Transcription of the Human Microsomal Epoxide Hydrolase Gene (EPHX1) Is Regulated by PARP-1 and Histone H1.2. Association with Sodium-Dependent Bile Acid Transport

• Published in: PloS one Vol. 10; no. 5; p. e0125318
• Main Authors: Peng, Hui, Zhu, Qin-shi, Zhong, Shuping, Levy, Daniel
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 20.05.2015; Public Library of Science (PLoS)
• Subjects: Acids; Adenosine diphosphate; Base Sequence; Bile; Bile acid metabolism; Bile acids; Bile Acids and Salts - metabolism; Biological Transport - genetics; Care and treatment; Cell Line, Tumor; Cellular signal transduction; Cholesterol; Defects; Diagnosis; Epoxide hydrolase; Epoxide Hydrolases - genetics; Epoxide Hydrolases - metabolism; Epoxy compounds; Excretion; Gene expression; Gene Expression Regulation; Gene polymorphism; Gene regulation; Hep G2 Cells; Hepatocytes; Hepatocytes - metabolism; Histone H1; Histones - metabolism; Homeostasis; Homology; Humans; Introns - genetics; Liver; Liver diseases; Mass spectrometry; Mass spectroscopy; Metabolism; Molecular Sequence Data; Mutation; Nuclear receptors; Nucleosomes - genetics; Oligonucleotides; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) polymerase; Poly(ADP-ribose) Polymerases - genetics; Poly(ADP-ribose) Polymerases - metabolism; Polymorphism; Polymorphism, Genetic - genetics; Promoter Regions, Genetic - genetics; Protein binding; Proteins; Receptors; Regulatory proteins; Retinoid X receptors; Ribose; Risk factors; Rodents; Signal transduction; Signaling; Sodium; Sodium - metabolism; Transcription; Transcription, Genetic - genetics; Transport; Xenobiotics
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0125318

Microsomal epoxide hydrolase (mEH) is a bifunctional protein that plays a central role in the metabolism of numerous xenobiotics as well as mediating the sodium-dependent transport of bile acids into hepatocytes. These compounds are involved in cholesterol homeostasis, lipid digestion, excretion of xenobiotics and the regulation of several nuclear receptors and signaling transduction pathways. Previous studies have demonstrated the critical role of GATA-4, a C/EBPα-NF/Y complex and an HNF-4α/CAR/RXR/PSF complex in the transcriptional regulation of the mEH gene (EPHX1). Studies also identified heterozygous mutations in human EPHX1 that resulted in a 95% decrease in mEH expression levels which was associated with a decrease in bile acid transport and severe hypercholanemia. In the present investigation we demonstrate that EPHX1 transcription is significantly inhibited by two heterozygous mutations observed in the Old Order Amish population that present numerous hypercholanemic subjects in the absence of liver damage suggesting a defect in bile acid transport into the hepatocyte. The identity of the regulatory proteins binding to these sites, established using biotinylated oligonucleotides in conjunction with mass spectrometry was shown to be poly(ADP-ribose)polymerase-1 (PARP-1) bound to the EPHX1 proximal promoter and a linker histone complex, H1.2/Aly, bound to a regulatory intron 1 site. These sites exhibited 71% homology and may represent potential nucleosome positioning domains. The high frequency of the H1.2 site polymorphism in the Amish population results in a potential genetic predisposition to hypercholanemia and in conjunction with our previous studies, further supports the critical role of mEH in mediating bile acid transport into hepatocytes.