PUBLICATION

FOXN3 Regulates Hepatic Glucose Utilization

Authors
Karanth, S., Zinkhan, E.K., Hill, J.T., Yost, H.J., Schlegel, A.
ID
ZDB-PUB-160614-8
Date
2016
Source
Cell Reports   15(12): 2745-55 (Journal)
Registered Authors
Karanth, Santhosh, Schlegel, Amnon, Yost, H. Joseph
Keywords
none
Datasets
GEO:GSE80003
MeSH Terms
  • Alleles
  • Animals
  • Blood Glucose/metabolism
  • Down-Regulation/genetics
  • Fasting/blood
  • Glucose/metabolism*
  • Glycolysis/genetics
  • Hep G2 Cells
  • Humans
  • Liver/metabolism*
  • Male
  • Models, Biological
  • Polymorphism, Single Nucleotide/genetics
  • Proto-Oncogene Proteins c-myc/metabolism
  • Rats
  • Repressor Proteins/genetics
  • Repressor Proteins/metabolism*
  • Risk Factors
  • Zebrafish
PubMed
27292639 Full text @ Cell Rep.
Abstract
A SNP (rs8004664) in the first intron of the FOXN3 gene is associated with human fasting blood glucose. We find that carriers of the risk allele have higher hepatic expression of the transcriptional repressor FOXN3. Rat Foxn3 protein and zebrafish foxn3 transcripts are downregulated during fasting, a process recapitulated in human HepG2 hepatoma cells. Transgenic overexpression of zebrafish foxn3 or human FOXN3 increases zebrafish hepatic gluconeogenic gene expression, whole-larval free glucose, and adult fasting blood glucose and also decreases expression of glycolytic genes. Hepatic FOXN3 overexpression suppresses expression of mycb, whose ortholog MYC is known to directly stimulate expression of glucose-utilization enzymes. Carriers of the rs8004664 risk allele have decreased MYC transcript abundance. Human FOXN3 binds DNA sequences in the human MYC and zebrafish mycb loci. We conclude that the rs8004664 risk allele drives excessive expression of FOXN3 during fasting and that FOXN3 regulates fasting blood glucose.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping