G protein signaling from activated rat Frizzled-1 to the β-catenin-Lef-Tcf pathway

被引:202
作者
Liu, T
DeCostanzo, AJ
Liu, XX
Wang, HY
Hallagan, S
Moon, RT
Malbon, CC [1 ]
机构
[1] SUNY Stony Brook, Univ Med Ctr, Dept Mol Pharmacol, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Univ Med Ctr, Dept Physiol, Diabet & Metab Dis Res Ctr, Stony Brook, NY 11794 USA
[3] Univ Washington, Sch Med, Howard Hughes Med Inst, Dept Pharmacol, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Ctr Dev Biol, Seattle, WA 98195 USA
关键词
D O I
10.1126/science.1060100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The frizzled receptors, which mediate development and display seven hydrophobic, membrane-spanning segments, are cell membrane-localized. We constructed a chimeric receptor with the ligand-binding and transmembrane segments from the beta (2)-adrenergic receptor (beta (2)AR) and the cytoplasmic domains from rat Frizzled-1 (Rfz1). Stimulation of mouse F9 clones expressing the chimera (beta (2)AR-Rfz1) with the beta -adrenergic agonist isoproterenol stimulated stabilization of beta -catenin, activation. of a beta -catenin-sensitive promoter, and formation of primitive endoderm. The response was blocked by inactivation of pertussis toxin-sensitive, heterotrimeric guanine nucleotide-binding proteins (G proteins) and by depletion of G alphaq and G alphao. Thus, G proteins are elements of Wnt/Frizzled-1 signaling to the beta -catenin-lymphoid-enhancer factor (LEF)-T cell factor (Tcf) pathway.
引用
收藏
页码:1718 / 1722
页数:5
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