학술논문

Insulin Receptor Associates with Promoters Genome-wide and Regulates Gene Expression
Document Type
article
Source
Cell. 177(3)
Subject
Genetics
Human Genome
Diabetes
1.1 Normal biological development and functioning
Aetiology
2.1 Biological and endogenous factors
Underpinning research
Metabolic and endocrine
Generic health relevance
Good Health and Well Being
Animals
Cell Line
Tumor
Chromatin
Gene Expression Regulation
Genome-Wide Association Study
Host Cell Factor C1
Humans
Insulin
Liver
Male
Mice
Mice
Inbred C57BL
Promoter Regions
Genetic
Protein Binding
Protein Subunits
RNA Interference
RNA Polymerase II
RNA
Small Interfering
Receptor
Insulin
Signal Transduction
HCFC1
INSR
RNA polymerase II
coregulator host cell factor-1
gene promoter
insulin receptor signaling
nuclear receptor tyrosine kinase
transcription factor
Biological Sciences
Medical and Health Sciences
Developmental Biology
Language
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.