Amino acid replacement: S224L.
C14259090T
S224L | MetRS-m-PA; S224L | MetRS-m-PB; S224L | MetRS-m-PC
S224L
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
abnormal neurophysiology | adult stage | somatic clone | conditional (with MetRS-mHV)
flightless (with MetRS-mHV)
lethal | pupal stage (with MetRS-mc00449)
short lived (with MetRS-mHV)
Aats-metFB mutants exhibit abundant lipid droplet accumulations in pigment and epithelial glia. In addition to the retina, lipid droplets also accumulate in the epithelial glia of the lamina.
Aats-metFB mutant visual system clones (generated with hidGMR.PG) exhibit lipid droplet accumulation in the glia.
The morphology of Aats-metFB mutant photoreceptors is mostly normal or only mildly affected at day 1. They begin to degenerate several days after eclosion, with elongated or diffuse rhabdomeres. One-day old Aats-metFB clones exhibit approximately 10 lipid droplets per ommatidium. Upon aging, these clones display a significant decrease in the number of lipid droplets.
1 day old flies containing large clones of homozygous tissue in the eye have an electroretinogram (ERG) with a significantly reduced amplitude compared to wild type. The ERG amplitude decreases as the flies age.
Aats-metHV/Aats-metFB adult escapers have normal ERGs at 1 day old, while the ERG is severely abnormal in 3 week old flies. The rhabdomeres and overall structure of the photoreceptors appears normal, with the correct number of photoreceptors per ommatidium in 1 day old flies. The total mitochondrial area in the mutant photoreceptors is greater than normal in 1 day and 1 week old flies. Lipid droplets are present in the pigment cells in mutant flies, a phenotype not seen in wild type. The photoreceptors and glial cells progressively degenerate, such that by 3 weeks of age, most photoreceptors are severely affected and many organelles are barely recognisable.
Homozygous and Aats-metHV/Aats-metFB flies have shorter lifespans than normal and are unable to fly.
The myofibrils of the indirect flight muscles appear intact in 1 day old Aats-metHV/Aats-metFB flies, but the mitochondria are clearly abnormal, being larger than normal. The myofibrils show defects in 1 week old flies and the mitochondria are very large.
Aats-metFB/Df(3R)Exel7321 pupae are shorter than normal.
Homozygous clones in the wing disc are smaller than their wild-type twin spots.
MetRS-mFB/Df(3R)Exel7321 has lethal phenotype, suppressible by Scer\GAL4Act5C.PU/Hsap\MARS2UAS.cBa
A bsk1 heterozygous background is sufficient to ameliorate the lipid droplet accumulation displayed in Aats-metFB mutants.
A SREBP189 heterozygous background is sufficient to ameliorate the lipid droplet accumulation displayed in Aats-metFB mutants.
Expression of Lip4Scer\UAS.cLa in Aats-metFB mutant clones partially restores the shape, density and number of identifiable rhabdomeres, indicating that reducing lipid droplet accumulation partially alleviates neurodegeneration.
Expression of bmmScer\UAS.cGa in Aats-metFB mutant clones partially restores the shape, density and number of identifiable rhabdomeres, indicating that reducing lipid droplet accumulation partially alleviates neurodegeneration.
Expression of Hsap\SOD1Scer\UAS.cPa under the control of Scer\GAL4da.G32 in Aats-metFB mutant larvae reduces the overall level of reactive oxygen species and considerably suppresses the lipid droplet accumulation seen in these flies.
Expression of Hsap\MARS2Scer\UAS.cBa under the control of Scer\GAL4Act5C.PU rescues the lethality of Aats-metFB/Df(3R)Exel7321 flies.
MetRS-mFB/Df(3R)Exel7321 is rescued by Scer\GAL4Act5C.PU/MetRS-mUAS.cBa