Shisheva Assia
Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Cell Biol Int. 2008 Jun;32(6):591-604. doi: 10.1016/j.cellbi.2008.01.006. Epub 2008 Jan 25.
Key components of membrane trafficking and signaling machinery in eukaryotic cells are proteins that bind or synthesize phosphoinositides. PIKfyve, a product of an evolutionarily conserved single-copy gene has both these features. It binds to membrane phosphatidylinositol (PtdIns)3P and synthesizes PtdIns(3,5)P2 and PtdIns5P. Molecular functions of PIKfyve are elusive but recent advances are consistent with a key role in the course of endosomal transport. PIKfyve dysfunction induces endosome enlargement and profound cytoplasmic vacuolation, likely as a result of impaired normal endosome processing and membrane exit out of endosomes. Multicellular organisms with genetically impaired function of PIKfyve or that of the PIKfyve protein partners regulating PtdIns(3,5)P2 homeostasis display severe disorders, including embryonic/perinatal death. This review describes recent advances on PIKfyve functionality in higher eukaryotes, with particular reference to biochemical and genetic insights in PIKfyve protein partners.
真核细胞中膜运输和信号传导机制的关键组成部分是结合或合成磷酸肌醇的蛋白质。PIKfyve是一个进化上保守的单拷贝基因的产物,具备这两种功能。它与膜磷脂酰肌醇(PtdIns)3P结合,并合成PtdIns(3,5)P2和PtdIns5P。PIKfyve的分子功能尚不明确,但最近的研究进展表明它在内体运输过程中起关键作用。PIKfyve功能障碍会导致内体扩大和严重的细胞质空泡化,这可能是由于正常内体加工受损以及内体膜排出受阻所致。PIKfyve功能基因受损或调节PtdIns(3,5)P2稳态的PIKfyve蛋白伴侣功能基因受损的多细胞生物会出现严重紊乱,包括胚胎/围产期死亡。本综述描述了高等真核生物中PIKfyve功能的最新进展,特别提及了PIKfyve蛋白伴侣的生化和遗传学研究成果。