PubMed 26195823
Referenced in: none
Automatically associated channels: TRP , TRPM , TRPML , TRPML1
Title: The mucolipidosis IV Ca2+ channel TRPML1 (MCOLN1) is regulated by the TOR kinase.
Authors: Rob U Onyenwoke, Jonathan Z Sexton, Feng Yan, María Cristina Huertas Díaz, Lawrence J Forsberg, Michael B Major, Jay E Brenman
Journal, date & volume: Biochem. J., 2015 Sep 15 , 470, 331-42
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26195823
Abstract
Autophagy is a complex pathway regulated by numerous signalling events that recycles macromolecules and may be perturbed in lysosomal storage disorders (LSDs). During autophagy, aberrant regulation of the lysosomal Ca(2+) efflux channel TRPML1 [transient receptor potential mucolipin 1 (MCOLN1)], also known as MCOLN1, is solely responsible for the human LSD mucolipidosis type IV (MLIV); however, the exact mechanisms involved in the development of the pathology of this LSD are unknown. In the present study, we provide evidence that the target of rapamycin (TOR), a nutrient-sensitive protein kinase that negatively regulates autophagy, directly targets and inactivates the TRPML1 channel and thereby functional autophagy, through phosphorylation. Further, mutating these phosphorylation sites to unphosphorylatable residues proved to block TOR regulation of the TRPML1 channel. These findings suggest a mechanism for how TOR activity may regulate the TRPML1 channel.