| First Author | Shinohara N | Year | 2011 |
| Journal | J Lipid Res | Volume | 52 |
| Issue | 11 | Pages | 1927-35 |
| PubMed ID | 21880860 | Mgi Jnum | J:263420 |
| Mgi Id | MGI:6189378 | Doi | 10.1194/jlr.M015081 |
| Citation | Shinohara N, et al. (2011) Enzymological analysis of the tumor suppressor A-C1 reveals a novel group of phospholipid-metabolizing enzymes. J Lipid Res 52(11):1927-35 |
| abstractText | A-C1 protein is the product of a tumor suppressor gene negatively regulating the oncogene Ras and belongs to the HRASLS (HRAS-like suppressor) subfamily. We recently found that four members of this subfamily expressed in human tissues function as phospholipid-metabolizing enzymes. Here we examined a possible enzyme activity of A-C1. The homogenates of COS-7 cells overexpressing recombinant A-C1s from human, mouse, and rat showed a phospholipase A(1/2) (PLA(1/2)) activity toward phosphatidylcholine (PC). This finding was confirmed with the purified A-C1. The activity was Ca(2)(+) independent, and dithiothreitol and Nonidet P-40 were indispensable for full activity. Phosphatidylethanolamine (PE) was also a substrate and the phospholipase A(1) (PLA(1)) activity was dominant over the PLA(2) activity. Furthermore, the protein exhibited acyltransferase activities transferring an acyl group of PCs to the amino group of PEs and the hydroxyl group of lyso PCs. As for tissue distribution in human, mouse, and rat, A-C1 mRNA was abundantly expressed in testis, skeletal muscle, brain, and heart. These results demonstrate that A-C1 is a novel phospholipid-metabolizing enzyme. Moreover, the fact that all five members of the HRASLS subfamily, including A-C1, show similar catalytic properties strongly suggests that these proteins constitute a new class of enzymes showing PLA(1/2) and acyltransferase activities. |
