Function and dysfunction of the PI system in membrane trafficking

被引:161
作者
Vicinanza, Mariella [1 ]
D'Angelo, Giovanni [1 ]
Di Campli, Antonella [1 ]
De Matteis, Maria Antonietta [1 ]
机构
[1] Consorzio Mario Negri Sud, Dept Cell Biol & Oncol, I-66030 Santa Maria Imbaro, CH, Italy
关键词
genetic diseases; membrane trafficking; phosphoinositides;
D O I
10.1038/emboj.2008.169
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 phosphoinositides (PIs) function as efficient and finely tuned switches that control the assembly-disassembly cycles of complex molecular machineries with key roles in membrane trafficking. This important role of the PIs is mainly due to their versatile nature, which is in turn determined by their fast metabolic interconversions. PIs can be tightly regulated both spatially and temporally through the many PI kinases (PIKs) and phosphatases that are distributed throughout the different intracellular compartments. In spite of the enormous progress made in the past 20 years towards the definition of the molecular details of PI-protein interactions and of the regulatory mechanisms of the individual PIKs and phosphatases, important issues concerning the general principles of the organisation of the PI system and the coordination of the different PI-metabolising enzymes remain to be addressed. The answers should come from applying a systems biology approach to the study of the PI system, through the integration of analyses of the protein interaction data of the PI enzymes and the PI targets with those of the 'phenomes' of the genetic diseases that involve these PI-metabolising enzymes.
引用
收藏
页码:2457 / 2470
页数:14
相关论文
共 142 条
  • [1] The activation of exocytotic sites by the formation of phosphatidylinositol 4,5-bisphosphate microdomains at syntaxin clusters
    Aoyagi, K
    Sugaya, T
    Umeda, M
    Yamamoto, S
    Terakawa, S
    Takahashi, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) : 17346 - 17352
  • [2] THE LOWE OCULOCEREBRORENAL SYNDROME GENE ENCODES A PROTEIN HIGHLY HOMOLOGOUS TO INOSITOL POLYPHOSPHATE-5-PHOSPHATASE
    ATTREE, O
    OLIVOS, IM
    OKABE, I
    BAILEY, LC
    NELSON, DL
    LEWIS, RA
    MCINNES, RR
    NUSSBAUM, RL
    [J]. NATURE, 1992, 358 (6383) : 239 - 242
  • [3] Bai JH, 2003, METHOD ENZYMOL, V360, P238
  • [4] Maintenance of hormone-sensitive phosphoinositide pools in the plasma membrane requires phosphatidylinositol 4-kinase IIIα
    Balla, Andras
    Kim, Yeun Ju
    Varnai, Peter
    Szentpetery, Zsofia
    Knight, Zachary
    Shokat, Kevan M.
    Balla, Tamas
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (02) : 711 - 721
  • [5] Organelle identity and the signposts for membrane traffic
    Behnia, R
    Munro, S
    [J]. NATURE, 2005, 438 (7068) : 597 - 604
  • [6] Membrane association of myotubularin-related protein 2 is mediated by a pleckstrin homology-GRAM domain and a coiled-coil dimerization module
    Berger, P
    Schaffitzel, C
    Berger, I
    Ban, N
    Suter, U
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) : 12177 - 12182
  • [7] Integration of Golgi trafficking and growth factor signaling by the lipid phosphatase SAC1
    Blagoveshchenskaya, Anastasia
    Cheong, Fei Ying
    Rohde, Holger M.
    Glover, Greta
    Knodler, Andreas
    Nicolson, Teresa
    Boehmelt, Guido
    Mayinger, Peter
    [J]. JOURNAL OF CELL BIOLOGY, 2008, 180 (04) : 803 - 812
  • [8] Osmotic stress-induced increase of phosphatidylinositol 3,5-bisphosphate requires Vac14p, an activator of the lipid kinase Fab1p
    Bonangelino, CJ
    Nau, JJ
    Duex, JE
    Brinkman, M
    Wurmser, AE
    Gary, JD
    Emr, SD
    Weisman, LS
    [J]. JOURNAL OF CELL BIOLOGY, 2002, 156 (06) : 1015 - 1028
  • [9] Phosphatidylinositol(3)-phosphate signaling mediated by specific binding to RING FYVE domains
    Burd, CG
    Emr, SD
    [J]. MOLECULAR CELL, 1998, 2 (01) : 157 - 162
  • [10] Dynamin is membrane-active: Lipid insertion is induced by phosphoinositides and phosphatidic acid
    Burger, KNJ
    Demel, RA
    Schmid, SL
    de Kruijff, B
    [J]. BIOCHEMISTRY, 2000, 39 (40) : 12485 - 12493