STUDIES ON DROSOPHILA EMBRYONIC CELLS IN VITRO II. TISSUE- AND TIME-SPECIFICITY OF A LETHAL GENE, DEEP ORANGE

Embryonic cells which were homozygous or hemizygous for an X-linked (1-0.3) recessive lethal gene, deep orange (dor), were cultured in T-5 flasks. Muscle cells, epithelial cells, fibroblastic cells and nerve cells were maintained in a functionally active state for longer than the effective lethal phase of the embryos. Some defects in syncytium formation of muscle cells, formation of cellular spheres, and droplet formation on nerve fibers were observed. Addition of an extract of unfertilized wild-type eggs to the culture medium resulted in repair of these defective characters of dor embryonic cells. To examine the time specificity of the paternal dor+ gene, extracts of embryos obtained from matings of dor sn3 /dor sn3 females and dor+ sn3+ /Y males were tested for their ability to repair the defects of dor embryonic cells. The extract from embryos at the stage of blastoderm formation was not effective in repairing dor defects, but extracts from embryos at stages after gastrulation were effective for repair of various defects of dor embryonic cells. Various substances in the pteridine metabolic pathway were tested for their ability to repair defects of dor embryonic cells. The effective lethal phase of dor embryos and the pleiotropic effects of the dor gene are discussed.