The role of the phosphoinositides at the Golgi complex
- PMID: 15979509
- DOI: 10.1016/j.bbamcr.2005.04.013
The role of the phosphoinositides at the Golgi complex
Abstract
The phosphorylated derivatives of phosphatidylinositol (PtdIns), known as the polyphosphoinositides (PIs), represent key membrane-localized signals in the regulation of fundamental cell processes, such as membrane traffic and cytoskeleton remodelling. The reversible production of the PIs is catalyzed through the combined activities of a number of specific phosphoinositide phosphatases and kinases that can either act separately or in concert on all the possible combinations of the 3, 4, and 5 positions of the inositol ring. So far, seven distinct PI species have been identified in mammalian cells and named according to their site(s) of phosphorylation: PtdIns 3-phosphate (PI3P); PtdIns 4-phosphate (PI4P); PtdIns 5-phosphate (PI5P); PtdIns 3,4-bisphosphate (PI3,4P2); PtdIns 4,5-bisphosphate (PI4,5P2); PtdIns 3,5-bisphosphate (PI3,5P2); and PtdIns 3,4,5-trisphosphate (PI3,4,5P3). Over the last decade, accumulating evidence has indicated that the different PIs serve not only as intermediates in the synthesis of the higher phosphorylated phosphoinositides, but also as regulators of different protein targets in their own right. These regulatory actions are mediated through the direct binding of their protein targets. In this way, the PIs can control the subcellular localization and activation of their various effectors, and thus execute a variety of cellular responses. To exert these functions, the metabolism of the PIs has to be finely regulated both in time and space, and this is achieved by controlling the subcellular distribution, regulation, and activation states of the enzymes involved in their synthesis and removal (kinases and phosphatases). These exist in many different isoforms, each of which appears to have a distinctive intracellular localization and regulation. As a consequence of this subcompartimentalized PI metabolism, a sort of "PI-fingerprint" of each cell membrane compartment is generated. When combined with the targeted recruitment of their protein effectors and the different intracellular distributions of other lipids and regulatory proteins (such as small GTPases), these factors can maintain and determine the identity of the cell organelles despite the extensive membrane flux []. Here, we provide an overview of the regulation and roles of different phosphoinositide kinases and phosphatases and their lipid products at the Golgi complex.
Similar articles
-
Phosphatidylinositol Kinases and Phosphatases in Entamoeba histolytica.Front Cell Infect Microbiol. 2019 Jun 6;9:150. doi: 10.3389/fcimb.2019.00150. eCollection 2019. Front Cell Infect Microbiol. 2019. PMID: 31245297 Free PMC article. Review.
-
The multiple roles of PtdIns(4)P -- not just the precursor of PtdIns(4,5)P2.J Cell Sci. 2008 Jun 15;121(Pt 12):1955-63. doi: 10.1242/jcs.023630. J Cell Sci. 2008. PMID: 18525025 Review.
-
[Phosphoinositides: lipidic essential actors in the intracellular traffic].Biol Aujourdhui. 2015;209(1):97-109. doi: 10.1051/jbio/2015006. Epub 2015 Jun 26. Biol Aujourdhui. 2015. PMID: 26115715 French.
-
The role of the phosphoinositides at the Golgi complex.Biochem Soc Symp. 2007;(74):107-16. doi: 10.1042/BSS0740107. Biochem Soc Symp. 2007. PMID: 17233584 Review.
-
Sac1 lipid phosphatase and Stt4 phosphatidylinositol 4-kinase regulate a pool of phosphatidylinositol 4-phosphate that functions in the control of the actin cytoskeleton and vacuole morphology.Mol Biol Cell. 2001 Aug;12(8):2396-411. doi: 10.1091/mbc.12.8.2396. Mol Biol Cell. 2001. PMID: 11514624 Free PMC article.
Cited by
-
The Genetic Background of Abnormalities in Metabolic Pathways of Phosphoinositides and Their Linkage with the Myotubular Myopathies, Neurodegenerative Disorders, and Carcinogenesis.Biomolecules. 2023 Oct 19;13(10):1550. doi: 10.3390/biom13101550. Biomolecules. 2023. PMID: 37892232 Free PMC article. Review.
-
Mechanisms of Nonvesicular Ceramide Transport.Contact (Thousand Oaks). 2023 Oct 17;6:25152564231208250. doi: 10.1177/25152564231208250. eCollection 2023 Jan-Dec. Contact (Thousand Oaks). 2023. PMID: 37859671 Free PMC article. Review.
-
Phafins Are More Than Phosphoinositide-Binding Proteins.Int J Mol Sci. 2023 Apr 30;24(9):8096. doi: 10.3390/ijms24098096. Int J Mol Sci. 2023. PMID: 37175801 Free PMC article. Review.
-
Impact of interorganelle coordination between the conventional early secretory pathway and autophagy in cellular homeostasis and stress response.Front Cell Dev Biol. 2023 Apr 21;11:1069256. doi: 10.3389/fcell.2023.1069256. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37152281 Free PMC article. Review.
-
Fast-Killing Tyrosine Amide ((S)-SW228703) with Blood- and Liver-Stage Antimalarial Activity Associated with the Cyclic Amine Resistance Locus (PfCARL).ACS Infect Dis. 2023 Mar 10;9(3):527-539. doi: 10.1021/acsinfecdis.2c00527. Epub 2023 Feb 10. ACS Infect Dis. 2023. PMID: 36763526 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous
