PIP5K1A (phosphatidylinositol-4-phosphate 5-kinase type 1 alpha)

	Figure 1. Schematic representation of human PIP5K1A isoform with the conserved kinase core domain (adopted from Porciello 2016).
Description	PIP5K1A is a 61-kDa protein migrating at about 68 kDa in SDS-PAGE (Fruman 1998). The protein shows 83% and 35% amino acid identity with PIP5K1B and PIP4K2A (PIP5K2A), respectively, within the conserved kinase homology domain (Loijens 1996). Overall, the PIP5K1A and PIP5K1B proteins are 64% identical and Northern analysis shows the two to have a wide tissue distributions, but greatly differing expression levels. Recombinant, bacterially expressed PIP5KA was observed to have PIP5K activity and to be immunoreactive with erythroid PIP5KI antibodies (Loijens 1996). Furthermore, the authors isolated additional PIP5K1A cDNAs which they suggested represent splicing isoforms. Overexpression of mouse PIP5K1A in COS-7 cells stimulates an increase in short actin fibers and a decrease in actin stress fibers (Ishihara 1998). PIP5K1A mediate the phosphorylation of phosphatidylinositol 4-phosphate on the D5 position of the inositol ring, thus inducing the production of phosphatidylinositol 4,5-biphosphate (PIP2) (van den Bout 2009). In both humans and mice, all PIP5K isoforms show variation in their sequence by alternative splicing (Ishihara 1998). Three PIP5K1α, four β, and one γ splice variants were identified in humans and eight PIP5K1α, two β, and three γ splice variants are present in mice. (Ishihara 1998). All PIP5K isoforms α, β, and γ, and splice variants have a highly conserved kinase core domain that consists of 330-380 amino acids (Fig. 1), and a sub-domain called the activation loop, that regulates their activity and subcellular localization (Tuosto 2015). The variables N- and C-termini of PIP5K isoforms are also involved in the regulation of lipid kinase activity and in targeting PIP5Ks to specific cellular compartments (Kwiatkowska 2010). The C-terminal residues (440-562) of PIP5K1A regulate its localization at nuclear speckles (Mellman 2008). The 83 C-terminal amino acids of PIP5K1β are essential for its polarization at the uropod (Lacalle 2007), whereas the N-terminus controls PIP5K1β targeting to the plasma membrane and its dimerization with other PIP5K isoforms (Lacalle 2015). (Ishihara 1998). The crystal structure of the catalytic domain of zebrafish PIP5K1A has been reported at 3.3Å resolution and the molecule forms a side-to-side dimer (Hu 2015). Mutagenesis study of PIP5K1A indicated two adjacent interfaces for the dimerization and interaction with the DIX domain of the Wnt signalling molecule dishevelled. Much as the interfaces were located distally to the catalytic/substrate-binding site, binding to these interfaces either through dimerization or the interaction with DIX stimulated PIP5K1 catalytic activity. DIX binding additionally enhanced PIP5K1 substrate binding (Hu 2015). (Ishihara 1998). All the three PIP5K isoforms are expressed by primary T cells (Sun 2011) and they are triggered by phosphatidic acid (PA), which is generated by phospholipase D (PLD), through the hydrolysis of phosphatidylcholine (Jenkins 1994, Moritz 1992). PIP5K1α cooperates with PIP5Kβ and VAV1 in promoting actin polymerization and CD28 signaling functions in human T lymphocytes (Porciello 2016). PIP5K1A localises to the plasma membrane and the Golgi complex, and has also been observed at sites of membrane ruffling induced by the Rho GTPase RAC1 (van den Bout 2009). PIP5K1A in particular is recruited to the plasma membrane in response to several receptors to provide the substrate PIP2 for PLCγ leading to IP3 formation and Ca2+ mobilization (Saito 2003, Wang 2008 and Xie 2009). Both PIP5K1α and PIP5Kγ are known to interact and colocalize with phospholipase D 2 ( PLD2) at the membrane to stimulate cell adhesion (Divecha 2000, Powner 2005). Some studies have also shown pronounced association of PIP5K1A with nuclear speckles (Chakrabarti 2013) where it may regulate pre-mRNA processing and mRNA export (Barlow 2010).
Function	Treatment of primary cultured astrocytes with gangliosides significantly enhanced PIP5K1α mRNA and protein expression levels (Sang 2010). MicroRNA-based PIP5K1α knockdown strongly reduced ganglioside-induced transcription of proinflammatory cytokines. In addition, PIP5K1α knockdown suppressed phosphorylation and nuclear translocation of NF-kB (Sang 2010). PIPK-mediated mechanisms regulate microtubule dynamics in neuronal development (Noda 2012). Using immunoprecipitation with an antibody specific to KIF2A, PIPKα was identified as a candidate membrane protein that regulates the activity of KIF2A. Yeast two-hybrid and biochemical assays showed direct binding between KIF2A and PIPKα. Furthermore, the microtubule (MT)- depolymerizing activity of KIF2A was enhanced in the presence of PIPKα in vitro and in vivo.

Search in all EBI   NCBI

For comments and suggestions or contributions, please contact us