Source:http://linkedlifedata.com/resource/pubmed/id/16880127
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2006-8-1
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pubmed:abstractText |
The ability of CaMKII to act as a molecular switch, becoming Ca(2+) independent after activation and autophosphorylation at T287, is critical for experience-dependent plasticity. Here, we show that the Drosophila homolog of CASK, also known as Camguk, can act as a gain controller on the transition to calcium-independence in vivo. Genetic loss of dCASK significantly increases synapse-specific, activity-dependent autophosphorylation of CaMKII T287. In wild-type adult animals, simple and complex sensory stimuli cause region-specific increases in pT287. dCASK-deficient adults have a reduced dynamic range for activity-dependent T287 phosphorylation and have circuit-level defects that result in inappropriate activation of the kinase. dCASK control of the CaMKII switch occurs via its ability to induce autophosphorylation of T306 in the kinase's CaM binding domain. Phosphorylation of T306 blocks Ca(2+)/CaM binding, lowering the probability of intersubunit T287 phosphorylation, which requires CaM binding to both the substrate and catalytic subunits. dCASK is the first CaMKII-interacting protein other than CaM found to regulate this plasticity-controlling molecular switch.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CASK kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Caki protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent...,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent...,
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Guanylate Kinase
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0896-6273
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
327-37
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pubmed:dateRevised |
2010-12-3
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pubmed:meshHeading |
pubmed-meshheading:16880127-Animals,
pubmed-meshheading:16880127-Calcium-Calmodulin-Dependent Protein Kinase Type 2,
pubmed-meshheading:16880127-Calcium-Calmodulin-Dependent Protein Kinases,
pubmed-meshheading:16880127-Drosophila,
pubmed-meshheading:16880127-Drosophila Proteins,
pubmed-meshheading:16880127-Electric Stimulation,
pubmed-meshheading:16880127-Enzyme Activation,
pubmed-meshheading:16880127-Female,
pubmed-meshheading:16880127-Guanylate Kinase,
pubmed-meshheading:16880127-Ion Channel Gating,
pubmed-meshheading:16880127-Male,
pubmed-meshheading:16880127-Phosphorylation,
pubmed-meshheading:16880127-Retina,
pubmed-meshheading:16880127-Synapses
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pubmed:year |
2006
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pubmed:articleTitle |
Activity-dependent gating of CaMKII autonomous activity by Drosophila CASK.
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pubmed:affiliation |
Department of Biology, National Center for Behavioral Genomics and Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, N.I.H., Extramural
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