Df(2L)Msp-300-3 removes the 3' section of the Msp-300 locus, including the KASH domain, between PBac{WH}f05524 and P{XP}d01768.
egg (with Msp300ΔKASH)
Body wall muscles in Msp3003prime homozygous third instar larvae frequently show nuclei clustering together or in contact with each other, instead of the typically even spaced in controls.
The striated muscle in Msp-3003prime mutant third instar larvae exhibits aggregation of the myonuclei and aberrant nuclear shape, as well as variable nuclear size. In contrast to wild to wild type, where the nuclei are tightly associated with the myofibril compartment, Msp-3003prime mutant myonuclei are dissociated from the core acto-myosin compartment and float above it. The sarcomeric organisation of the muscles is retained.
Muscles from third instar larvae homozygous mutant for Msp-3003prime show clustering of the mitochondria and endoplasmic reticulum.
Homozygous klarΔ1-18 mutant larvae exhibit a 70% reduction in their motility compared to wild type.
Adult flies homozygous mutant for Msp-3003prime are unable to fly.
Msp-3003prime homozygotes are semi-lethal (approximately 20% of expected homozygotes survive). They do not display any obvious phenotype and move normally. Over time, the movements become slower and the larvae die before entering the second instar. There is no detectable difference in the arrangement or the movement of the body wall muscles of wild-type and mutant individuals when observing the larvae in polarised light.
Msp-3003prime homozygous flies, in which the KASH domain coding part of the Msp-300 locus is deleted, exhibit normal eyes.
Msp-3003prime homozygous females lay normal eggs.
Msp-3003prime germline clones lay normal eggs, with no observable defects in nuclear position or nuclear architecture in the egg chambers.
Female Msp-3003prime;klarmarb-BX12 double mutants lay normal eggs and exhibit wild-type egg chambers.
A Dp(2;1)B19 background rescues the semi-lethality of Msp-3003prime mutants.