| Literature DB >> 17827707 |
Yasunori Kanaho1, Akiko Kobayashi-Nakano, Takeaki Yokozeki.
Abstract
The phosphoinositide kinase, phosphatidylinositol 4-phosphate 5-kinase (PIP5K), produces the versatile phospholipid phosphatidylinositol 4,5-bisphosphate (PI4,5P(2)), through which PIP5K plays crucial roles in a wide variety of cell functions. So far, three PIP5K isozymes and splicing variants have been identified. We speculate that each PIP5K isozyme or splicing variant is activated in a tempo-spatially different manner, due to the existence of activators or recruiters specific to each isozyme: this tempo-spatially different activation of PIP5K produces PI4,5P(2) at different compartments of the cell at different times, which phenomenon may be responsible for the apparent multifunction of PI4,5P(2)/PIP5K. Accumulating evidence supports this notion that each PIP5K isozyme is activated by its specific activator and plays a crucial role in a unique cell function. In this article, we describe recent advances regarding the PIP5K isozyme-specific activation mechanisms and physiological functions.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17827707 DOI: 10.1248/bpb.30.1605
Source DB: PubMed Journal: Biol Pharm Bull ISSN: 0918-6158 Impact factor: 2.233