moraine, C ;
Chelly, J .
NATURE, 1998, 392 (6679) :923-926
[4]   A GTPase-independent mechanism of p21-activated kinase activation - Regulation by sphingosine and other biologically active lipids [J].
Bokoch, GM ;
Reilly, AM ;
Daniels, RH ;
King, CC ;
Olivera, A ;
Spiegel, S ;
Knaus, UG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (14) :8137-8144
[5]   A CONSERVED BINDING MOTIF DEFINES NUMEROUS CANDIDATE TARGET PROTEINS FOR BOTH CDC42 AND RAC GTPASES [J].
BURBELO, PD ;
DRECHSEL, D ;
HALL, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29071-29074
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   Membrane targeting of p21-activated kinase 1 (PAK1) induces neurite outgrowth from PC12 cells [J].
Daniels, RH ;
Hall, PS ;
Bokoch, GM .
EMBO JOURNAL, 1998, 17 (03) :754-764
[8]   RAC GTPASE INTERACTS WITH GAPS AND TARGET PROTEINS THROUGH MULTIPLE EFFECTOR SITES [J].
DIEKMANN, D ;
NOBES, CD ;
BURBELO, PD ;
ABO, A ;
HALL, A .
EMBO JOURNAL, 1995, 14 (21) :5297-5305
[9]  
GREEN EL, 1981, LINKAGE RECOMBINATIO, P77
[10]   THE SCANNING MODEL FOR TRANSLATION - AN UPDATE [J].
KOZAK, M .
JOURNAL OF CELL BIOLOGY, 1989, 108 (02) :229-241