FlyBase curator comment: this entry is used to capture phenotypic information when the particular allele (or allele combination) used by the author could not be determined but the context of the experiment suggests that the phenotype being described is some kind of loss of function.
Mutant embryos have alterations in embryonic morphology. No epidermal folds are found below the ventral nerve cord. Instead of stretching dorsally, the ectoderm appears to fold like an accordion in the anterior-posterior axis. As a consequence the gut is frequently pushed outside the embryo. By the end of embryogenesis the ventral folding of the epidermis pushes the ventral nerve cord further deep into the embryo. Beside the dorsal closure phenotypes, defects are also seen during head involution and in gut morphology. Mutant embryos also typically have fused commissure phenotypes where anterior and posterior commissures are not separated. Longitudinal connectives are also often reduced and frequent gaps may be seen in tracts. Glial cell organisation is severely affected in mutants. Mutants have a significant increase in the number of midline glial cells. About 6 cells are seen per neuromere.
Cuticle and head structures are undifferentiated in dibunspecified mutant embryos.
dibunspecified has midline glial cell | ectopic phenotype, enhanceable by Scer\GAL4sim.PS/BacA\p35UAS.cHa
In dibunspecified, BacA\p35Scer\UAS.cHa, Scer\GAL4sim.PS embryos, about 10 midline glial cells are seen per neuromere.
In dibunspecified, BacA\p35Scer\UAS.cHa, Scer\GAL4sim.PS embryos, about 10 midline glial cells are seen per neuromere.
dibunspecified is rescued by dib+tSE9
dibunspecified is rescued by dib+tHS
dibunspecified is rescued by dib+tSE20
dibunspecified is not rescued by dibtSE32
Eleven alleles have been isolated.