ADP-ribosylation factor (ARF)-like 4, 6, and 7 represent a subgroup of the ARF family characterized by rapid nucleotide exchange and a nuclear localization signal

被引:60
作者
Jacobs, S [1 ]
Schilf, C [1 ]
Fliegert, F [1 ]
Koling, S [1 ]
Weber, Y [1 ]
Schürmann, A [1 ]
Joost, HG [1 ]
机构
[1] Rhein Westfal TH Aachen, Fak Med, Inst Pharmacol & Toxicol, D-52057 Aachen, Germany
关键词
ADP-ribosylation factor; GTPase; Ras-related; GTP binding;
D O I
10.1016/S0014-5793(99)00759-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The novel ARF-like GTPase ARL7 is a close relative of ARL4 and ARL6 (71% and 59% identical amino acids). A striking characteristic of these GTPases is their basic C-terminus which, when fused to the C-terminus of green fluorescent protein (GFP), targets the constructs to the nucleus of transfected COS-7 cells. Full length ARL4 was detected in both nuclear and extranuclear compartments, whereas a construct of ARL4 lacking its C-terminus was excluded from the nucleus. Nucleotide exchange rates of recombinant ARL4, ARL6 and ARL7 were similar and appeared considerably higher than those of other members of the ARF family (ARF1, ARP), It is concluded that ARL4, ARL6 and ARL7 form a subgroup within the ARF family with similar, possibly nuclear, function. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:384 / 388
页数:5
相关论文
共 24 条
[1]   ARF PROTEINS - THE MEMBRANE TRAFFIC POLICE [J].
BOMAN, AL ;
KAHN, RA .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (04) :147-150
[2]   Cloning of a novel member (ARL5) of the ARF-family of ras-related GTPases [J].
Breiner, M ;
Schurmann, A ;
Becker, W ;
Joost, HG .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1996, 1308 (01) :1-6
[3]  
CAVENAGH MM, 1994, J BIOL CHEM, V269, P18937
[4]   SELECTIVE AMPLIFICATION OF ADDITIONAL MEMBERS OF THE ADP-RIBOSYLATION FACTOR (ARF) FAMILY - CLONING OF ADDITIONAL HUMAN AND DROSOPHILA ARF-LIKE GENES [J].
CLARK, J ;
MOORE, L ;
KRASINSKAS, A ;
WAY, J ;
BATTEY, J ;
TAMKUN, J ;
KAHN, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (19) :8952-8956
[5]   NUCLEAR TARGETING SEQUENCES - A CONSENSUS [J].
DINGWALL, C ;
LASKEY, RA .
TRENDS IN BIOCHEMICAL SCIENCES, 1991, 16 (12) :478-481
[6]   Phospholipase D: Enzymology, mechanisms of regulation, and function [J].
Exton, JH .
PHYSIOLOGICAL REVIEWS, 1997, 77 (02) :303-320
[7]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[8]   Protein kinesis - Nucleocytoplasmic transport [J].
Gorlich, D ;
Mattaj, IW .
SCIENCE, 1996, 271 (5255) :1513-1518
[9]   COMPARISON OF THE POSITIONAL CLONING METHODS USED TO ISOLATE THE BRCA1 GENE [J].
HARSHMAN, K ;
BELL, R ;
ROSENTHAL, J ;
KATCHER, H ;
MIKI, Y ;
SWENSON, J ;
GHOLAMI, Z ;
FRYE, C ;
DING, W ;
DAYANANTH, P ;
EDDINGTON, K ;
NORRIS, FH ;
BRISTOW, PK ;
PHELPS, R ;
HATTIER, T ;
STONE, S ;
SHAFFER, D ;
BAYER, S ;
HUSSEY, C ;
TRAN, T ;
RICHARDSON, K ;
DEHOFF, B ;
LAI, M ;
ROSTECK, PR ;
SKOLNICK, MH ;
SHATTUCKEIDENS, D ;
KAMB, A .
HUMAN MOLECULAR GENETICS, 1995, 4 (08) :1259-1266
[10]   Phospholipid- and GTP-dependent activation of cholera toxin and phospholipase D by human ADP-ribosylation factor-like protein 1 (HARL1) [J].
Hong, JX ;
Lee, FJS ;
Patton, WA ;
Lin, CY ;
Moss, J ;
Vaughan, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) :15872-15876