ABC transporters involved in transport of eye pigment precursors in Drosophila melanogaster.

Publisher Summary The usual red-brown color of the eyes of the vinegar fly Drosophila melanogaster is because of the presence of two light-screening pigments: (1) xanthommatin, which is brown and (2) a class of pigments known as drosopterins, which are red. These pigments are deposited in membrane-bound granules in specialized pigment cells in each ommatidium of the compound eye. Xanthommatin is derived biosynthetically from tryptophan and drosopterins are derived from guanosine triphosphate (GTP). The chapter characterizes the genes and proteins involved in transport of the pigment precursor molecules from the haemolymph into the fly eye pigment cells. Studies of eye color mutant flies have revealed three genetic loci (white, brown, and scarlet) in which mutations do not alter levels of the enzymes involved in pigment biosynthesis, but instead interfere with the ability of cells to take up pigment precursors.

[1]  S. Henikoff,et al.  The brown protein of Drosophila melanogaster is similar to the white protein and to components of active transport complexes , 1988, Molecular and cellular biology.

[2]  K. Summers,et al.  Biology of Eye Pigmentation in Insects , 1982 .

[3]  P. Bingham,et al.  Regulation of white locus expression: The structure of mutant alleles at the white locus of Drosophila melanogaster , 1982, Cell.

[4]  M. Azzaria,et al.  Discrete mutations introduced in the predicted nucleotide-binding sites of the mdr1 gene abolish its ability to confer multidrug resistance , 1989, Molecular and cellular biology.

[5]  T. Hazelrigg The Drosophila white gene: a molecular update , 1987 .

[6]  G M Rubin,et al.  DNA sequence of the white locus of Drosophila melanogaster. , 1984, Journal of molecular biology.

[7]  M. Bownes,et al.  Drosophila: A practical approach: edited by D. B. Roberts IRL Press, 1986. £26.00/$47.00 (xix + 295 pages) ISBN 0 94746 66 7 , 1987 .

[8]  A. E. Senior,et al.  Directed mutagenesis of the beta-subunit of F1-ATPase from Escherichia coli. , 1987, The Journal of biological chemistry.

[9]  G. Rubin,et al.  Cloning of DNA sequences from the white locus of D. melanogaster by a novel and general method , 1981, Cell.

[10]  J. L. Farmer An allele-specific suppressor of White-coral in Drosophila melanogaster , 1977, Heredity.

[11]  Stephen M. Mount,et al.  Sequence of a cDNA from the Drosophila melanogaster white gene. , 1990, Nucleic acids research.

[12]  V. Pirrotta,et al.  Microdissection and cloning of the white locus and the 3B1‐3C2 region of the Drosophila X chromosome , 1983, The EMBO journal.

[13]  C. Osgood,et al.  Molecular analysis of chemically-induced mutations at the RpII215 locus of Drosophila melanogaster. , 1986, Mutation research.

[14]  G. Cox,et al.  Specific amino acid residues in both the PstB and PstC proteins are required for phosphate transport by the Escherichia coli Pst system , 1989, Journal of bacteriology.

[15]  Paul Schedl,et al.  A position-effect assay for boundaries of higher order chromosomal domains , 1991, Cell.

[16]  D. Latchman Herpes infection and AIDS , 1987, Nature.

[17]  S. Michaelis,et al.  Mutational analysis of the yeast a‐factor transporter STE6, a member of the ATP binding cassette (ABC) protein superfamily. , 1991, The EMBO journal.

[18]  B. S. Baker,et al.  Cloning and characterization of the scarlet gene of Drosophila melanogaster. , 1989, Genetics.

[19]  R. Paro,et al.  Molecular cloning of the white locus region of Drosophila melanogaster using a large transposable element , 1982, The EMBO journal.