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Mol Cell. 2010 May 28;38(4):500-11. doi: 10.1016/j.molcel.2010.05.009.

Negative regulation of Vps34 by Cdk mediated phosphorylation.

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1
Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

Abstract

Vacuolar protein sorting 34 (Vps34) complexes, the class III PtdIns3 kinase, specifically phosphorylate the D3 position of PtdIns to produce PtdIns3P. Vps34 is involved in the control of multiple key intracellular membrane trafficking pathways including endocytic sorting and autophagy. In mammalian cells, Vps34 interacts with Beclin 1, an ortholog of Atg6 in yeast, to regulate the production of PtdIns3P and autophagy. We show that Vps34 is phosphorylated on Thr159 by Cdk1, which negatively regulates its interaction with Beclin 1 during mitosis. Cdk5/p25, a neuronal Cdk shown to play a role in Alzheimer's disease, can also phosphorylate Thr159 of Vps34. Phosphorylation of Vps34 on Thr159 inhibits its interaction with Beclin 1. We propose that phosphorylation of Thr159 in Vps34 is a key regulatory mechanism that controls the class III PtdIns3 kinase activity in cell-cycle progression, development, and human diseases including neurodegeneration and cancers.

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PMID:
20513426
PMCID:
PMC2888511
DOI:
10.1016/j.molcel.2010.05.009
[Indexed for MEDLINE]
Free PMC Article
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