The role of tonicity responsive enhancer sites in the transcriptional regulation of human hsp70-2 in response to hypertonic stress.
- Author:
Jee In HEO
1
;
Mi Suk LEE
;
Jeong Hyun KIM
;
Jae Seon LEE
;
Jaebong KIM
;
Jae Bong PARK
;
Jae Yong LEE
;
Jeong A HAN
;
Jong Il KIM
Author Information
1. Department of Biochemistry, Hallym University College of Medicine, Chuncheon 200-702, Korea. jongil@hallym.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
HSP70 heat-shock proteins;
heat-shock proteins;
stress;
transcription factors;
gene expression regulation
- MeSH:
Transcription, Genetic/drug effects/genetics;
Transcription Factors/genetics/*physiology;
Saline Solution, Hypertonic/*pharmacology;
Reverse Transcriptase Polymerase Chain Reaction;
Protein Binding;
Promoter Regions (Genetics)/genetics;
Point Mutation;
Mutagenesis, Site-Directed;
Humans;
HSP70 Heat-Shock Proteins/*genetics/metabolism;
Gene Expression Regulation/*drug effects;
DNA-Binding Proteins/genetics/metabolism;
Cell Line;
Binding Sites/genetics;
Base Sequence;
5' Flanking Region/genetics
- From:Experimental & Molecular Medicine
2006;38(3):295-301
- CountryRepublic of Korea
- Language:English
-
Abstract:
The inducible 70 kDa heat shock proteins (Hsp70) in mice are encoded by two almost identical genes, hsp70.1 and hsp70.3. Studies have found that only hsp70.1 is induced by hypertonic stress while both hsp70.1 and hsp70.3 genes are expressed in response to heat shock stress. It is unclear if the human counterparts, hsp70-2 and hsp70-1, are differentially regulated by heat shock and osmotic stress. This study found that only hsp70-2 was induced by hypertonic stress in human embryonic kidney epithelial cells and fibroblasts, while heat shock stress induced both hsp70-1 and hsp70-2. The human hsp70-2 promoter region contains three TonE (tonicity-responsive enhancer) sites, which were reported to play an important role in the response to hypertonicity. When the reporter plasmids containing different parts of the 5' flanking region of hsp70-2 were transfected into human embryonic kidney epithelial cells or fibroblasts, one TonE site at -135 was found to play a key role in the response to hypertonicity. The inactivation of the TonE site using site-directed mutagenesis led to the complete loss of induction by hypertonicity, which demonstrates the essential role of the TonE site. This suggests that the TonE site and the TonEBP (TonE binding protein) are the major regulators for the cellular response against high osmolarity in human kidney tissue.
