RET receptor tyrosine kinase architecture, assemblies, and activation

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Authors: Mia Zol-Hanlon, Neil Q. McDonald
Cited by: 2
References: 60

Abstract

Among the 58 human receptor tyrosine kinases that are known, only the RET (REarrangement during Transfection) receptor contains cadherin-like domains in its extracellular portion. This multidomain extracellular module contains a binding site for a family of five related heterodimeric ligands. Each heterodimer comprises a secreted glial cell line-derived neurotrophic factor (GDNF) family ligand (GFL) and a membrane-anchored co-receptor GFR⍺ (GDNF family receptor alpha). Once a GFL-GFR⍺ ligand is bound to RET, this stimulates the activation of the receptor through tyrosine-based autophosphorylation. This mini review explores how the shape and architecture of RET encode a flexible GFL-GFR⍺-binding site, summarising recent progress in understanding RET structure. It then discusses current views on how distinct assemblies of GFL-GFR⍺-RET receptor complexes are able to activate the intrinsic RET tyrosine kinase function to relay intracellular signals.

Fields of Study & Subjects

Nerve injury and regeneration Wnt/β-catenin signaling in development and cancer Cancer-related Molecular Pathways

Publication details

Journal / source
Endocrine Related Cancer
Publisher
Bioscientifica
Volume
33
Issue
4
Publication date
1 April 2026
Language
EN