GAP control: regulating the regulators of small GTPases

被引:273
作者
Bernards, A
Settleman, J
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tcb.2004.05.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The small GTPases of the Ras superfamily mediate numerous biological processes through their ability to cycle between an inactive GDP-bound and an active GTP-bound form. Among the key regulators of GTPase cycling are the GTPase-activating proteins (GAPs), which stimulate the weak intrinsic GTP-hydrolysis activity of the GTPases, thereby inactivating them. Despite the abundance of GAPs and the fact that mutations in GAP-encoding genes underlie several human diseases, these proteins have received relatively little attention. Recent studies have addressed the regulatory mechanisms that influence GAP activity. So far, findings suggest that GAP activity is regulated by several mechanisms, including protein-protein interactions, phospholipid interactions, phosphorylation, subcellular translocation and proteolytic degradation.
引用
收藏
页码:377 / 385
页数:9
相关论文
共 62 条
[1]
AHMED S, 1995, METHOD ENZYMOL, V256, P114
[2]
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
[3]
Human mitotic spindle-associated protein PRC1 inhibits MgcRacGAP activity toward Cdc42 during the metaphase [J].
Ban, R ;
Irino, Y ;
Fukami, K ;
Tanaka, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (16) :16394-16402
[4]
GAPs galore! A survey of putative Ras superfamily GTPase activating proteins in man and Drosophila [J].
Bernards, A .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2003, 1603 (02) :47-82
[5]
Lipid packing sensed by ArfGAP1 couples COPI coat disassembly to membrane bilayer curvature [J].
Bigay, J ;
Gounon, P ;
Robineau, S ;
Antonny, B .
NATURE, 2003, 426 (6966) :563-566
[6]
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
[7]
DIFFERENTIAL REGULATION OF RASGAP AND NEUROFIBROMATOSIS GENE-PRODUCT ACTIVITIES [J].
BOLLAG, G ;
MCCORMICK, F .
NATURE, 1991, 351 (6327) :576-579
[8]
The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q [J].
Borkhardt, A ;
Bojesen, S ;
Haas, OA ;
Fuchs, U ;
Bartelheimer, D ;
Loncarevic, IF ;
Bohle, RM ;
Harbott, J ;
Repp, R ;
Jaeger, U ;
Viehmann, S ;
Henn, T ;
Korth, P ;
Scharr, D ;
Lampert, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :9168-9173
[9]
NF1 tumor suppressor gene function: Narrowing the GAP [J].
Cichowski, K ;
Jacks, T .
CELL, 2001, 104 (04) :593-604
[10]
Dynamic regulation of the Ras pathway via proteolysis of the NF1 tumor suppressor [J].
Cichowski, K ;
Santiago, S ;
Jardim, M ;
Johnson, BW ;
Jacks, T .
GENES & DEVELOPMENT, 2003, 17 (04) :449-454