Allele Dmel\stnA12
| General Information | |||
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| Symbol | Dmel\stnA12 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0016212 | |
| Feature type | allele | Associated gene | Dmel\stnA |
| Also Known As | stn13-120 | ||
| Allele class | hypomorphic allele - genetic evidence | ||
| Mutagen | spontaneous | ||
Recent Updates
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Nature of the Allele
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| Allele class | |||
| Mutagen | |||
| Mutations Mapped to the Genome | |||
Type Location Additional Notes References | |||
| Associated Sequence Data | |||
| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
| UniProtKB/Swiss-Prot | |||
| UniProtKB/TrEMBL | |||
| Progenitor genotype | |||
| Nature of the lesion | Statement Reference Insertion into ORF1. Doc element insertion. | ||
| Caused by insertion | |||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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Detailed Description
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Statement Reference Mutants die as mature embryos after a failure to hatch, due to lack of coordination. Mutant embryos show normal segmental patterning of the epidermis, muscles and nervous system. Mutant nmjs appear morphologically wild type though the nerve terminals are slightly smaller than normal. In electrophysiological recordings at the embryonic nmj nerve stimulation produces muscle contraction demonstrating that presynaptic depolarization evokes transmitter release and that muscle excitation-secretion response is intact. However evoked EJC peak amplitudes are significantly reduced and the release of neurotransmitter at mutant synapses is markedly asynchronous due to delayed presynaptic vesicle fusion. Mutants have an impaired ability to synchronously trigger calcium-mediated vesicle fusion. The overall level of neurotransmitter release is reduced. Variability in EJC peak amplitudes is increased, compared to wild type. Transmission fidelity is lost. Calcium sensitivity is unaltered. MEJC frequency is not significantly altered, though amplitude is increased, perhaps because of increased quantity of neurotransmitter in some vesicles. Mutant synapses exhibit severe fatigue after prolonged stimulation. Synapses show decreased synaptic vesicle density and accumulate membrane-recycling intermediates. | |||
External Data
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| Linkouts | |||
Interactions
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Phenotypic Class
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Suppressed by | |||
Statement Reference stnA12, stnB12 has lethal | recessive | embryonic stage phenotype, suppressible by Scer\GAL44G/Syt1Scer\UAS.cLa stnA12, stnB12 has lethal | recessive | embryonic stage phenotype, suppressible by Syt1Scer\UAS.cLa/Scer\GAL41407 | |||
NOT suppressed by | |||
Statement Reference | |||
Other | |||
Statement Reference | |||
Phenotype Manifest In
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NOT Enhancer of | |||
Statement Reference | |||
Other | |||
Statement Reference | |||
Additional Comments
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Genetic Interactions
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Statement Reference stnA12 stnB12/Y ("stn13-120") males do not survive to adulthood. The lethality of stnA12 stnB12/Y ("stn13-120") animals is not rescued by expression of sytScer\UAS.cLa under the control of either Scer\GAL4elav-C155 or Scer\GAL4shi.PS. stnA12 stnB12 ("stn13-120") mutant embryos show a more than 90% reduction in FM1-43 dye uptake at the neuromuscular junction after stimulus compared to wild type. stnA12 stnB12 ("stn13-120") homozygotes show embryonic lethality. Expression of sytScer\UAS.cLa under the control of Scer\GAL41407 in this background results in approximately 98% of animals hatching at normal times, but they then die as first instar larvae. Expression of sytScer\UAS.cLa under the control of Scer\GAL44G in the stnA12 stnB12 background results in approximately 96% of embryos hatching, although hatching is delayed (animals hatch between 21 and 35 hours after fertilisation. These animals show adult viability. | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Fails to complement | |||
| Comments | Expression of the dicistronic P{UAS-stnAB.E} construct (which expresses stnAAB.Scer\UAS and stnBAB.Scer\UAS) under the control of either Scer\GAL4elav-C155 or Scer\GAL4shi.PS rescues the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of the dicistronic P{UAS-stnAB.E} construct (which expresses stnAAB.Scer\UAS and stnBAB.Scer\UAS) under the control of Scer\GAL4Mhc.PW does not rescue the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of stnBScer\UAS.cEa under the control of Scer\GAL4elav-C155 rescues the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of stnBScer\UAS.cEa under the control of Scer\GAL4Mhc.PW does not rescue the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of stnAScer\UAS.cEa under the control of Scer\GAL4elav-C155 does not rescue the lethality of stnA12 stnB12/Y ("stn13-120") animals. | ||
Stocks
( 0 ) | |||
Notes on Origin
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| Discoverer | Schalet. | ||
Induced with: stnB12. | |||
Comments
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Used in mosaic analysis to show that the "stn" product is not required for all cell types, but is required in the head for normal active behavior and in the thorax for motor coordination and posture. | |||
External Crossreferences & Linkouts
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| Other Crossreferences | |||
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Synonyms & Secondary IDs
( 5 ) | |||
| Reported As | |||
| Symbol Synonym | l(1)13-120 (Schalet, 1986, ) stn13-120 stn12 stn13-120 stnA12 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 11 ) | |||
| Research paper |
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| Abstract |
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Recent Updates
External Crossreferences & Linkouts