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Drug Metabolism and Disposition Fast Forward
First published on June 9, 2008; DOI: 10.1124/dmd.108.022020


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Received for publication April 23, 2008.
Revised June 4, 2008.
Accepted for publication June 4, 2008.

mRNA Distribution and Heterologous Expression of Orphan Cytochrome P450 20A1

Katarina Stark 1, Zhong-Liu Wu 1, Cheryl J. Bartleson 1, F. Peter Guengerich 1*

1 Vanderbilt University School of Medicine

* Address correspondence to: E-mail: f.guengerich{at}vanderbilt.edu

Abstract

Cytochrome P450 (P450) 20A1 is one of the so-called "orphan" P450s without assigned biological function. mRNA expression was detected in human liver and extrahepatic expression was noted in several human brain regions, including substantia nigra, hippocampus, and amygdala, using conventional polymerase chain reaction and RNA dot blot analysis. Adult human liver contained 3-fold higher overall mRNA levels than whole brain, although specific regions (i.e., hippocampus and substantia nigra) exhibited higher mRNA expression levels than liver. Orthologous full-length and truncated transcripts of P450 20A1 were transcribed and sequenced from rat liver, heart, and brain. In rat, the concentrations of full-length transcripts were 3-4 fold higher in brain and heart than liver. In situ hybridization of rat whole brain sections showed a similar mRNA expression pattern as observed for human P450 20A1, indicating expression in substantia nigra, hippocampus, and amygdala. A number of N-terminal modifications of the codon-optimized human P450 20A1 sequence were prepared and expressed in Escherichia coli, and two of the truncated derivatives showed characteristic P450 spectra (200-280 nmol P450/l). Although the recombinant enzyme system oxidized NADPH, no catalytic activity was observed with the heterologously expressed protein when a number of potential steroids and biogenic amines were surveyed as potential substrates. The function of P450 20A1 remains unknown; however, the sites of mRNA expression in human brain and the conservation among species may suggest possible neurophysiological function.


Key words: CYP cloning, CYP expression, cytochrome P450, cytochrome P450 function, cytochrome P450 isoforms, cytochrome P450 regulation





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