Insights into the biological functions of Dock family guanine nucleotide exchange factors

被引:125
作者
Laurin, Melanie [1 ,2 ]
Cote, Jean-Francois [1 ,2 ,3 ,4 ]
机构
[1] Inst Rech Clin Montreal, Montreal, PQ H2W 1R7, Canada
[2] Univ Montreal, Dept Med, Programmes Biol Mol, Montreal, PQ H3T 1J4, Canada
[3] Univ Montreal, Dept Biochim, Montreal, PQ H3T 1J4, Canada
[4] McGill Univ, Dept Anat & Cell Biol, Montreal, PQ H3A 1A3, Canada
关键词
mouse models; Dock180; Elmo; neurogenesis; myoblast fusion; migration; RAC ACTIVATOR; MYOBLAST FUSION; RHO GTPASES; MEMBRANE RECRUITMENT; AXONAL OUTGROWTH; APOPTOTIC CELLS; CDC42; ACTIVATOR; BREAST-CANCER; MOUSE MODELS; PROTEINS;
D O I
10.1101/gad.236349.113
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Rho GTPases play key regulatory roles in many aspects of embryonic development, regulating processes such as differentiation, proliferation, morphogenesis, and migration. Two families of guanine nucleotide exchange factors (GEFs) found in metazoans, Dbl and Dock, are responsible for the spatiotemporal activation of Rac and Cdc42 proteins and their downstream signaling pathways. This review focuses on the emerging roles of the mammalian DOCK family in development and disease. We also discuss, when possible, how recent discoveries concerning the biological functions of these GEFs might be exploited for the development of novel therapeutic strategies.
引用
收藏
页码:533 / 547
页数:15
相关论文
共 97 条
[1]   Myoblast fusion: lessons from flies and mice [J].
Abmayr, Susan M. ;
Pavlath, Grace K. .
DEVELOPMENT, 2012, 139 (04) :641-656
[2]  
Alan Jamie K, 2013, Small GTPases, V4, P159, DOI 10.4161/sgtp.26530
[3]   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
[4]   Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia [J].
Bergmann, C ;
Zerres, K ;
Senderek, J ;
Rudnik-Schöneborn, S ;
Eggermann, T ;
Häusler, M ;
Mull, M ;
Ramaekers, VT .
BRAIN, 2003, 126 :1537-1544
[5]   Mice with mutations of Dock7 have generalized hypopigmentation and white-spotting but show normal neurological function [J].
Blasius, Amanda L. ;
Brandl, Katharina ;
Crozat, Karine ;
Xia, Yu ;
Khovananth, Kevin ;
Krebs, Philippe ;
Smart, Nora G. ;
Zampolli, Antonella ;
Ruggeri, Zaverio M. ;
Beutler, Bruce A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (08) :2706-2711
[6]   The Rho family of small GTPases: crucial regulators of skeletal myogenesis [J].
Bryan, BA ;
Li, D ;
Wu, X ;
Liu, M .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (14) :1547-1555
[7]   Rho GTPases in hematopoietic stem cell functions [J].
Cancelas, Jose A. ;
Williams, David A. .
CURRENT OPINION IN HEMATOLOGY, 2009, 16 (04) :249-254
[8]   Inhibition of Endothelial Cell Apoptosis by Netrin-1 during Angiogenesis [J].
Castets, Marie ;
Coissieux, Marie-May ;
Delloye-Bourgeois, Celine ;
Bernard, Laure ;
Delcros, Jean-Guy ;
Bernet, Agnes ;
Laudet, Vincent ;
Mehlen, Patrick .
DEVELOPMENTAL CELL, 2009, 16 (04) :614-620
[9]   Loss of Modifier of Cell Adhesion Reveals a Pathway Leading to Axonal Degeneration [J].
Chen, Qi ;
Peto, Charles A. ;
Shelton, G. Diane ;
Mizisin, Andrew ;
Sawchenko, Paul E. ;
Schubert, David .
JOURNAL OF NEUROSCIENCE, 2009, 29 (01) :118-130
[10]   Skin melanocytes: biology and development [J].
Cichorek, Miroslawa ;
Wachulska, Malgorzata ;
Stasiewicz, Aneta ;
Tyminska, Agata .
POSTEPY DERMATOLOGII I ALERGOLOGII, 2013, 30 (01) :30-41