Small deletion.
embryonic brain & commissure
The protocerebral brain anlage fails to develop in mutants and the preoral brain commissure is not formed.
The protocerebral brain anlage fails to develop in homozygous embryos, and the preoral brain commissure is missing or severely reduced. Ubiquitous overexpression of ochs.PR in homozygous embryos at stage 7-8 results in restoration of anterior brain morphology in over half the heat shocked embryos. Rescue of the embryonic brain phenotype by overexpression of ochs.PR is not possible after stage 8. Ubiquitous overexpression of Hsap\OTX2hs.PN in homozygous embryos at stage 7-8 results in restoration of anterior brain morphology in 45% of heat shocked embryos. Ubiquitous overexpression of Hsap\OTX1hs.PN in homozygous embryos at stage 7-8 results in restoration of anterior brain morphology in over one-fifth of heat shocked embryos. Rescue of the embryonic brain phenotype by overexpression of ochs.PR, Hsap\OTX1hs.PN or Hsap\OTX2hs.PN is not possible after stage 8. Homozygous embryos have deranged connectives and fused commissural axon tracts in the ventral nerve cord. This phenotype can be rescued by ubiquitous overexpression of ochs.PR at stage 10-11. The phenotype can be rescued in 100% of cases by ubiquitous overexpression of Hsap\OTX2hs.PN at stage 10-11. The phenotype can be rescued in over 90% of cases by ubiquitous overexpression of Hsap\OTX1hs.PN at stage 10-11. Rescue is not seen if ochs.PR, Hsap\OTX1hs.PN or Hsap\OTX2hs.PN is expressed before stage 10 or after stage 11.
Neuromere b1 is absent or reduced in all embryos.
Median ocellus is displaced anteriorly and is smaller. The pattern of interocellar and ocellar bristles is disturbed. The distance between the two lateral ocelli and between the two postvertical bristles is increased. Phenotypic series from the strongest to weakest oc allele: ocdb/ocdb > oc1/oc+ > ocγa1/oc+ > oc2/oc+ > oc1/oc1 > ocγa1/ocγa1 > oc2/oc1 > oc2/ocγa1.
The dorsal arms of the head skeleton are absent or fragmented in mutant embryos. The antennal segment is missing.
Defects in head development and segmental patterning. Abnormal neuropil. Aberrant commissure formation in each segment. The disappearance of neurons labelled by a P{A92}45C demonstrate that cell death is restricted to identified neurons associated with the midline of the CNS.
oc2 has embryonic brain & commissure phenotype, suppressible by Hror\Otxhs.PA
oc2 has embryonic brain & commissure phenotype, suppressible by Hsap\OTX2hs.PN
oc2 has embryonic protocerebrum phenotype, suppressible by Hror\Otxhs.PA
oc2 has embryonic protocerebrum phenotype, suppressible by Hsap\OTX2hs.PN
The embryonic brain defects of oc2 animals are partially rescued by Hsap\OTX2hs.PN or Hror\Otxhs.PA.
non-complementing allele
Lefevre.
Less than 50% of wild type number of ventral epidermal cells expressing P{lacZ}BP28 are evident in mutant embryos.