Interactome Analysis Reveals Regulator of G Protein Signaling 14 (RGS14) is a Novel Calcium/Calmodulin (Ca2+/CaM) and CaM Kinase II (CaMKII) Binding Partner.
Paul R EvansKyle J GerberEric B DammerDuc M DuongDevrishi GoswamiDaniel J LustbergJuan ZouJenny J YangSerena M DudekPatrick R GriffinNicholas T SeyfriedJohn R HeplerPublished in: Journal of proteome research (2018)
Regulator of G Protein Signaling 14 (RGS14) is a complex scaffolding protein that integrates G protein and MAPK signaling pathways. In the adult mouse brain, RGS14 is predominantly expressed in hippocampal CA2 neurons where it naturally inhibits synaptic plasticity and hippocampus-dependent learning and memory. However, the signaling proteins that RGS14 natively engages to regulate plasticity are unknown. Here, we show that RGS14 exists in a high-molecular-weight protein complex in brain. To identify RGS14 neuronal interacting partners, endogenous RGS14 immunoprecipitated from mouse brain was subjected to mass spectrometry and proteomic analysis. We find that RGS14 interacts with key postsynaptic proteins that regulate plasticity. Gene ontology analysis reveals the most enriched RGS14 interactors have functional roles in actin-binding, calmodulin(CaM)-binding, and CaM-dependent protein kinase (CaMK) activity. We validate these findings using biochemical assays that identify interactions with two previously unknown binding partners. We report that RGS14 directly interacts with Ca2+/CaM and is phosphorylated by CaMKII in vitro. Lastly, we detect that RGS14 associates with CaMKII and CaM in hippocampal CA2 neurons. Taken together, these findings demonstrate that RGS14 is a novel CaM effector and CaMKII phosphorylation substrate thereby providing new insight into mechanisms by which RGS14 controls plasticity in CA2 neurons.
Keyphrases
- protein kinase
- mass spectrometry
- binding protein
- spinal cord
- transcription factor
- cerebral ischemia
- dna methylation
- hepatitis c virus
- dna binding
- amino acid
- genome wide
- blood brain barrier
- young adults
- human immunodeficiency virus
- tyrosine kinase
- immune response
- functional connectivity
- resting state
- copy number
- regulatory t cells
- endoplasmic reticulum stress
- single cell