Frameshift mutation: 9 base pairs from positions 14 to 22 of the coding sequence have been deleted and substituted with GTCACGA. This is predicted to result in a truncated protein of 29 amino acid residues.
GTCACGA
The deletion of 9 base pairs and insertion of 7 (GTCACGA) leads to a frameshift and early translation terminaion.
STUB1I mutant adults exhibit reduced climbing ability along with age-progressive mitochondrial defects (decreased thoracic mtDNA content and disorganization of the cristae).
STUB1I/STUB1I is a non-enhancer of abnormal locomotor behavior | adult stage phenotype of parkΔ21/park1
STUB1I/STUB1I is a non-suppressor of abnormal locomotor behavior | adult stage phenotype of Pink1B9
The reduced climbing ability of park1/parkΔ21 mutants is not exacerbated by combination with STUB1I in homozygous state, but the lifespan of the double mutants is significantly decreased compared to park1/parkΔ21 single mutants. Similarly, the climbing deficit observed in Pink1B9 mutants is also not exacerbated by combination with STUB1I in homozygous state; lifespan of the double mutants is not significantly different from the Pink1B9 single mutants.
STUB1I is rescued by STUB1UAS.cCa/Scer\GAL4Mhc.PU
The reduced climbing ability of STUB1I mutant adults is rescued by Scer\GAL4Mhc.PU-driven expression of STUB1Scer\UAS.cCa.