| Literature DB >> 17157259 |
Makiko Fujii1, Lyudmila A Lyakh2, Cameron P Bracken3, Junya Fukuoka4, Morisada Hayakawa5, Tadasuke Tsukiyama6, Steven J Soll2, Melissa Harris2, Sonia Rocha3, Kevin C Roche3, Shin-Ichi Tominaga5, Jin Jen4, Neil D Perkins3, Robert J Lechleider7, Anita B Roberts2.
Abstract
Using a yeast two-hybrid screen, we found that SNIP1 (Smad nuclear-interacting protein 1) associates with c-Myc, a key regulator of cell proliferation and transformation. We demonstrate that SNIP1 functions as an important regulator of c-Myc activity, binding the N terminus of c-Myc through its own C terminus, and that SNIP1 enhances the transcriptional activity of c-Myc both by stabilizing it against proteosomal degradation and by bridging the c-Myc/p300 complex. These effects of SNIP1 on c-Myc likely contribute to synergistic effects of SNIP1, c-Myc, and H-Ras in inducing formation of foci in an in vitro transformation assay and also in supporting anchorage-independent growth. The significant association of SNIP1 and c-Myc staining in a non-small cell lung cancer tissue array is further evidence that their activities might be linked and suggests that SNIP1 might be an important modulator of c-Myc activity in carcinogenesis.Entities:
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Year: 2006 PMID: 17157259 DOI: 10.1016/j.molcel.2006.11.006
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970