Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-9688
Proc Natl Acad Sci U S A. January 30, 2001; 98 (3): 974-9.

Regulation of Smad degradation and activity by Smurf2, an E3 ubiquitin ligase.

Zhang Y , Chang C , Gehling DJ , Hemmati-Brivanlou A , Derynck R .


Abstract
Smad proteins are key intracellular signaling effectors for the transforming growth factor-beta superfamily of peptide growth factors. Following receptor-induced activation, Smads move into the nucleus to activate transcription of a select set of target genes. The activity of Smad proteins must be tightly regulated to exert the biological effects of different ligands in a timely manner. Here, we report the identification of Smurf2, a new member of the Hect family of E3 ubiquitin ligases. Smurf2 selectively interacts with receptor-regulated Smads and preferentially targets Smad1 for ubiquitination and proteasome-mediated degradation. At higher expression levels, Smurf2 also decreases the protein levels of Smad2, but not Smad3. In Xenopus embryos, ectopic Smurf2 expression specifically inhibits Smad1 responses and thereby affects embryonic patterning by bone morphogenetic protein signals. These findings suggest that Smurf2 may regulate the competence of a cell to respond to transforming growth factor-beta/bone morphogenetic protein signaling through a distinct degradation pathway that is similar to, yet independent of, Smurf1.

PubMed ID: 11158580
PMC ID: PMC14694
Article link: Proc Natl Acad Sci U S A.
Grant support: CA63101 NCI NIH HHS , CA63101 NCI NIH HHS , CA63101 NCI NIH HHS , CA63101 NCI NIH HHS , CA63101 NCI NIH HHS , CA63101 NCI NIH HHS , HD32105 NICHD NIH HHS

Genes referenced: smad1 smad2 smad3 smurf1 smurf2
Antibodies referenced:

My Xenbase: [ Log-in / Register ]
version: [3.2.1]


Major funding for Xenbase is provided by the National Institute of Child Health and Human Development, grant P41 HD064556