RhoGDI: Multiple functions in the regulation of Rho family GTPase activities

被引:311
作者
Dovas, A [1 ]
Couchman, JR [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, London SW7 2AZ, England
基金
英国惠康基金;
关键词
effector; membrane domain; protein complex; Rho GDP-dissociation inhibitor (RhoGDI); Rho GTPase; targeting;
D O I
10.1042/BJ20050104
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
RhoGDI (Rho GDP-dissociation inhibitor) was identified as a down-regulator of Rho family GTPases typified by its ability to prevent nucleotide exchange and membrane association. Structural studies on GTPase-RhoGDI complexes, in combination with biochemical and cell biological results, have provided insight as to how RhoGDI exerts its effects on nucleotide binding, the membrane association-dissociation cycling of the GTPasc and how these activities are controlled. Despite the initial negative roles attributed to RhoGDI, recent evidence has come to suggest that it may also act as a positive regulator necessary for the correct targeting and regulation of Rho activities by conferring cues for spatial restriction, guidance and availability to effectors. These potential functions are discussed in the context of RhoGDI-associated multimolecular complexes, the newly emerged shuttling capability and the importance of the particular membrane microenvironment that represents the site of action for GTPases. All these results point to a wider role for RhoGDI than initially perceived, making it a binding partner that can tightly control Rho GTPases, but which also allows them to reach their full spectrum of activities.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 80 条
  • [1] ACTIVATION OF THE NADPH OXIDASE INVOLVES THE SMALL GTP-BINDING PROTEIN P21RAC1
    ABO, A
    PICK, E
    HALL, A
    TOTTY, N
    TEAHAN, CG
    SEGAL, AW
    [J]. NATURE, 1991, 353 (6345) : 668 - 670
  • [2] RhoGDI gamma: A GDP-dissociation inhibitor for Rho proteins with preferential expression in brain and pancreas
    Adra, CN
    Manor, D
    Ko, JL
    Zhu, SC
    Horiuchi, T
    VanAelst, L
    Cerione, RA
    Lim, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) : 4279 - 4284
  • [3] ERM-dependent movement of CD43 defines a novel protein complex distal to the immunological synapse
    Allenspach, EJ
    Cullinan, P
    Tong, JK
    Tang, QZ
    Tesciuba, AG
    Cannon, JL
    Takahashi, SM
    Morgan, R
    Burkhardt, JK
    Sperling, AI
    [J]. IMMUNITY, 2001, 15 (05) : 739 - 750
  • [4] Inhibition of RhoA by p120 catenin
    Anastasiadis, PZ
    Moon, SY
    Thoreson, MA
    Mariner, DJ
    Crawford, HC
    Zheng, Y
    Reynolds, AB
    [J]. NATURE CELL BIOLOGY, 2000, 2 (09) : 637 - 644
  • [5] Localization of AtROP4 and AtROP6 and interaction with the guanine nucleotide dissociation inhibitor AtRhoGDI1 from Arabidopsis
    Bischoff, F
    Vahlkamp, L
    Molendijk, A
    Palme, K
    [J]. PLANT MOLECULAR BIOLOGY, 2000, 42 (03) : 515 - 530
  • [6] Rho GTPases and their effector proteins
    Bishop, AL
    Hall, A
    [J]. BIOCHEMICAL JOURNAL, 2000, 348 (02) : 241 - 255
  • [7] Phosphorylation of Rho GDI stabilizes the Rho A-Rho GDI complex in neutrophil cytosol
    Bourmeyster, N
    Vignais, PV
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 218 (01) : 54 - 60
  • [8] ERM proteins and merlin: Integrators at the cell cortex
    Bretscher, A
    Edwards, K
    Fehon, RG
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (08) : 586 - 599
  • [9] RhoGDl-3 regulates RhoG and targets this protein to the Golgi complex through its unique N-terminal domain
    Brunet, N
    Morin, A
    Olofsson, B
    [J]. TRAFFIC, 2002, 3 (05) : 342 - 357
  • [10] Identification of two distinct mechanisms of phagocytosis controlled by different Rho GTPases
    Caron, E
    Hall, A
    [J]. SCIENCE, 1998, 282 (5394) : 1717 - 1721