Nucleotide substitution: C559T.
Amino acid replacement: Q187term.
C16954532T
C559T
Q187term | mute-PC
Q187term
Females containing homozygous germline clones do not lay eggs.
Homozygous stage 16 embryos show a severe loss of muscle mass compared to controls.
mute1281/Df(2R)Exel6065 embryos show no significant difference in somatic muscle mass or morphology at stage 14 compared to control embryos. However, by stage 15, some muscles appear thinner than normal in the mutant embryos and some muscles are no longer detectable. At stage 16, many muscles appear significantly thinner than normal in the mutant embryos and some muscles are no longer detectable. This phenotype is not biased to any specific somatic muscle type and some of the muscles appear to detached at least at one end. By stage 17, the muscles have degenerated so that they have lost the characteristic wild-type morphology and are spherical in shape or are extremely thin.
mute1281/Df(2R)Exel6065 has larval somatic muscle cell phenotype, non-suppressible by Df(3L)H99
Slbp15, mute1281/mute[+] has larval somatic muscle cell phenotype
The thin muscles characteristic of late stage mute1281/Df(2R)Exel6065 embryos are still seen if they are also homozygous for Df(3L)H99.
More than half of mute1281/+ ; Slbp15/Slbp15 stage 16 embryos have somatic muscles that appear significantly thinner than normal. Some muscles are detached while others appear to be missing.
mute1281/Df(2R)Exel6065 is rescued by Scer\GAL4how-24B/muteL.UAS
mute1281/Df(2R)Exel6065 is rescued by Scer\GAL4how-24B/muteΔC.L.UAS
mute1281/Df(2R)Exel6065 is partially rescued by Scer\GAL4how-24B/muteS.UAS
mute1281/Df(2R)Exel6065 is not rescued by Scer\GAL4how-24B/muteΔC-Atro.L.UAS
The muscle wasting phenotype of mute1281/Df(2R)Exel6065 embryos is completely rescued by expression of muteL.Scer\UAS or muteΔC.L.Scer\UAS under the control of Scer\GAL4how-24B.
The muscle wasting phenotype of mute1281/Df(2R)Exel6065 embryos is not rescued by expression of muteΔC-Atro.L.Scer\UAS under the control of Scer\GAL4how-24B.
The muscle wasting phenotype of mute1281/Df(2R)Exel6065 embryos is partially rescued by expression of muteS.Scer\UAS under the control of Scer\GAL4how-24B.