Splice site mutation (G to A) within the kinase domain. This is predicted to cause intron retention and mis-translation of the intronic fragment after amino acid residue 1277, resulting in a truncation of the kinase domain.
G9254650A
G?A
Reported as a G to A mutation in a splice site after amino acid residue 1277. The position of mutation on reference sequence was inferred by a FlyBase curator. The isoforms relative to which the mutation was mapped was not specified.
Females with Pkn1T/Pkn1T germline clones show no significant difference in total number of eggs or egg laying distribution compared to controls, but egg length is significantly reduced (though dorsal appendages are usually normally positioned).
During nurse cell dumping, egg chambers mutant for Pkn1T/Pkn1T show increased nurse cell-to-oocyte membrane collapse, leading to abnormal presence of ring canals, border cells and/or nurse cell nuclei in the oocyte cytoplasm.
Nurse cell adherens junctions and somatic follicular epithelial cells look normal, and no significant morphological defects are detected in ring canals or nurse cell cytoplasmic actin cables in Pkn1T/Pkn1T mutant germline clone egg chambers during early oogenesis. In mid-oogenesis there is an increase in the frequency of nurse cell-to-nurse cell membrane collapse (leading to multinucleated nurse cells after stage 6/7) in Pkn1T/Pkn1T mutant germline clone egg chambers.
Females with Pkn1T/Pkn1T germline clones show high abnormal accumulation of F-actin and myosin in nurse cells of stage 10 egg chambers, with an abnormally thick activated actin-myosin cytoskeleton with significant discontinuities that frequently radiates outwardly perpendicular to the anterior-posterior axis of the egg chamber.
Average nurse cell slow dumping rates in egg chambers from freshly dissected ovaries of Pkn1T/Pkn1T germline clones are not significantly different to controls, whereas fast dumping rates are significantly slower than controls.
Pkn1T has egg | germline clone phenotype, enhanceable by sqhRLC.GFP(S65T)/sqhRLC.GFP(S65T)
Pkn1T has egg | germline clone phenotype, enhanceable by sqhE20.E21/sqh[+]
Pkn1T has egg | germline clone phenotype, enhanceable by flw[+]/flwG0172
Pkn1T has egg | germline clone phenotype, non-enhanceable by Scer\GAL4nanos.PU/RokUAS.cUa.Tag:HA
Pkn1T has egg | germline clone phenotype, non-enhanceable by flw[+]/flw1
Pkn1T has egg | germline clone phenotype, suppressible | partially by cpbM143/cpb[+]
Pkn1T has nurse cell | germline clone phenotype, suppressible | partially by cpbM143/cpb[+]
Pkn1T/Pkn1T is an enhancer of egg phenotype of sqhE20.E21
Pkn1T/Pkn1T is a non-enhancer | germline clone of egg phenotype of RokUAS.cUa.Tag:HA, Scer\GAL4nanos.PU
Presence of cpbM143/+ partially suppresses the shorter egg length and nurse cell F-actin accumulation seen in Pkn1T/Pkn1T germline clone egg chambers.
sqhRLC.T:Avic\GFP-S65T/sqhRLC.T:Avic\GFP-S65T or sqhE20.E21/+ or flwG0172/+ enhances the shorter egg length phenotype seen in Pkn1T/Pkn1T germline clones.
Overexpression of RokScer\UAS.T:Ivir\HA1 driven by Scer\GAL4nos.PU, or flw1/+, does not enhance the shorter egg length phenotype seen in Pkn1T/Pkn1T germline clones.
The shorter egg length phenotype seen in females with overexpression of RokScer\UAS.T:Ivir\HA1 driven by Scer\GAL4nos.PU is not enhanced in Pkn1T/Pkn1T germline clones.