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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2001-4-26
pubmed:abstractText
We have used a yeast two-hybrid approach to uncover protein interactions involving the D2-like subfamily of dopamine receptors. Using the third intracellular loop of the D2S and D3 dopamine receptors as bait to screen a human brain cDNA library, we identified filamin A (FLN-A) as a protein that interacts with both the D2 and D3 subtypes. The interaction with FLN-A was specific for the D2 and D3 receptors and was independently confirmed in pull-down and coimmunoprecipitation experiments. Deletion mapping localized the dopamine receptor-FLN-A interaction to the N-terminal segment of the D2 and D3 dopamine receptors and to repeat 19 of FLN-A. In cultures of dissociated rat striatum, FLN-A and D2 receptors colocalized throughout neuronal somata and processes as well as in astrocytes. Expression of D2 dopamine receptors in FLN-A-deficient M2 melanoma cells resulted in predominant intracellular localization of the D2 receptors, whereas in FLN-A-reconstituted cells, the D2 receptor was predominantly localized at the plasma membrane. These results suggest that FLN-A may be required for proper cell surface expression of the D2 dopamine receptors. Association of D2 and D3 dopamine receptors with FLN-A provides a mechanism whereby specific dopamine receptor subtypes may be functionally linked to downstream signaling components via the actin cytoskeleton.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10051605, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10373412, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10377350, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10617615, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10659839, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10692483, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10753124, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10890919, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-10999936, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-11163774, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-1332033, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-1833070, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-2042108, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-2391361, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-2594196, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-2856162, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-4063818, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-6879197, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-7534799, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-7569905, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-7904756, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-8384581, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-8494342, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9006895, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9006936, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9009191, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9367441, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9437013, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9636219, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9759378, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9804783, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9853904, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9883725, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9891976, http://linkedlifedata.com/resource/pubmed/commentcorrection/11320256-9892354
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
24
pubmed:volume
98
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5258-63
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:11320256-Actins, pubmed-meshheading:11320256-Animals, pubmed-meshheading:11320256-Binding Sites, pubmed-meshheading:11320256-Cells, Cultured, pubmed-meshheading:11320256-Contractile Proteins, pubmed-meshheading:11320256-Cytoskeleton, pubmed-meshheading:11320256-Fluorescent Antibody Technique, pubmed-meshheading:11320256-Humans, pubmed-meshheading:11320256-Melanoma, pubmed-meshheading:11320256-Microfilament Proteins, pubmed-meshheading:11320256-Models, Biological, pubmed-meshheading:11320256-Neostriatum, pubmed-meshheading:11320256-Precipitin Tests, pubmed-meshheading:11320256-Protein Binding, pubmed-meshheading:11320256-Protein Structure, Tertiary, pubmed-meshheading:11320256-Rats, pubmed-meshheading:11320256-Receptors, Dopamine D2, pubmed-meshheading:11320256-Receptors, Dopamine D3, pubmed-meshheading:11320256-Sequence Deletion, pubmed-meshheading:11320256-Substrate Specificity, pubmed-meshheading:11320256-Tumor Cells, Cultured, pubmed-meshheading:11320256-Two-Hybrid System Techniques
pubmed:year
2001
pubmed:articleTitle
Dopamine D2 and D3 receptors are linked to the actin cytoskeleton via interaction with filamin A.
pubmed:affiliation
Neuroscience Graduate Program, Department of Pharmacology, Penn State College of Medicine, Hershey, PA 17033, USA.
pubmed:publicationType
Journal Article
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