Construct: Amino acid replacement: G245D.
Mutation causes myofibrillar disruption even in the presence of two wild type alleles and induces the synthesis of heat shock proteins. In Act88FGD245 heterozygotes the mutant actin was initially incorporated into myofibrils and later induced their degeneration from center to periphery. Act88FGD245 homozygotes have severe indirect flight muscle deformation and abdominal swelling.