A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\CrebBS162

General Information
SymbolDmel\CrebBS162SpeciesD. melanogaster
NameFlyBase IDFBal0006239
Feature typealleleAssociated geneDmel\CrebB
Also Known AsS162, DCREBS162, CrebBS162, CrebB-17AS162
Allele class
Mutagenethyl methanesulfonate
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Description
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FB2013_03
Genes
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
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Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
Associated Sequence Data
DDBJ /
EMBL /
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Protein sequence
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Nature of the lesion
Statement
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Cytology
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Statement
Reference
There is a significant decrease in synaptic bouton numbers at larval neuromuscular junctions (NMJs), compared with wild-type, in CrebB-17A[S162] mutants. Heterozygous CrebB-17A[S162] larvae have normal NMJs.
Homozygous CrebB-17A[S162] mutants are lethal. A single copy of CrebB-17A[S162] does not cause any lethality.
CrebB-17AS162, though lethal, is not completely penetrant, less than 0.5% of flies survive to adulthood. These escapers are about three quarters the size of wild type flies, but otherwise normal in appearance. Of 34 mutant flies tested for circadian locomotor activity, 13 (38%) were arrhythmic and the rest showed a short period averaging 22.8 hours.
Germline clones demonstrate no maternal effect. Zygotic lethality acts in the third larval instar stage.
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Reference
CrebBS162/CrebB-17A[+] is a non-suppressor of viable phenotype of Hsap\HTTQ22.ex1p.Scer\UAS, Scer\GAL4elav-C155
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Statement
Reference
Heterozygosity for both CrebB-17A[S162] and Df(1)Exel9051 results in a significant reduction in neuromuscular junction (NMJ) growth.
A CrebB-17A[S162] background suppresses the rough eye phenotype found in TORC[Scer\UAS.cWa]-expressing (under the control of Scer\GAL4[GMR.PF]) flies.
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Statement
Reference
The survival rate of flies expressing Hsap\HD[Q48.ex1p.Scer\UAS] in the nervous system (under the regulation of Scer\GAL4[elav-C155]) is sensitive to the gene dosage of CrebB-17A[S162] flies. A CrebB-17A[S162] heterozygous background more than doubles the lethality of Hsap\HD[Q48.ex1p.Scer\UAS] flies compared to flies expressing Hsap\HD[Q48.ex1p.Scer\UAS] alone (under the control of Scer\GAL4[elav-C155]). Addition of a heterozygous CrebB-17A[S162] background to CrebB-17A[+tIa] Hsap\HD[Q48.ex1p.Scer\UAS] (Scer\GAL4[elav-C155]) flies reduces the survival rate slightly, although lethality is not as high as in Hsap\HD[Q48.ex1p.Scer\UAS] (Scer\GAL4[elav-C155]) flies. The survival rate of flies expressing Hsap\HD[Q22.ex1p.Scer\UAS] in the nervous system (under the regulation of Scer\GAL4[elav-C155]) is not sensitive to the gene dosage of CrebB-17A[S162] flies. Homozygous CrebB-17A[S162] flies expressing Hsap\HD[Q48.ex1p.Scer\UAS] under the control of Scer\GAL4[elav-C155] are lethal. Addition of the CrebB-17A[+t.STOP] transgene to homozygous CrebB-17A[S162] flies expressing Hsap\HD[Q48.ex1p.Scer\UAS] under the control of Scer\GAL4[elav-C155] results in an approximate 1% survival rate.
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Rescued by
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Comments
Lethality can be almost fully rescued by an induced transgene carrying CrebB-17A, partial rescue is achieved with the non-induced transgene. Interpretation of rescue experiments is complicated as background genetic variability also gives partial rescue.
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Bloomington
Kyoto
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hide Synonyms & Secondary IDs ( 10 )
Reported As
Symbol Synonym
creb B-17AS162
DCREBS162
l(1)17Af1
 
l(1)S162
 
Name Synonym
Secondary FlyBase IDs
hide References ( 12 )
Research paper
Chen and Ganetzky, 2012, J. Cell Biol. 196(4): 529--543
A neuropeptide signaling pathway regulates synaptic growth in Drosophila. [FBrf0217500]
Kang et al., 2011, PLoS ONE 6(12): e29800
Novel Cytochrome P450, cyp6a17, Is Required for Temperature Preference Behavior in Drosophila. [FBrf0217065]
Fox et al., 2010, J. Cell Biol. 191(3): 479--492
The CrebA/Creb3-like transcription factors are major and direct regulators of secretory capacity. [FBrf0212217]
Iijima-Ando et al., 2009, PLoS ONE 4(12): e8310
Mitochondrial mislocalization underlies Abeta42-induced neuronal dysfunction in a Drosophila model of Alzheimer's disease. [FBrf0209556]
Wang et al., 2008, Cell Metab. 7(5): 434--444
The insulin-regulated CREB coactivator TORC promotes stress resistance in Drosophila. [FBrf0204686]
Iijima-Ando et al., 2005, Proc. Natl. Acad. Sci. U.S.A. 102(29): 10261--10266
cAMP-response element-binding protein and heat-shock protein 70 additively suppress polyglutamine-mediated toxicity in Drosophila. [FBrf0188259]
Kiger et al., 2001, Proc. Natl. Acad. Sci. U.S.A. 98(18): 10190--10195
Hemocytes are essential for wing maturation in Drosophila melanogaster. [FBrf0138518]
Belvin et al., 1999, Neuron 22(4): 777--787
The Drosophila dCREB2 gene affects the circadian clock. [FBrf0108141]
Eberl et al., 1992, Genetics 130: 569--583
Genetic and developmental analysis of polytene section 17 of the X chromosome of Drosophila melanogaster. [FBrf0056238]
Review
Stanewsky, 2003, J. Neurobiol. 54(1): 111--147
Genetic analysis of the circadian system in Drosophila melanogaster and mammals. [FBrf0155881]
Personal communication to FlyBase
Popodi et al., 2010-, Small X duplications for the stock center collection.
Small X duplications for the stock center collection. [FBrf0210621]
Abstract
Yin, 1997, A. Rep. Cold Spring Harbor Lab. 1996: 174--177
Long-term memory formation in Drosophila. [FBrf0098128]