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Originally published In Press as doi:10.1074/jbc.M510293200 on February 7, 2006

J. Biol. Chem., Vol. 281, Issue 14, 9205-9209, April 7, 2006
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The Role of Drosophila ninaG Oxidoreductase in Visual Pigment Chromophore Biogenesis*

Syed Tariq Ahmad{ddagger}, Michelle V. Joyce§, Bill Boggess§, and Joseph E. O'Tousa{ddagger}1

From the {ddagger}Department of Biological Sciences, and §Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556

We previously reported (Sarfare, S., Ahmad, S. T., Joyce, M. V., Boggess, B., and O'Tousa, J. E. (2005) J. Biol. Chem. 280, 11895–11901) that the Drosophila ninaG gene encodes an oxidoreductase involved in the biosynthesis of the (3S)-3-hydroxyretinal serving as chromophore for Rh1 rhodopsin and that ninaG mutant flies expressing Rh4 as the major opsin accumulate large amounts of a different retinoid. Here, we show that this unknown retinoid is 11-cis-3-hydroxyretinol. Reversed phase high performance liquid chromatography coupled with a photodiode array UV-visible absorbance detector and mass spectrometer revealed a major product eluting at a retention time, tr, of 3.5 min with a {lambda}max of ~324 nm and with a base peak in the mass spectrum at m/z 285. These observations are identical with those of the 3-hydroxyretinol standard. The base peak in the electrospray ionization mass spectrum arises from the loss of a water molecule from the protonated molecule at m/z 303 because of fragmentation in the ion source. These results suggest that 11-cis-3-hydroxyretinol is an intermediate required for chromophore biogenesis in Drosophila. We further show that ninaG mutants fed on retinal as the sole source of vitamin A are able to synthesize 3-hydroxyretinoids. Thus, the NinaG oxidoreductase is not responsible for the initial hydroxylation of the retinal ring but rather acts in a subsequent step in chromophore production. These data are used to review chromophore biosynthesis and propose that NinaG acts in the conversion of (3R)-3-hydroxyretinol to the 3S enantiomer.


Received for publication, September 19, 2005 , and in revised form, December 29, 2005.

* The work was supported by National Institutes of Health Grant EY06808. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1 To whom correspondence should be addressed. Tel.: 574-631-6093; Fax: 574-631-7413; E-mail: jotousa{at}nd.edu.


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