Biliverdin Reductase, a Novel Regulator for Induction of Activating Transcription Factor-2 and Heme Oxygenase-1

Anatoliy Kravets, Zhenbo Hu, Tihomir Miralem, Michael D. Torno, Mahin D. Maines
2004 Journal of Biological Chemistry  
Biliverdin IX␣ reductase (BVR) catalyzes reduction of the HO activity product, biliverdin, to bilirubin. hBVR is a serine/threonine kinase that contains a bZip domain. Presently, regulation of gene expression by hBVR was examined. 293A cells were infected with adenovirusdoxycycline (Ad-Dox)-inducible hBVR cDNA. High level expression of hBVR was determined at mRNA, protein, and activity levels 8 h after induction. Cell signal transduction microarray analysis of cells infected with expression or
more » ... ith the control Ad-inverted (INV)-hBVR vector identified ATF-2 among several up-regulated genes. ATF-2 is a bZip transcription factor for activation of cAMP response element (CRE) and a dimeric partner to c-jun in MAPK pathway that regulates the stress protein, HO-1, expression. Northern and Western blot analyses showed increases of ϳ10-fold in ATF-2 mRNA and protein at 16 and 24 h after Dox addition. Ad-INV-hBVR did not effect ATF-2 expression. In hBVR-infected cells, levels of HO-1 mRNA and protein were increased. In vitro translated hBVR and nuclear extract containing hBVR in gel mobility-shift assay bound to AP-1 sites in the ATF-2 promoter region and to an oligonucleotide containing the CRE site. Both bindings could be competed out by excess unlabeled probe; in the presence of hBVR antibody, they displayed shifted bands. Co-transfection of hBVR with ATF-2 or c-jun promoters caused a severalfold increase in luciferase activity. hBVR modulation of ATF-2 and HO-1 expression suggests it has a potential role in regulation of AP-1 and cAMP-regulated genes and a role in cell signaling. We propose that increased expression of the protein can be used to alter the gene expression profile in the cell. The well known function of biliverdin IX␣ reductase (BVR) 1 is catalysis of biliverdin reduction to bilirubin (1-8). Biliverdin is a product of cleavage of the heme macrocycle (Fe-protoporphyrin IX, hemin, and heme b) by the microsomal enzyme heme oxygenase (HO) system (reviewed in Refs. 9 -11). The enzymes are also known as the heat shock protein-32 (HSP32) family of proteins (12-16).
doi:10.1074/jbc.m314251200 pmid:14988408 fatcat:7scrmpqstbg2pc4e2gd6ll4qw4