RET receptor tyrosine kinase architecture, assemblies, and activation

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.

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Publication Details

Journal
Endocrine Related Cancer
Published
2026-04-01
DOI
https://doi.org/10.1530/erc-25-0322
Primary Topic
Nerve injury and regeneration
Type
article
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article

RET receptor tyrosine kinase architecture, assemblies, and activation

Mia Zol-Hanlon, Neil Q. McDonald
Endocrine Related Cancer
Nerve injury and regeneration
article

RET receptor tyrosine kinase architecture, assemblies, and activation

Mia Zol-Hanlon, Neil Q. McDonald
article en

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.

Endocrine Related CancerVol. 33(4)
The Francis Crick Institute (GB), Birkbeck, University of London (GB)
Openalex Percentile: Top 28%
Nerve injury and regeneration
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RET receptor tyrosine kinase architecture, assemblies, and activation — Mia Zol-Hanlon, Neil Q. McDonald · Endocrine Related Cancer (2026) | TGRS Research Map | TGRS