127bp deletion.
Deletion in the third coding exon of bark resulting in a frame-shift and a premature stop codon six codons thereafter. This should truncate the protein to 587 aa after the CUB-like domain in region I of the extracellular part.
A 127 bp deletion that results in a frameshift and a premature stop codon 6 amino acids downstream.
barkL200 embryonic epidermis exhibit disappearance of the low mobility of GFP::M6 at tricellular junctions.
barkL200 clones of dividing epithelial cells have membrane deformations, disruptions in the integrity of septate junctions and an accelerated basal displacement of the midbody. The assembly and stability of septate junctions are unaffected.
barkL200 clones of epithelial cells have normal finger-like protrusions associated with the midbody of neighboring dividing cells.
Mutant embryos show excessively elongated tracheal tubes. Stage 17 barkL200 embryos also show 'cavities' in the tracheal epithelium, seen as round areas 0.5-6 mm in diameter, that form between neighbouring cells. Similar structures are evident in the epidermis.
The formation and correct geometry of tricellular junctions, but not bicellular septate junctions, is defective in barkL200 embryos.
barkL200 has decreased cell size | somatic clone | P-stage phenotype, suppressible by crb11A22
barkL200 has decreased cell size | somatic clone | P-stage phenotype, suppressible by mysJF02819/Scer\GAL4Tub.PU
barkL200 has cell-cell junction | somatic clone | P-stage phenotype, suppressible by mysJF02819/Scer\GAL4Tub.PU
barkL200 has epithelial cell | somatic clone | P-stage phenotype, suppressible by mysJF02819/Scer\GAL4Tub.PU
barkL200 has epithelial cell | somatic clone | P-stage phenotype, suppressible | partially by crb11A22
barkL200 has cell-cell junction | somatic clone | P-stage phenotype, non-suppressible by crb11A22
barkL200 is rescued by barkUAS.cBa/Scer\GAL4btl.PU
barkL200 is rescued by Scer\GAL4btl.PU/barkΔPDZB.UAS
Scer\GAL4btl.PU-mediated expression of barkScer\UAS.cBa or barkΔPDZB.Scer\UAS rescues the tracheal defects of barkL200 embryos.