Genetics, Vol. 152, 1653-1667, August 1999, Copyright © 1999

Analysis of the Doublesex Female Protein in Drosophila melanogaster: Role in Sexual Differentiation and Behavior and Dependence on Intersex

Julie A. Waterburya, Larry L. Jacksonb, and Paul Schedla
a Department of Molecular Biology, Princeton University, Princeton, New Jersey, 08544
b Chemistry and Biochemistry Department, Montana State University, Bozeman, Montana 59717-0310

Corresponding author: Paul Schedl, Department of Molecular Biology, Princeton University, Princeton, NJ 08544., pschedl{at}molbio.princeton.edu (E-mail)

Communicating editor: K. ANDERSON

doublesex (dsx) is unusual among the known sex-determination genes of Drosophila melanogaster in that functional homologs are found in distantly related species. In flies, dsx occupies a position near the bottom of the sex determination hierarchy. It is expressed in male- and female-specific forms and these proteins function as sex-specific transcription factors. In the studies reported here, we have ectopically expressed the female Dsx protein (DsxF) from a constitutive promoter and examined its regulatory activities independent of other upstream factors involved in female sex determination. We show that it functions as a positive regulator of female differentiation and a negative regulator of male differentiation. As predicted by the DNA-binding properties of the Dsx protein, DsxF and DsxM compete with each other for the regulation of target genes. In addition to directing sex-specific differentiation, DsxF plays an important role in sexual behavior. Wild-type males ectopically expressing DsxF are actively courted by other males. This acquisition of feminine sex appeal is likely due to the induction of female pheromones by DsxF. More extreme behavioral abnormalities are observed when DsxF is ectopically expressed in dsx- XY animals; these animals are not only courted by, but also copulate with, wild-type males. Finally, we provide evidence that intersex is required for the feminizing activities of DsxF and that it is not regulated by the sex-specific splicing cascade.





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