Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Sci. Signal., 10 June 2008
Vol. 1, Issue 23, p. ec213
[DOI: 10.1126/scisignal.123ec213]


Posttranslational Modifications Sumoylating TGF-β Receptors

Nancy R. Gough

Science Signaling, AAAS, Washington, DC 20005, USA

Signaling by the transforming growth factor-β (TGF-β) superfamily is important in development and in adult tissues, and alterations in this pathway may contribute to some types of cancers and metastasis. Kang et al. provide evidence from in vitro experiments and from transfected cells that the type I subunit of the TGF-β receptor (TβRI) is modified by addition of the small molecule SUMO (see commentary by Miyazono et al.). Mutation analysis suggested that Lys389 was the target for sumoylation. Phosphorylation of the TβRI, which is stimulated in response to ligand binding to the dimeric TβRI and TβRII complex, was necessary for SUMO modification because kinase-inactivated forms of a TβRI and TβRII chimera were not sumoylated in vitro or in transfected cells, and sumoylation was not detected in vitro if the reaction was carried out in the presence of a phosphatase. SUMO modification was detected most readily with an activated mutant of TβRI (caTβRI); moreover, in cells coexpressing caTβRI, SUMO-conjugating enzymes, tagged SUMO, and a mutant Smad3, the interaction between the receptor and Smad3 was enhanced (based on coimmunoprecipitation) compared to that in cells only expressing caTβRI and the mutant Smad3. Expression in Tgfbr1/– cells of a Lys389 mutant TβRI that was not sumoylated resulted in less activation of Smads and less activation of TGF-β target genes (either endogenous targets or reporter genes) than did expression of the wild-type receptor, suggesting that sumoylation enhances TGF-β signaling. Ras-transformed mouse embryo fibroblasts from Tgfbr1/– animals showed decreased invasiveness in a cell migration assay and formed smaller and fewer metastatic tumor nodules when injected into mice when expressing the Lys389 mutant TβRI than when expressing the wild-type receptor. Introduction of a mutation (Ser387Tyr) found in some human cancers resulted in a sumoylation-defective form of the receptor; however, in the tumor-metastasis model with Ras-transformed cells expressing this mutant form of the receptor, these cells formed fewer and smaller metastatic nodules than did cells expressing wild-type receptors. Thus, mechanisms by which TGF-β signaling contributes to cancer are complex.

J. S. Kang, E. F. Saunier, R. J. Akhurst, R. Derynck, The type I TGF-β receptor is covalently modified and regulated by sumoylation. Nat. Cell Biol. 10, 654-664 (2008). [PubMed]

K. Miyazono, Y. Kamiya, K. Miyazawa, SUMO amplifies TGF-β signalling. Nat. Cell Biol. 10, 635-637 (2008). [PubMed]

Citation: N. R. Gough, Sumoylating TGF-β Receptors. Sci. Signal. 1, ec213 (2008).

To Advertise     Find Products

Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882