| First Author | Ren H | Year | 2010 |
| Journal | Mol Biol Cell | Volume | 21 |
| Issue | 18 | Pages | 3171-81 |
| PubMed ID | 20660155 | Mgi Jnum | J:182849 |
| Mgi Id | MGI:5316960 | Doi | 10.1091/mbc.E10-01-0073 |
| Citation | Ren H, et al. (2010) A phosphatidic acid binding/nuclear localization motif determines lipin1 function in lipid metabolism and adipogenesis. Mol Biol Cell 21(18):3171-81 |
| abstractText | Lipins are phosphatidic acid phosphatases with a pivotal role in regulation of triglyceride and glycerophospholipid metabolism. Lipin1 is also an amplifier of PGC-1alpha, a nuclear coactivator of PPAR-alpha responsive gene transcription. Lipins do not contain recognized membrane-association domains, but interaction of these enzymes with cellular membranes is necessary for access to their phospholipid substrate. We identified a role for a conserved polybasic amino acid motif in an N-terminal domain previously implicated as a determinant of nuclear localization in selective binding of lipin1beta to phosphatidic acid, using blot overlay assays and model bilayer membranes. Studies using lipin1beta polybasic motif variants establish that this region is also critical for nuclear import and raise the possibility that nuclear/cytoplasmic shuttling of lipin1beta is regulated by PA. We used pharmacological agents and lipin1beta polybasic motif mutants to explore the role of PA-mediated membrane association and nuclear localization on lipin1beta function in phospholipid metabolism and adipogenic differentiation. We identify a role for the lipin1 polybasic motif as both a lipid binding motif and a primary nuclear localization sequence. These two functions are necessary for full expression of the biological activity of the protein in intracellular lipid metabolism and transcriptional control of adipogenesis. |
