Jan 1, 1994

Hepatic transcriptional up-regulator of the rat microsomal epoxide hydrolase gene

DNA and Cell Biology
S KondoK Itakura

Abstract

Rat microsomal epoxide hydrolase (mEH) is one of the detoxification enzymes and selectively expressed in liver. A 350-bp DNA fragment of the proximal promoter was found to contain information sufficient to express the mEH gene in hepatoma cells, however not in nonhepatoma cells. We identified two cis-acting elements, epoxide hydrolase proximal element 1 (EHP1) and 2 (EHP2), in this promoter region by using transient transfection assays. Each element is a new cell-type-specific transcriptional up-regulator. The cell-type-specific activity of EHP1 correlates to the limited cell distribution of its cognate transacting factor(s). In the case of EHP2, a similar or possibly the same cognate factor(s) binding to EHP2 was detected by DNase I footprinting and gel retardation assays in both hepatoma and nonhepatoma cells. However, EHP2 functions as an up-regulator only in hepatoma cells. Our finding adds repertoire to a battery of cis-regulatory elements that are required for liver-specific transcription.

Mentioned in this Paper

Deoxyribonuclease I
Transfection
Enzymes, antithrombotic
Transcription, Genetic
Liver Carcinoma
Hepatic
Promoter
Metabolic Detoxication, Drug
Microsomes, Liver
Epoxide hydrolase

About this Paper

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