Mutation results in a protein that lacks the carboxy-terminal 25 amino acids.
Amino acid replacement: Q491term.
C9916820T
Q493term | Mef2-PA; Q486term | Mef2-PB; Q492term | Mef2-PC; Q517term | Mef2-PD; Q478term | Mef2-PF; Q488term | Mef2-PG; Q486term | Mef2-PH; Q453term | Mef2-PI; Q511term | Mef2-PJ; Q459term | Mef2-PK; Q499term | Mef2-PL
Q491term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change
Mef265/Mef2113 embryos exhibit a reduction in the number of dorsal longitudinal indirect flight muscles to three pairs due to defects in the template splitting process.
Mef225-42/Mef265 trans-heterozygotes exhibit major defects in their indirect flight muscles, based on reduced numbers and abnormal patterning of the dorsal longitudinal indirect flight muscles.
Mef226-6/Mef265 trans-heterozygotes exhibit major defects in their indirect flight muscles, based on reduced numbers and abnormal patterning of the dorsal longitudinal indirect flight muscles.
Mef225-34/Mef265 trans-heterozygotes exhibit a wild-type pattern and number of dorsal longitudinal indirect flight muscles.
Mef265/Mef2424 adults survive at 20-30% rate of sibling classes. Eggs laid by Mef265/+ show 92.3% wild type dorsal appendages, 6.2% reduced dorsal appendages and 1.5% broad dorsal appendages and normal egg length. Eggs laid by Mef265/Mef2424 females show 36.9% wild type dorsal appendages, 24.2% reduced dorsal appendages, 19.9% broad dorsal appendages and short egg length, 8.5% broad dorsal appendages and normal egg length, 6.9% abnormal dorsal appendages with short egg length and 3-6% cup-like eggs with no dorsal appendages and cup-like shape.
The three persistant larval oblique muscles per hemithorax of Mef265/Mef2113 animals escape from histolysis as in wild-type animals. Splitting of these muscles generally does not occur in Mef265/Mef2113 animals in contrast to wild-type, so that the number of dorsal longitudinal indirect flight muscles is reduced.