The enhancer of yellow 1 gene, e(y)1, of Drosophila melanogaster has been c
loned and demonstrated to encode the TAF(II)40 protein. The e(y)1 gene is e
xpressed in females much more strongly than in males due to the accumulatio
n of e(y)1 mRNA in the ovaries. Two different e(y)1 mutations have been obt
ained. The e(y)1(ul) mutation, induced by the insertion of Stalker into the
coding region, leads to the replacement of 25 carboxyterminal amino acids
by 17 amino acids encoded by the Stalker sequences and to a decrease of the
e(y)1 transcription level. The latter is the main cause of dramatic underd
evelopment of the ovaries and sterility of females bearing the e(y)1 mutati
on. This follows from the restoration of female fertility upon transformati
on of e(y)1(u1) flies with a construction synthesizing the mutant protein.
The e(y)1(P1) mutation induced by P element insertion into the transcribed
nontranslated region of the gene has almost no influence on the phenotype o
f flies. However, in combination with the ph(P1) mutation, which leads to a
strong P element-mediated suppression of e(y)1 transcription, this mutatio
n is lethal. Genetic studies of the e(y)1(u1) mutation revealed a sensitivi
ty of the yellow and white expression to the TAF(II)40/e(y)1 level. The su(
Hw)-binding region, Drosophila insulator, stabilizes the expression of the
white gene and makes it independent of the e(y)1(u1) mutation.