Nucleoprotein complexes that regulate gene expression in adipocyte differentiation: direct participation of c-fos

Robert J. Distel, Hyo Sung Ro, Barry S. Rosen, Douglas L. Groves, Bruce M. Spiegelman

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409 Citas (Scopus)

Resumen

Adipocyte differentiation is accompanied by the transcriptional activation of many new genes, including a putative lipid-binding protein termed adipocyte P2 (aP2). The aP2 gene contains a regulatory element (FSE2) 124 bases 5′ to its start of transcription. This element binds nuclear factors in sequence-specific and differentiation-dependent fashion as determined by altered mobility in gel retardation assays. Deletion analysis of promoter-linked transfection assays and competition of these constructions in cells with a synthetic FSE2 element suggest that trans-acting factors bind to this region and act as negative regulators of aP2 gene activity in preadipocytes. c-fos appears to participate directly in this nucleoprotein complex, as demonstrated by the ability of antibodies to c-fos to disrupt specific binding of factors to the FSE2 sequence but not to factor-binding sequences from several other genes. Antibodies to c-fos specifically immunoprecipitate protein complexes covalently bound to FSE2 DNA via UV cross-linking.

Idioma originalEnglish
Páginas (desde-hasta)835-844
Número de páginas10
PublicaciónCell
Volumen49
N.º6
DOI
EstadoPublished - jun. 19 1987
Publicado de forma externa

Nota bibliográfica

Funding Information:
The authors thank Dr. Tom Roberts for helpful discussions and a critical review of this manuscript. We are also indebted to the following investigators for supplying antisera: Drs. Tom Curran, Dennis Slamon, Bob Eisenman, Peggy Bradley, Keigi Fujiwara, K. Sue Cook, and l-lye Yeong Min. We thank Ms. Adah Levens for expert preparation of this manuscript. This work was supported by National Institutes of Health grants AM31405 and DK34605. R. Distel is supported by NIH postdoctoral fellowship AM07715. H.-S. R. is supported by AHA (Massachusetts affiliate) postdoctoral fellowship 13-409-667.

ASJC Scopus Subject Areas

  • General Biochemistry,Genetics and Molecular Biology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

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