Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-10-24
pubmed:abstractText
The DLX homeodomain proteins control development of the basal ganglia and branchial arches. To identify co-factors that regulate DLX function we utilized the yeast two-hybrid assay, and found a DLX interacting protein (DIP2) which binds to the N-terminal region of DLX2 via a PDZ domain. DIP2 appears to be an alternatively spliced form of GRIP1, a protein known to bind AMPA glutamate receptors via PDZ domains. Thus, we named it GRIP1b. We provide evidence that GRIP1b can function as a transcriptional co-activator of DLX2 and DLX5. Glutamate receptors inhibit this co-activation. These results suggest that some PDZ proteins may regulate transcription via their interactions with homeodomain proteins. Furthermore, these results suggest a link between glutamate receptors, PDZ proteins and the DLX transcription factors, all of which are co-expressed in the developing basal ganglia.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Arabidopsis Proteins, http://linkedlifedata.com/resource/pubmed/chemical/DIP2 protein, Arabidopsis, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Distal-less homeobox proteins, http://linkedlifedata.com/resource/pubmed/chemical/Dlx5 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Dlx6 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/GAL4 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Ncoa2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Receptor Coactivator 2, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, AMPA, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Tes protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/glutamate receptor ionotropic..., http://linkedlifedata.com/resource/pubmed/chemical/glutamate receptor ionotropic...
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0165-3806
pubmed:author
pubmed:issnType
Print
pubmed:day
24
pubmed:volume
130
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
217-30
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:11675124-Alternative Splicing, pubmed-meshheading:11675124-Animals, pubmed-meshheading:11675124-Arabidopsis Proteins, pubmed-meshheading:11675124-Basal Ganglia, pubmed-meshheading:11675124-DNA-Binding Proteins, pubmed-meshheading:11675124-Enhancer Elements, Genetic, pubmed-meshheading:11675124-Fungal Proteins, pubmed-meshheading:11675124-Gene Expression Regulation, Developmental, pubmed-meshheading:11675124-Homeodomain Proteins, pubmed-meshheading:11675124-Mice, pubmed-meshheading:11675124-Nuclear Receptor Coactivator 2, pubmed-meshheading:11675124-Protein Structure, Tertiary, pubmed-meshheading:11675124-Receptors, AMPA, pubmed-meshheading:11675124-Saccharomyces cerevisiae Proteins, pubmed-meshheading:11675124-Transcription Factors, pubmed-meshheading:11675124-Transcriptional Activation, pubmed-meshheading:11675124-Two-Hybrid System Techniques, pubmed-meshheading:11675124-Yeasts
pubmed:year
2001
pubmed:articleTitle
Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, co-activates transcription with DLX homeodomain proteins.
pubmed:affiliation
Nina Ireland Laboratory of Developmental Neurobiology, Center for Neurobiology and Psychiatry, Department of Psychiatry, 401 Parnassus Avenue, University of California at San Francisco, CA 94143-0984, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't