Amino acid replacement: M184S.
Amino acid replacement: S181R.
ATG9692491AGY
M184S | Uba1-PA; M1S | Uba1-PC
M184S
The reported Met to Ser amino acid change (ATG to AGY) requires nucleotide changes at two positions of the codon. The site of the nucleotide substitution in the mutant was inferred by FlyBase based on the reported amino acid change. One of 2 missense mutations associated with this allele.
A9692500C
S181R | Uba1-PA
S181R
Amino acid replacement reported as reported as Ser to Arg, which could result from a nucleotide substitution in the first or second base of the codon. The mutation was annotated at the first base of the codon. One of 2 missense mutations associated with this allele.
Uba1B1/+ mutant flies display a significant decrease in lifespan as compared to wild type.
Very few Uba1B1/Uba1B1 mutants reach adulthood, and those that do are short lived, infertile, climbing defective, and display visible abnormalities including extra sternopleural bristles, loss of one or more dorsocentral bristles, ectopic wing veins, unusually thick wing veins, and abnormal wing posture.
Very few Uba1B1/Uba1B2 mutants reach adulthood, and those that do are infertile, climbing defective, and display visible abnormalities including unusually thick wing veins.
Uba1B1 homozygous and Uba1B1/Uba1B2 trans-heterozygous eye discs exhibit a significant increase in proliferation (as observed through phosphorylated His3 signal). Ectopic proliferation posterior to the morphogenetic furrow is significant enough that the region of frequent anti-pHis3 staining extends two to three times as far into the region posterior to the morphogenetic furrow.
Uba1B1 homozygous adults reveal occasional overgrowths, such as outgrowths on the leg, proboscis or humeral regions consistent with ectopic divisions.
Only a small percentage of Uba1B1 homozygotes reach adulthood.
Homozygous clones in the eye have a growth advantage compared to surrounding wild-type tissue.
Uba1B1 has short lived phenotype, suppressible | partially by Ras85De1B/Ras85D[+]
Ras85De1B/Ras85D[+], Uba1B1/Uba1B2 has viable phenotype, suppressible by egrUAS.cMa/Scer\GAL4GMR.PF
Uba1B1/Uba1B2 has eye disc posterior to the morphogenetic furrow phenotype, suppressible by Ras85De1B/Ras85D[+]
The cell-autonomous overgrowth phenotype found in Uba1B1 homozygous and Uba1B1/Uba1B2 trans-heterozygous eye discs is suppressed in a Ras85De1B heterozygous background.
A Ras85De1B/+ background dramatically suppresses the lethality found in Uba1B1/Uba1B2 homozygotes.
Uba1B1/Uba1B2 eyes in a Ras85De1B heterozygous background show decreased suppression of egrScer\UAS.cMa (under the control of Scer\GAL4GMR.PF) induced cell death.
Overall cell proliferation in Uba1B1/Uba1B2 eye discs is reduced in a Ras85De1B/+ background. Ectopic proliferation posterior to the morphogenetic furrow decreases and is restricted to a thin stripe.
A Egfrk05115/+, drkk02401/+, or Sose4G/+ background does not suppress the ectopic cell divisions found in Uba1B1/Uba1B2 trans-heterozygous eye discs.