B. Poeck et al., EXPRESSION OF THE DROSOPHILA-OPTOMOTOR-BLIND GENE TRANSCRIPT IN NEURONAL AND GLIAL-CELLS OF THE DEVELOPING NERVOUS-SYSTEM, Development, 117(3), 1993, pp. 1017-1029
Mutations in the complex gene locus optomotor-blind (omb) can lead to
defects in the development of both the optic lobes and external featur
es of the adult fly. We describe here the expression of omb in the dev
eloping and adult nervous system using in situ hybridization. During e
mbryogenesis, omb expression is first observed in the optic lobe anlag
en. It later expands to a larger part of the developing larval brain a
nd to the gnathal lobes. Cells in the ventral and peripheral nervous s
ystems begin to express omb after completion of germ band extension. L
ater in embryonic development, expression declines and only persists i
n the antenno-maxillary complex and in part of the brain hemispheres.
During the larval and pupal stages, omb expression in the brain is con
fined to the developing optic lobes and contiguous regions of the cent
ral brain. At these stages, only a few cells show expression in the ve
ntral ganglion. In the eye imaginal disc, transcript accumulation is m
ost conspicuous in a group of presumptive glia precursor cells posteri
or to the morphogenetic furrow and in the optic stalk. In the adult br
ain, expression is prominent in several regions of the optic lobe cort
ex and along the border between central brain and optic lobes. In the
mutation In(1)omb(H31), 40 kb of regulatory DNA, downstream from the t
ranscription unit, are removed from the omb gene. In(1)omb(H31) is cha
racterized by the lack of a set of giant interneurons from the lobula
plate of the adult optic lobes. We find that, already during embryogen
esis, there is a drastic difference between wild type and In(1)omb(H31
) in the level of the omb transcript in the optic lobe primordia. The
adult mutant phenotype may thus be caused by omb misexpression during
embryonic development.