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PMID: 8047140 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Mechanism of activation of the TGF-beta receptor.

Nature ·Vol. 370 ·No. 6488 ·1994-08-04 ·Pages 341-7

Wrana JL, Attisano L, Wieser R, Ventura F, Massagué J

Abstract

Transforming growth factor-beta (TGF-beta) signals by contacting two distantly related transmembrane serine/threonine kinases called receptors I and II. The role of these molecules in signalling has now been determined. TGF-beta binds directly to receptor II, which is a constitutively active kinase. Bound TGF-beta is then recognized by receptor I which is recruited into the complex and becomes phosphorylated by receptor II. Phosphorylation allows receptor I to propagate the signal to downstream substrates. This provides a mechanism by which a cytokine can generate the first step of a signalling cascade.

MeSH Terms
Amino Acid Sequence Animals Cell Line Cell Membrane/metabolism Humans Mink Molecular Sequence Data Phosphorus Radioisotopes Phosphorylation Protein Serine-Threonine Kinases Receptor Protein-Tyrosine Kinases/metabolism Receptor, Transforming Growth Factor-beta Type I Receptor, Transforming Growth Factor-beta Type II Receptors, Transforming Growth Factor beta/metabolism Signal Transduction Transfection Transforming Growth Factor beta/metabolism
Chemicals
Phosphorus Radioisotopes Receptors, Transforming Growth Factor beta Transforming Growth Factor beta Receptor Protein-Tyrosine Kinases Protein Serine-Threonine Kinases Receptor, Transforming Growth Factor-beta Type I Receptor, Transforming Growth Factor-beta Type II
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wrana J L
Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
Attisano L
Wieser R
Ventura F
Massagué J
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1994-08-04
Pages
341-7
Language
English
Region
England
NLM ID
0410462
Subset
IM
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