Title | The SOCS box protein STOPS is required for phototransduction through its effects on phospholipase C |
Publication Type | Journal Article |
Year of Publication | 2008 |
Authors | Wang T, Wang X, Xie Q, Montell C |
Journal | Neuron |
Volume | 57 |
Pagination | 56-68 |
Date Published | 2008 Jan 10 |
ISSN | 0896-6273 |
Keywords | Animals, Animals, Genetically Modified, Antiporters, Drosophila melanogaster, Drosophila Proteins, Electroretinography, Gene Expression Regulation, GTP Phosphohydrolases, Hot Temperature, Membrane Potentials, Microtubule-Associated Proteins, Mutation, Phospholipase C beta, Photic Stimulation, Photoreceptor Cells, Photoreceptor Cells, Invertebrate, Protein Structure, Tertiary, Sequence Alignment, Suppressor of Cytokine Signaling Proteins, Type C Phospholipases, Vision, Ocular |
Abstract | Phosphoinositide-specific phospholipase C (PLC) isozymes play roles in a diversity of processes including Drosophila phototransduction. In fly photoreceptor cells, the PLCbeta encoded by norpA is critical for activation of TRP channels. Here, we describe a PLCbeta regulator, STOPS, which encodes a SOCS box protein. Mutation of stops resulted in a reduced concentration of NORPA and a defect in stopping signaling following cessation of the light stimulus. NORPA has been proposed to have dual roles as a PLC- and GTPase-activating protein (GAP). We found that the slow termination resulting from expressing low levels of wild-type NORPA was suppressed by addition of normal amounts of an altered NORPA, which had wild-type GAP activity, but no PLC activity. STOPS is the first protein identified that specifically regulates PLCbeta protein concentration. Moreover, this work demonstrates that a PLCbeta derivative that does not promote TRP channel activation, still contributes to signaling in vivo. |
DOI | 10.1016/j.neuron.2007.11.020 |
Alternate Journal | Neuron |
PubMed ID | 18184564 |
PubMed Central ID | PMC2253723 |
Grant List | EY08117 / EY / NEI NIH HHS / United States EY10852 / EY / NEI NIH HHS / United States R01 EY008117-19 / EY / NEI NIH HHS / United States R01 EY010852-14 / EY / NEI NIH HHS / United States |