<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(19)</volume><submitter>Safdie G</submitter><pubmed_abstract>Brain function depends on a delicate balance between excitation and inhibition. Similarly, Caenorhabditis elegans motor system function depends on a precise balance between excitation and inhibition, as C. elegans muscles receive both inhibitory, GABAergic and excitatory, cholinergic inputs from motor neurons. Here we show that phosphorylation of the ER-resident chaperone of nicotinic acetylcholine receptors, RIC-3, leads to increased muscle excitability. RIC-3 phosphorylation at Ser-164 depends on opposing functions of the phosphatase calcineurin (TAX-6), and of the casein kinase II homologue KIN-10. Effects of calcineurin down-regulation and of phosphorylated RIC-3 on muscle excitability are mediated by GABAA receptor inhibition. Thus RIC-3 phosphorylation enables effects of this chaperone on GABAA receptors in addition to nAChRs. This dual effect provides coordinated regulation of excitation and inhibition and enables fine-tuning of the excitation-inhibition balance. Moreover, regulation of inhibitory GABAA signaling by calcineurin, a calcium- and calmodulin-dependent phosphatase, enables homeostatic balancing of excitation and inhibition.</pubmed_abstract><journal>Molecular biology of the cell</journal><pagination>2994-3003</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5042584</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>RIC-3 phosphorylation enables dual regulation of excitation and inhibition of Caenorhabditis elegans muscle.</pubmed_title><pmcid>PMC5042584</pmcid><pubmed_authors>Safdie G</pubmed_authors><pubmed_authors>Treinin M</pubmed_authors><pubmed_authors>Liewald JF</pubmed_authors><pubmed_authors>Kagan S</pubmed_authors><pubmed_authors>Gottschalk A</pubmed_authors><pubmed_authors>Battat E</pubmed_authors></additional><is_claimable>false</is_claimable><name>RIC-3 phosphorylation enables dual regulation of excitation and inhibition of Caenorhabditis elegans muscle.</name><description>Brain function depends on a delicate balance between excitation and inhibition. Similarly, Caenorhabditis elegans motor system function depends on a precise balance between excitation and inhibition, as C. elegans muscles receive both inhibitory, GABAergic and excitatory, cholinergic inputs from motor neurons. Here we show that phosphorylation of the ER-resident chaperone of nicotinic acetylcholine receptors, RIC-3, leads to increased muscle excitability. RIC-3 phosphorylation at Ser-164 depends on opposing functions of the phosphatase calcineurin (TAX-6), and of the casein kinase II homologue KIN-10. Effects of calcineurin down-regulation and of phosphorylated RIC-3 on muscle excitability are mediated by GABAA receptor inhibition. Thus RIC-3 phosphorylation enables effects of this chaperone on GABAA receptors in addition to nAChRs. This dual effect provides coordinated regulation of excitation and inhibition and enables fine-tuning of the excitation-inhibition balance. Moreover, regulation of inhibitory GABAA signaling by calcineurin, a calcium- and calmodulin-dependent phosphatase, enables homeostatic balancing of excitation and inhibition.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2021-02-25T08:08:00Z</modification><creation>2019-03-27T02:25:32Z</creation></dates><accession>S-EPMC5042584</accession><cross_references><pubmed>27489343</pubmed><doi>10.1091/mbc.E16-05-0265</doi></cross_references></HashMap>