The receptor tyrosine kinase Ror2 is involved in non‐canonical Wnt5a/JNK signalling pathway

Isao Oishi(Kobe University), Hiroaki Suzuki(Kobe University), Nobuyuki Onishi(Kobe University), Ritsuko Takada(Japan Science and Technology Agency), Shuichi Kani(Kobe University), Bisei Ohkawara(Tokyo Medical and Dental University), Ikue Koshida(Japan Science and Technology Agency), Kentaro Suzuki(Kumamoto University), General Yamada(Kumamoto University), Georg C. Schwabe(Max Planck Institute for Molecular Genetics), Stefan Mundlos(Max Planck Institute for Molecular Genetics), Hiroshi Shibuyà(Tokyo Medical and Dental University), Shinji Takada(Kyoto University), Yasuhiro Minami(Kobe University)
Genes to Cells
July 1, 2003
Cited by 792Open Access
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Abstract

BACKGROUND: Ror2 is an orphan receptor, belonging to the Ror family of receptor tyrosine kinases. Although Ror2 has been shown to play crucial roles in developmental morphogenesis, the precise signalling events that Ror2 mediates remain elusive. Since Ror2 possesses an extracellular cysteine-rich domain (CRD) that resembles the Wnt-binding sites of the Frizzled (Fz) proteins, it is conceivable that Ror2 interacts with members of the Wnt family. RESULTS: Both Ror2-/- and Wnt5a-/- mice exhibit dwarfism, facial abnormalities, short limbs and tails, dysplasia of lungs and genitals, and ventricular septal defects. In vitro binding assay revealed that Wnt5a binds to the CRD of Ror2. Furthermore, Ror2 associates via its CRD with rFz2, a putative receptor for Wnt5a. Interestingly, Wnt5a and Ror2 activate the non-canonical Wnt pathway, as assessed by activation of JNK in cultured cells and inhibition of convergent extension movements in Xenopus. CONCLUSIONS: Our findings indicate that Wnt5a and Ror2 interact physically and functionally. Ror2 may thus act as a receptor for Wnt5a to activate non-canonical Wnt signalling.


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