HNF1 and/or HNF3 may contribute to the tissue specific expression of glucokinase gene.
- Author:
Ji Young CHA
1
;
Ha Il KIM
;
Seung Soon IM
;
Tian Zhu LI
;
Yong Ho AHN
Author Information
1. Dept. of Biochemistry and Molecular Biology and the Institute of Genetic Science, College of Medicine, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
GK;
GLUT2;
HNF1;
HNF3
- MeSH:
3T3 Cells;
Animal;
Blotting, Northern;
Cell Line;
Cell Nucleus/metabolism;
Cells, Cultured;
DNA-Binding Proteins/genetics/*physiology;
Genes, Reporter;
Glucokinase/*biosynthesis/*genetics;
Hela Cells;
Human;
Liver/metabolism;
Luciferase/metabolism;
Mice;
Models, Genetic;
Nuclear Proteins/genetics/*physiology;
Plasmids/metabolism;
Promoter Regions (Genetics);
Protein Binding;
Rats;
Support, Non-U.S. Gov't;
Tissue Distribution;
Transcription Factors/genetics/*physiology;
Transcription, Genetic;
Transfection
- From:Experimental & Molecular Medicine
2001;33(2):59-63
- CountryRepublic of Korea
- Language:English
-
Abstract:
A possible role of hepatocyte nuclear factor 1 (HNF1) or HNF3, a predominant trans-acting factors of hepatic or pancreatic beta-cells, was examined on the tissue specific interdependent expression of glucokinase (GK) in liver, H4IIE, HepG2, HIT-T15 and MIN6 cell line. The tissues or cell lines known to express GK showed abundant levels of HNF1 and HNF3 mRNA as observed in liver, H4IIE, HepG2, HIT-T15 and MIN6 cells, whereas they were not detected in brain, heart, NIH 3T3, HeLa cells. The promoter of glucokinase contains several HNF3 consensus sequences and are well conserved in human, mouse and rat. Transfection of the glucokinase promotor linked with luciferase reporter to liver or pancreatic beta cell lines showed high interacting activities with HNF1 and HNF3, whereas minimal activities were detected in the cells expressing very low levels of HNFs. The binding of HNF1 or HNF3 to the GK promoter genes was confirmed by electrophoretic mobility shift assay (EMSA). From these data, we propose that the expression of HNF1 and/or HNF3 may, in part, contribute to the tissue specific expression of GK.
