Your browser doesn't support javascript.
loading
Insulin Receptor Associates with Promoters Genome-wide and Regulates Gene Expression.
Hancock, Melissa L; Meyer, Rebecca C; Mistry, Meeta; Khetani, Radhika S; Wagschal, Alexandre; Shin, Taehwan; Ho Sui, Shannan J; Näär, Anders M; Flanagan, John G.
Afiliación
  • Hancock ML; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
  • Meyer RC; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
  • Mistry M; Bioinformatics Core, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
  • Khetani RS; Bioinformatics Core, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
  • Wagschal A; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Massachusetts General Hospital Cancer Center, Charlestown, MA 02129, USA.
  • Shin T; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
  • Ho Sui SJ; Bioinformatics Core, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
  • Näär AM; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Massachusetts General Hospital Cancer Center, Charlestown, MA 02129, USA.
  • Flanagan JG; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Program in Neuroscience, Harvard Medical School, Boston, MA 02115, USA. Electronic address: flanagan@hms.harvard.edu.
Cell ; 177(3): 722-736.e22, 2019 04 18.
Article en En | MEDLINE | ID: mdl-30955890
ABSTRACT
Insulin receptor (IR) signaling is central to normal metabolic control and dysregulated in prevalent chronic diseases. IR binds insulin at the cell surface and transduces rapid signaling via cytoplasmic kinases. However, mechanisms mediating long-term effects of insulin remain unclear. Here, we show that IR associates with RNA polymerase II in the nucleus, with striking enrichment at promoters genome-wide. The target genes were highly enriched for insulin-related functions including lipid metabolism and protein synthesis and diseases including diabetes, neurodegeneration, and cancer. IR chromatin binding was increased by insulin and impaired in an insulin-resistant disease model. Promoter binding by IR was mediated by coregulator host cell factor-1 (HCF-1) and transcription factors, revealing an HCF-1-dependent pathway for gene regulation by insulin. These results show that IR interacts with transcriptional machinery at promoters and identify a pathway regulating genes linked to insulin's effects in physiology and disease.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Receptor de Insulina / Regulación de la Expresión Génica / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans / Male Idioma: En Revista: Cell Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Receptor de Insulina / Regulación de la Expresión Génica / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans / Male Idioma: En Revista: Cell Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos