Homozygous and salsf07849/Df(3R)M-Kx1 embryos fail to hatch from the egg case (100% penetrance) and show similar muscle defects.
Primary muscle cultures derived from myoblasts dissociated from homozygous mutant embryos have a reduced sarcomere length and myofibril width, but normal myofibril length compared to control cultures.
Stage 16 homozygous embryos have normal overall muscle morphology, and the number of nuclei in mutant muscles is comparable to that in wild type.
Muscles in late stage 17 mutant embryos have myofibrils with numerous short sarcomeres (they show an approximately 27% reduction in length compared to wild type). In addition, the mutant myofibrils are thin and split and are distributed along the lateral side of muscles. The thin filaments are significantly shorter in length than normal. The nuclei of the mutant muscles are localised more towards the muscle ends (wild-type muscles have even distributed nuclei).
The muscles of mutant larvae at 28-30 hours after egg laying contain many more sarcomeres than those of control larvae, but they are much shorter in length longitudinally compared to controls. Some of the mutant muscles show a complete disruption of myofibril morphology.
Peristaltic movement is detectable in later stage 17 mutant embryos, however, the mutant embryos have less frequent backward peristalsis than controls, and the vigour of their contraction is much reduced. At 28-30 hours after egg laying (the expected hatch time), the mutants show weak movement. They eventually die in the egg case within a day. If mutant animals are manually removed from the egg case, they are flaccid and immobile.
salsf07849 is an enhancer of lethal | embryonic stage phenotype of Scer\GAL4Mef2.PR, tmodUAS.cBa
salsf07849 is an enhancer of striated muscle thin filament phenotype of Scer\GAL4Mef2.PR, tmodUAS.cBa
salsf07849/sals[+] is a non-enhancer of indirect flight muscle cell phenotype of DAAMEx1
salsf07849/sals[+] is a non-suppressor of indirect flight muscle cell phenotype of DAAMEx1
The mild indirect muscle phenotype seen in DAAMEx1 mutants is not altered by salsf07849/+.
salsf07849 enhances the lethality cause by expression of tmodScer\UAS.cBa under the control of Scer\GAL4Mef2.PR, such that a greater fraction of the animals die as embryos.
The reduction in thin filament length seen in primary cultured muscle cells isolated from embryos expressing tmodScer\UAS.cBa under the control of Scer\GAL4Mef2.PR is increased if the animals are also carrying salsf07849.
salsf07849 is rescued by salsΔProR.UAS.Tag:FLAG/Scer\GAL4Mef2.PU
salsf07849 is rescued by salsUAS.Tag:FLAG/Scer\GAL4Mef2.PU
salsf07849 is rescued by Scer\GAL4Mef2.PU/salsWH2.Cterm.UAS.Tag:FLAG
salsf07849 is rescued by salsUAS.cBa/Scer\GAL4Mef2.PR
salsf07849 is not rescued by Scer\GAL4Mef2.PU/salsΔProR.WH2.UAS.Tag:FLAG
salsf07849 is not rescued by Scer\GAL4Mef2.PU/salsΔWH2.UAS.Tag:FLAG
salsf07849 is not rescued by salsCterm.UAS.Tag:FLAG/Scer\GAL4Mef2.PU
salsf07849 is not rescued by salsNterm.UAS.Tag:FLAG/Scer\GAL4Mef2.PU
salsf07849 is not rescued by Scer\GAL4Mef2.PU/salsProR.WH2.Nterm.UAS.Tag:FLAG
salsf07849 is not rescued by salsProR.WH2.UAS.Tag:FLAG/Scer\GAL4Mef2.PU
Mobilisation of the insertion can fully revert the lethal phenotype.