Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2004-1-14
pubmed:abstractText
Wnt-Frizzled signaling via heterotrimeric G-proteins controls various aspects of early development. Because Wnts may activate more than one Frizzled, understanding the downstream signaling mechanisms and target genes for Frizzled activation has been a challenge. We constructed functional, chimeric receptors with the ligand-binding and transmembrane segments from the beta2-adrenergic receptor and the cytoplasmic domains from either rat Frizzled-1 (Rfz1) or Frizzled-2 (Rfz2). Activation with beta-agonist enables stimulation of only a single Frizzled pathway and profiling of genes targeted by this Frizzled-specific approach. Genes activated in mouse totipotent F9 teratocarcinoma cells solely by activation of the Rfz1 chimera include Lefty1, STAM, JAB, Erk1, MyD118, Fcer Ig, and follistatin, genes implicated in development. Stimulation of Rfz2 chimera, but not Rfz1, leads to activation of a smaller set of genes, including those for REST/NRSF, Groucho, nucleophosmin, and Ubc4/5E2. Activation of either Rfz1- or Rfz2-specific chimera leads, in these totipotent stem cells, to some differential activation of a common set of genes, including those for Msx-1, Msx-2, CBP/P300-associated factor, ephrin A3, and Nip-3. We demonstrate the utility of beta2-adrenergic receptor-Frizzled chimeras to provide the tools with which to activate and to probe Frizzled-specific downstream signaling to gene activation.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0026-895X
pubmed:author
pubmed:issnType
Print
pubmed:volume
65
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
45-55
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed:year
2004
pubmed:articleTitle
Gene profiling of Frizzled-1 and Frizzled-2 signaling: expression of G-protein-coupled receptor chimeras in mouse F9 teratocarcinoma embryonal cells.
pubmed:affiliation
Department of Pharmacology, Health Science Center, SUNY-Stony Brook, Stony Brook, NY 11794-8651, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't