A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\CASKX-307

General Information
SymbolDmel\CASKX-307SpeciesD. melanogaster
NameFlyBase IDFBal0048070
Feature typealleleAssociated geneDmel\CASK
Allele class
MutagenX ray
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Description
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FB2013_03
FB2013_02
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hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
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Location
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Associated Sequence Data
DDBJ /
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GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
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Progenitor genotype
Nature of the lesion
Statement
Reference
Imprecise excision of the P-element causing a 90kb deletion including Caki coding sequences.
Caused by aberration
Cytology
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Mature CASK[X-307]/CASK[X-313] males show a extremely low overall level of immature-male courtship than the control. Courtship initiation latency of this mutant is also significantly longer than the control, with many males never initiating courtship during a 10 minute observation. Mature CASK[X-307]/CASK[X-313] males fail to habituate to immature male pheromones. CASK[P18]/CASK[X-307] flies exhibit significantly less movement than control flies. CASK[X-307]/CASK[X-313] flies exhibit significantly less movement than control flies. CASK[X-307]/CASK[X-313] flies have normal circadian locomotor rhythms and wild type free running periods.
CASK[X-307]/CASK[X-313] mutant flies exhibit an impairment in their flight ability compared to wild-type flies. Indirect flight muscle action potentials display significantly longer short- and long-latencies compared to wild-type controls. In some indirect flight muscles (approximately 5%) displaying a normal resting membrane potential, the stimulation of the giant fiber pathway fails to evoke a clear repsonse, which intead appears as a small depolarization. This lack of response remains unchanged with time as well as with increasing stimulus voltage or duration, suggesting that synaptic transmission is impaired in these fibers. The ability of the giant fiber pathway to follow continuous stimulation is also impaired. In contrast to wild-type flies, short-latency responses show a significant response decrement even at low stimulation frequencies in CASK[X-307]/CASK[X-313] mutant flies. Long-latency responses show habituation, as in wild-type. At stimulation frequencies between 1 and 3 Hz the onset of habituation occurs significantly earlier in CASK[X-307]/CASK[X-313] mutant flies than in wild-type. The percentage of CASK[X-307]/CASK[X-313] mutant flies that show habituation is lower than in wild-type controls. These flies are also less responsive to dishabituation. The resting membrane potential of indirect flight muscle fibers from CASK[X-307]/CASK[X-313] mutant flies is not significantly different from wild-type. Average miniature end-plate potentials (MEPPs) frequency in CASK[X-307]/CASK[X-313] mutant flies is significantly higher than in wild-type. Furthermore, average MEPPs amplitude is greater in CASK[X-307]/CASK[X-313] mutants. Latency values are much shorter in CASK[X-307]/CASK[X-313] mutants than in wild-type. In a walking optomotor assay, the frequency of correct turns is significantly lower in CASK[X-307]/CASK[X-313] mutants compared to wild-type flies. In a light intensity assay, the response of CASK[X-307]/CASK[X-313] mutants to decreasing light intensity mirrors that of wild-type flies. However, the response of CASK[X-307]/CASK[X-313] mutants at lower light intensities (below intermediate levels) suggest an impairment of visual function at low light intensity. CASK[X-307]/CASK[X-313] mutants exhibit a higher sustained ERG respones than in wild-type individuals. Although the ON transient amplitude is similar in both wild-type and CASK[X-307]/CASK[X-313] flies, OFF transients are significantly higher in CASK[X-307]/CASK[X-313] mutants than in wild-type individuals. These differences remain even when a high-intensity light stimulus is used instead of a low-intensity stimulus. Adaptation of the sustained response, induced by continuous 1Hz stimulation, is qualitatively similar in both CASK[X-307]/CASK[X-313] mutants and wild-type flies, whereas the amplitudes of the ERG sustained responses are significantly higher in CASK[X-307]/CASK[X-313] flies during the whole stimulation period.
CakiX-307/CakiX-313 double mutants fail to suppress courtship with mated females as normal and are defective for courtship habituation. Associative memory, is normal in mutants.
Walking speed and path length of CakiX-307/CakiX-313 transheterozygotes is considerably reduced, as studied in Buridan's paradigm. Vision seems not to be dramatically altered.
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Comments
Expression of CASK[Scer\UAS.cZa] pan-neuronally under the control of Scer\GAL4[elav-C155] fully rescues the neuromuscular junction miniature end-plate potential as well as the giant fiber habituation response defects found in CASK[X-307]/CASK[X-313] mutant females but does not rescue any of these defects in male progeny.
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Bloomington
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Discoverer
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CakiX-307/CakiX-313 transheterozygote is referred to as 'caki1', a deletion of genomic DNA encoding approximately 100 amino acids of the C-terminal part of Caki.
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hide Synonyms & Secondary IDs ( 7 )
Reported As
Symbol Synonym
CakiX-307
 
CASKX-307
 
Name Synonym
Secondary FlyBase IDs
hide References ( 6 )
Research paper
Slawson et al., 2011, Genetics 187(1): 171--184
Central Regulation of Locomotor Behavior of Drosophila melanogaster Depends on a CASK Isoform Containing CaMK-Like and L27 Domains. [FBrf0212754]
Bachmann et al., 2010, J. Neurosci. 30(17): 5811--5824
A perisynaptic ménage à trois between Dlg, DLin-7, and Metro controls proper organization of Drosophila synaptic junctions. [FBrf0210640]
Mueller et al., 2005, Genetics 171(3): 1137--1152
Genetic modifier screens on hairless gain-of function phenotypes reveal genes involved in cell differentiation, cell growth and apoptosis in Drosophila melanogaster. [FBrf0190751]
Zordan et al., 2005, J. Neurophysiol. 94(2): 1074--1083
Drosophila CAKI/CMG protein, a homolog of human CASK, is essential for regulation of neurotransmitter vesicle release. [FBrf0187895]
Lu et al., 2003, Neuron 40(6): 1185--1197
Regulation of the Ca2+/CaM-responsive pool of CaMKII by scaffold-dependent autophosphorylation. [FBrf0167958]
Martin and Ollo, 1996, EMBO J. 15(8): 1865--1876
A new Drosophila Ca2+/calmodulin-dependent protein kinase (Caki) is localized in the central nervous system and implicated in walking speed. [FBrf0087589]