Abstract
The homeobox protein STF-1 appears to function as a master control switch for expression of the pancreatic program during development. Here we characterize a composite enhancer which directs STF-1 expression to pancreatic islet cells via two functional elements that recognize the nuclear factors HNF-3beta and BETA-2. In keeping with their inhibitory effects on islet cell maturation, glucocorticoids were found to repress STF-1 gene expression by interfering with HNF-3beta activity on the islet-specific enhancer. Overexpression of HNF-3beta suppressed glucocorticoid receptor-mediated inhibition of the STF-1 gene, and our results suggest that the expansion of pancreatic islet precursor cells during development may be restricted by hormonal cues which regulate STF-1 gene expression.
MeSH Terms
Animals
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Blotting, Northern
Blotting, Western
COS Cells
DNA Footprinting
DNA-Binding Proteins/genetics,metabolism
Gene Expression Regulation
Glucocorticoids/pharmacology
HeLa Cells
Helix-Loop-Helix Motifs
Hepatocyte Nuclear Factor 3-beta
Homeodomain Proteins/genetics,metabolism
Humans
Islets of Langerhans/metabolism
Molecular Sequence Data
Nuclear Proteins/genetics,metabolism
Trans-Activators/genetics,metabolism
Transcription Factors/genetics,metabolism
Transfection
Chemicals
Basic Helix-Loop-Helix Transcription Factors
DNA-Binding Proteins
FOXA2 protein, human
Glucocorticoids
Homeodomain Proteins
NEUROD1 protein, human
Nuclear Proteins
Trans-Activators
Transcription Factors
pancreatic and duodenal homeobox 1 protein
Hepatocyte Nuclear Factor 3-beta
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sharma S
Department of Biology, University of California, San Diego, La Jolla 92037, USA.
Jhala U S
Johnson T
Ferreri K
Leonard J
Montminy M
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