Amino acid replacement: Q668term.
C23325936T
Q668term | alpha-Cat-PA
Q668term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
α-Cat2049 mutant embryos show anterior cuticle defects and frequently display holes, some also develop a completely dorsal open phenotype or dorsal holes. The mutants display a reduction in the velocity of progression of the leading edge during dorsal closure compared to wild-type controls, this is not due to a decrease in the number of cell delamination events as this is actually increased in the mutants while the total number of amnioserosa cells at the onset of tissue contraction is comparable to controls. There are however significant aberrations in the oscillatory and contractile behavior of amnioserosa cells during the dorsal closure process: whereas the amplitude of cell oscillations is only mildly affected, the period is clearly increased as is the length of both contraction and expansion half-cycles, the rate of apical cell contraction is lower and the cells develop a corrugated appearance. The actomyosin dynamics in these cells is perturbed.
α-Cat2049 has embryonic/larval cuticle | embryonic stage phenotype, enhanceable by Df(1)Vinc2
α-Cat2049 has embryonic/larval cuticle | embryonic stage phenotype, non-enhanceable by sqhDD.UAS/Scer\GAL4c381
The severity of the embryonic cuticle defects characteristic for α-Cat2049 mutants is aggravated by combination with Df(1)Vinc2 but not by expression of sqhDD.Scer\UAS under the control of Scer\GAL4c381 in the mutant background.