Abstract

Molecular characterization of male and female rat liver aldehyde oxidase is reported. As described for the mouse liver, male and female rat liver expressed kinetically distinct forms of aldehyde oxidase. Our data suggest that the two forms arise as a result of differences in redox state and are most simply explained by expression of a single gene encoding aldehyde oxidase in rats. In support of this argument we have sequenced cDNAs from male and female rat liver. We examined mRNA expression by Northern blot analysis with RNA from males and females, from several tissues, and following androgen induction. Purified rat liver enzyme from males or females revealed a single 150-kDa species consistent with cDNA sequence analysis. Both male and female forms were reactive to the same carboxyl-terminal directed antisera. Km(app) values obtained in crude extracts of male or female rat liver and post-benzamidine-purified aldehyde oxidase differed substantially from each other but could be interconverted by chemical reduction with dithiothreitol or oxidation with 4,4'-dithiodipyridine. Our data indicate that a single gene is most likely expressed in male or female rat liver and that the kinetic differences between male and female rat liver aldehyde oxidases are sensitive to redox manipulation.

Highlights

  • Molecular characterization of male and female rat liver aldehyde oxidase is reported

  • We examined expression of Aldehyde oxidase (AOX) by Northern blot analysis from males and females, from several tissues, and have examined the effect of androgen regulation

  • The rat AOXs clearly belong to the molybdenum iron-sulfur flavoproteins that include AOX, xanthine dehydrogenase (XDH), and XO

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Summary

Introduction

Molecular characterization of male and female rat liver aldehyde oxidase is reported. Our data suggest that the two forms arise as a result of differences in redox state and are most explained by expression of a single gene encoding aldehyde oxidase in rats In support of this argument we have sequenced cDNAs from male and female rat liver. Purified rat liver enzyme from males or females revealed a single 150-kDa species consistent with cDNA sequence analysis Both male and female forms were reactive to the same carboxyl-terminal directed antisera. Previous work had shown that castration resulted in the loss of a male pattern with conversion to a female pattern and TP supplementation restored the male-specific pattern of AOX expression (9) This observation was consistent with early reports of androgenic regulation of mouse hepatic AOX (10, 11). How the differences between male and female hepatic AOXs were generated remained unclear

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