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Classes of Phosphoinositide 3-kinases at a Glance

Overview
Journal J Cell Sci
Specialty Cell Biology
Date 2014 Mar 4
PMID 24587488
Citations 165
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Abstract

The phosphoinositide 3-kinase (PI3K) family is important to nearly all aspects of cell and tissue biology and central to human cancer, diabetes and aging. PI3Ks are spatially regulated and multifunctional, and together, act at nearly all membranes in the cell to regulate a wide range of signaling, membrane trafficking and metabolic processes. There is a broadening recognition of the importance of distinct roles for each of the three different PI3K classes (I, II and III), as well as for the different isoforms within each class. Ongoing issues include the need for a better understanding of the in vivo complexity of PI3K regulation and cellular functions. This Cell Science at a Glance article and the accompanying poster summarize the biochemical activities, cellular roles and functional requirements for the three classes of PI3Ks. In doing so, we aim to provide an overview of the parallels, the key differences and crucial interplays between the regulation and roles of the three PI3K classes.

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References
1.
Munday A, Norris F, Caldwell K, Brown S, MAJERUS P, Mitchell C . The inositol polyphosphate 4-phosphatase forms a complex with phosphatidylinositol 3-kinase in human platelet cytosol. Proc Natl Acad Sci U S A. 1999; 96(7):3640-5. PMC: 22347. DOI: 10.1073/pnas.96.7.3640. View

2.
Shin H, Hayashi M, Christoforidis S, Lacas-Gervais S, Hoepfner S, Wenk M . An enzymatic cascade of Rab5 effectors regulates phosphoinositide turnover in the endocytic pathway. J Cell Biol. 2005; 170(4):607-18. PMC: 2171494. DOI: 10.1083/jcb.200505128. View

3.
Patrucco E, Notte A, Barberis L, Selvetella G, Maffei A, Brancaccio M . PI3Kgamma modulates the cardiac response to chronic pressure overload by distinct kinase-dependent and -independent effects. Cell. 2004; 118(3):375-87. DOI: 10.1016/j.cell.2004.07.017. View

4.
Falasca M, Maffucci T . Regulation and cellular functions of class II phosphoinositide 3-kinases. Biochem J. 2012; 443(3):587-601. DOI: 10.1042/BJ20120008. View

5.
Kurek K, Luks V, Ayturk U, Alomari A, Fishman S, Spencer S . Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome. Am J Hum Genet. 2012; 90(6):1108-15. PMC: 3370283. DOI: 10.1016/j.ajhg.2012.05.006. View