Imprecise excision of the P{w+} element, resulting in a deletion of approximately 0.8kb that removes the open reading frame.
abnormal memory (with amn1)
Three-hour memory impairment after cold-induced anesthesia is not affected in amnX8 mutants. In contrast, reducing 5HT levels by pCPA feeding reduces 3 hour memory in amnX8 mutants.
Twenty-four hour memory in amnX8 mutants is impaired after 10 sessions of spaced training but not after massed training.
amnX8 mutant larvae show a significant delay in response to noxious heat compared to control flies. These flies also exhibit a delay in their jump response to noxious heat of 9 seconds.
amn28A/amnX8 females, both larvae and adults, display a prolonged latency in their responses to a noxious heat stimulus.
amnX8 mutants make choies according to their recent experience and completely ignore the past experience in a 60-60V 1hr delay choice, similar to wild-type. No significant difference is observed between the 1hr Anesthesia-resistant memory (ARM) of a single conditioning event and that followed by a second conditioning event in amnX8 mutants.
The choice PI in the 60-30 V 1hr delay protocol is not significantly different from the 30 V immediate memory PI in amnX8 mutants, compared to wild-type where it is significantly lower.
amnX8 flies have a defective olfactory memory. These flies fail to produce the increased calcium influx seen in the dorsal paired medial neurons of wild-type flies at 30 minutes after a conditioning of 3s exposure to odour, followed by a 60s odour stimulus applied simultaneously with 12 electric-shock pulses. Additionally, amnX8 flies exhibit poor 3 hour memory following odorant training, irrespective of the duration of temperature shifts applied after training. amnX8 flies show no difference to wild-type flies in their performance after 1 to 15 short training trials, consisting of 10s of CS odour, a single electric shock 9s late, 30s fresh air and a further 10s of CS odor. However, amnX8 flies' performance is lower than wild type when tested 2 hours after 10 training trials.
Muscles of third instar amnX8 mutant larvae show a reduction in the L-type Ca2+ current compared to control larvae.
amnX8 flies exhibit both short-term (3 min) and long term (3 hr) memory loss.
While OCT learning is indistinguishable from wild-type, amnX8 flies exhibit greatly reduced BA learning.
amnX8 mutant flies exhibit a significant MCH immediate memory defect.
amnX8 flies without olfactory organs display BA avoidance that is indistinguishable from wild-type flies lacking olfactory organs.
amnX8;Scer\GAL4c316/amnScer\UAS.cWa and amnX8;Scer\GAL4Mz717/amnScer\UAS.cWa flies learn to avoid benzaldehyde significantly better than amnX8 flies, although their performance is still significantly worse than that of wild-type flies. In contrast, OCT immediate memory of amnX8 flies is indistinguishable from wild-type flies and amnX8;Scer\GAL4c316/amnScer\UAS.cWa and amnX8;Scer\GAL4Mz717/amnScer\UAS.cWa flies.
Mutant animals, unlike wild-type, do not show significant age-related memory impairment, 1 hour memory in aged flies was not significantly different from young mutant flies.
Mutants exhibit increased perineurial glial thickness.
Shows defects in memory retention both immediately (initial learning) or 180 minutes (3 hour memory) after training.
Hemizygous males and homozygous females show increased sensitivity to ethanol in an inebriometer assay.
amnX8/amn28A is rescued by amnUAS.cWa/Scer\GAL4da.G32
amnX8/amn1 is rescued by amnUAS.cWa/Scer\GAL4c316
amnX8 is rescued by amnUAS.cWa/Scer\GAL4c316
amnX8 is rescued by Scer\GAL4c316/amnUAS.cDa
amnX8 is rescued by amnUAS.cWa/Scer\GAL4c316
amnX8 is not rescued by amnUAS.cWa/Scer\GAL4c309
amnX8 is not rescued by Scer\GAL4c747/amnUAS.cWa
The presence of amnScer\UAS.cWa under the control of Scer\GAL4da.G32 significantly rescues the delayed larval and adult response to noxious heat in amn28A/amnX8 females.
The ethanol sensitive phenotype is rescued by amnhs.PM expressed using heat shock. Three heat shocks at 24 hour intervals in adult flies is sufficient to fully rescue the ethanol-sensitive phenotype.