The quemao (qm) locus of Drosophila melanogaster is characterized by a
P-element-associated mutant lacking most of the large bristles on the
thorax and by several EMS-induced recessive lethals. quemao was clone
d using a transposon tagging strategy. P-element-mediated transformati
on demonstrated that the cloned qm DNA sequence (from the 65F cytologi
cal region) rescues the mutant phenotype. A 2.3-kb qm transcript was i
dentified by Northern blot analysis by sequencing of the isolated qm c
DNA clones and by 5' rapid amplification cDNA end (RACE). The predicte
d amino acid sequence (338 residues) of the coding region of the qm tr
anscript shares 42, 31, 13, 20, and 12% identical amino acid sequences
with the geranylgeranyl pyrophosphate synthase (GGPPS) of fungi, yeas
t, plants, archaebacteria, and eubacteria, respectively. It also conta
ins five highly conserved domains common among all known isoprenyl pyr
ophosphate synthases. The P element associated with the original qm mu
tant is inserted in the 5' untranslated region of the transcript. An E
MS-induced qm nonsense mutation at the 12th codon leads to recessive l
ethality at the first larval instar, indicating the essential role of
qm in the isoprenoid biosynthesis of insects.