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SNIP1 is a candidate modifier of the transcriptional activity of c-Myc on E box-dependent target genes.
Fujii, Makiko; Lyakh, Lyudmila A; Bracken, Cameron P; Fukuoka, Junya; Hayakawa, Morisada; Tsukiyama, Tadasuke; Soll, Steven J; Harris, Melissa; Rocha, Sonia; Roche, Kevin C; Tominaga, Shin-Ichi; Jen, Jin; Perkins, Neil D; Lechleider, Robert J; Roberts, Anita B.
Affiliation
  • Fujii M; Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892; Department of Biochemistry, Jichi Medical University, Tochigi 329-0498, Japan. Electronic address: fujiim@jichi.ac.jp.
  • Lyakh LA; Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892.
  • Bracken CP; Division of Gene Regulation and Expression, College of Life Sciences, University of Dundee, MSI/WTB Complex, Dow Street, Dundee, DD1 5EH, United Kingdom.
  • Fukuoka J; Laboratory of Population Genetics, National Cancer Institute, Building 41, Room D702, Bethesda, Maryland 20892.
  • Hayakawa M; Department of Biochemistry, Jichi Medical University, Tochigi 329-0498, Japan.
  • Tsukiyama T; Cancer and Developmental Biology Laboratory, National Cancer Institute at Frederick, Frederick, Maryland 21702.
  • Soll SJ; Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892.
  • Harris M; Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892.
  • Rocha S; Division of Gene Regulation and Expression, College of Life Sciences, University of Dundee, MSI/WTB Complex, Dow Street, Dundee, DD1 5EH, United Kingdom.
  • Roche KC; Division of Gene Regulation and Expression, College of Life Sciences, University of Dundee, MSI/WTB Complex, Dow Street, Dundee, DD1 5EH, United Kingdom.
  • Tominaga SI; Department of Biochemistry, Jichi Medical University, Tochigi 329-0498, Japan.
  • Jen J; Laboratory of Population Genetics, National Cancer Institute, Building 41, Room D702, Bethesda, Maryland 20892.
  • Perkins ND; Division of Gene Regulation and Expression, College of Life Sciences, University of Dundee, MSI/WTB Complex, Dow Street, Dundee, DD1 5EH, United Kingdom.
  • Lechleider RJ; Molecular Oncology Research Unit, National Cancer Institute, 10/12N226, Bethesda, Maryland 20892. Electronic address: lechleiderr@mail.nih.gov.
  • Roberts AB; Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892.
Mol Cell ; 24(5): 771-783, 2006 Dec 08.
Article in En | MEDLINE | ID: mdl-17157259
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription, Genetic / Proto-Oncogene Proteins c-myc / Promoter Regions, Genetic / Carcinoma, Non-Small-Cell Lung / Intracellular Signaling Peptides and Proteins Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2006 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription, Genetic / Proto-Oncogene Proteins c-myc / Promoter Regions, Genetic / Carcinoma, Non-Small-Cell Lung / Intracellular Signaling Peptides and Proteins Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2006 Document type: Article