The lethal of scute (l'sc) genetic function, which plays an essential
role in the early development of the central nervous system of the Dro
sophila embryo, is localized within the achaete-scute complex (AS-C).
Several lines of evidence have suggested that the AS-C T3 transcriptio
n unit corresponds to the l'sc function. We demonstrate that short fra
gments of DNA, containing the T3 transcribed region and a few kilobase
s of flanking sequences, rescue, albeit partially, the lethality and n
eural phenotype of l'sc deletions. Still, the complex wild-type patter
n of expression of T3 is not reproduced by the transduced genes. This
depends on cis-control elements scattered within the entire AS-C DNA a
nd intermingled with regulatory elements specific for other AS-C trans
cription units. These elements are necessary for the initial activatio
n of T3 in the neuroectoderm, probably mediated by axis-patterning gen
es. The presence of a cluster of F-boxes, upstream of the T3 transcrib
ed region, suggests another level of control of T3 expression by basic
-helix-loop-helix proteins, among them its own gene product.