Part of the gene is deleted.
Deletion extends from the original site of insertion of P{lArB}MB2487, at approximately 25kb upstream of the 5' end of the Mef2 transcription unit, to 320bp upstream of the start of Mef2 transcription such that the proximal end of the P{lArB} is inserted into the Mef2 promoter.
The wavy morphology of the dorso-ventral muscle myofibrils of pupae expressing Mef2GD5039 under the control of Scer\GAL4Act88F.PB is worsened if the animals also carry Mef2P544.
Muscle founder cells never differentiate to form mononucleate muscles. Con, vg or Fas3-expressing founder cells show that target recognition takes place and motoneurons that establish contact are always attracted to the correct founder cells. Myoblast fusion and Mhc and βTub60D expression are severely affected, thus general features of differentiated muscle are deranged or missing. Normal neuromuscular junctions are wholly absent.
Mef2P544, twi1/twi[+] has mesothoracic tergotrochanter muscle cell phenotype, enhanceable by brnpr-3/br[+]
Mef2P544, brnpr-3/br[+] has mesothoracic tergotrochanter muscle cell phenotype, enhanceable by twi1/twi[+]
Mef2P544 has mesothoracic tergotrochanter muscle cell phenotype, enhanceable by brnpr-3/br[+]
Mef2P544 has mesothoracic tergotrochanter muscle cell phenotype, enhanceable by twi1/twi[+]
Mef2[+]/Mef2P544 is an enhancer of dorsal longitudinal indirect flight muscle cell phenotype of brnpr-3/br[+], twi1
Mef2[+], brnpr-3, Mef2P544, br[+] is an enhancer of mesothoracic tergotrochanter muscle cell phenotype of twi1
Mef2[+], twi1, Mef2P544, twi[+] is an enhancer of mesothoracic tergotrochanter muscle cell phenotype of brnpr-3
Mef2P544, brnpr-3/br[+], twi1/twi[+] has dorsal longitudinal indirect flight muscle cell phenotype
Mef2[+]/Mef2P544, brnpr-3, twi1/twi[+] has dorsal longitudinal indirect flight muscle cell phenotype
While both twi1/+, Mef2P544/+ and brnpr-3/+; Mef2P544/+ double mutants show a wild-type number of DLM fibers, brnpr-3/+; twi1/+, Mef2P544/+ triple mutants show a reduced numbers of these fibers (5.2 vs 6 in wild type).
brnpr-3/+; Mef2P544/+ double heterozygotes display higher levels of defects in TDT organization than either single heterozygote, including the presence of ectopic fibers in the lumen. twi1/+, Mef2P544/+ also show an increase in the number of TDT defects compared to single mutants. 82% of brnpr-3/+; twi1/+, Mef2P544/+ triple mutants show defects in TDT patterning (a higher level than any of the double mutant combinations), including additional small cells, internal fibers and the rerouting of some fibers to the periphery.