- THIS ARTICLE
- Full Text
- Full Text (PDF)
- Data Supplement
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Email this article to a friend
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Zhou, X.
- Articles by Riddiford, L. M.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Zhou, X.
- Articles by Riddiford, L. M.
Genetics, Vol. 178, 273-281, January 2008, Copyright © 2008
doi:10.1534/genetics.107.080754
rosy Function Is Required for Juvenile Hormone Effects in Drosophila melanogaster
Xiaofeng Zhou1 and Lynn M. Riddiford2
Department of Biology, University of Washington, Seattle, Washington 98195-1800
2 Corresponding author: Janelia Farm Research Campus, Howard Hughes Medical Institute, 19700 Helix Dr., Ashburn, VA 20147.
E-mail: riddifordl{at}janelia.hhmi.org
Application of a high dose of juvenile hormone (JH) III or its mimics (JHM) to Drosophila at the white puparium stage causes the formation of a pupal-like abdomen with few or no short bristles. We report here that the rosy (ry) gene encoding the enzyme xanthine dehydrogenase (XDH), which catalyzes the final two-step oxidation in purine catabolism, is required for this effect of JH on the epidermis. In ry506 (null allele) homozygotes or hemizygotes, JH III or pyriproxifen (a JHM) had little effect on abdominal bristle or cuticle formation, but disrupted the development of the central nervous system as in wild-type flies. Wild-type ry rescued the JH sensitivity of the abdominal epidermis in ry506 mutants. Inhibition of XDH activity phenocopied the ry null mutant's insensitivity to JH. Larvae fed on hypoxanthine or xanthine showed a decreased JH sensitivity. ry506 clones were sensitive to JH, indicating that ry is required non-cell autonomously for the JH effects. Normally JH applied at pupariation causes the aberrant reexpression of the transcription factor broad in the abdominal epidermis during adult development, but in the ry506 mutant most of the cells in the dorsal tergite showed no broad reexpression, indicating that ry is upstream of broad in the JH signaling pathway.