| Literature DB >> 22137581 |
Max R Banko1, Jasmina J Allen, Bethany E Schaffer, Erik W Wilker, Peiling Tsou, Jamie L White, Judit Villén, Beatrice Wang, Sara R Kim, Kei Sakamoto, Steven P Gygi, Lewis C Cantley, Michael B Yaffe, Kevan M Shokat, Anne Brunet.
Abstract
The energy-sensing AMP-activated protein kinase (AMPK) is activated by low nutrient levels. Functions of AMPK, other than its role in cellular metabolism, are just beginning to emerge. Here we use a chemical genetics screen to identify direct substrates of AMPK in human cells. We find that AMPK phosphorylates 28 previously unidentified substrates, several of which are involved in mitosis and cytokinesis. We identify the residues phosphorylated by AMPK in vivo in several substrates, including protein phosphatase 1 regulatory subunit 12C (PPP1R12C) and p21-activated protein kinase (PAK2). AMPK-induced phosphorylation is necessary for PPP1R12C interaction with 14-3-3 and phosphorylation of myosin regulatory light chain. Both AMPK activity and PPP1R12C phosphorylation are increased in mitotic cells and are important for mitosis completion. These findings suggest that AMPK coordinates nutrient status with mitosis completion, which may be critical for the organism's response to low nutrients during development, or in adult stem and cancer cells.Entities:
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Year: 2011 PMID： 22137581 PMCID： PMC3246132 DOI： 10.1016/j.molcel.2011.11.005
Source DB: PubMed Journal: Mol Cell ISSN： 1097-2765 Impact factor: 17.970