A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\ttk69.Scer\UAS

General Information
SymbolDmel\ttk69.Scer\UASSpeciesD. melanogaster
NameFlyBase IDFBal0127855
Feature typealleleAssociated geneDmel\ttk
Allele class
Mutagenin vitro construct - regulatory fusion
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Description
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FB2013_03
FB2013_02
Controlled Vocabulary Terms
eye
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 /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Construct: Scer\UAS regulatory sequences drive expression of a full length ttk69 cDNA.
Carried in construct
Cytology
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sensory mother cell & dorsal mesothoracic disc, with Scer\GAL4Bx-MS1096
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Statement
Reference
Expression of ttk[69.Scer\UAS] under the control of Scer\GAL4[GMR.PF] causes a distorted eye morphology characterized by disorganised facets and a loss of bristles. The cone cell pattern in the ommatidium of 40hr old pupal eye discs is also severely disrupted. The photoreceptor pattern is severely disrupted.
When ttk69.Scer\UAS is driven by Scer\GAL4Bx-MS1096 the wing blade area is reduced and all sensilla are removed except the ventral mechanosensory bristles. Sensory organ precursors are ablated in the wing disc.
Expression of ttk69.Scer\UAS under the control of Scer\GAL4GMR.PF abolishes the second mitotic wave in the eye disc. The proportion of cells behind the furrow in G2 is increased in these discs compared to wild type.
Expression of ttk69.Scer\UAS under the control of Scer\GAL4elav-C155 results in pathfinding and fasciculation defects in the central nervous system (CNS). The longitudinal fascicles are disorganised and the intersegmental nerve is misrouted and often fails to exit the CNS. Organisation of the peripheral nervous system is unaffected. Expression of ttk69.Scer\UAS under the control of Scer\GAL4Kr.PM inhibits normal glial development. Longitudinal glia are ablated when ttk69.Scer\UAS is expressed under the control of Scer\GAL4sca-537.4. The number of longitudinal glia is reduced when ttk69.Scer\UAS is expressed under the control of Scer\GAL4MZ1580. The normal BrdU incorporation in the ventral neuroectoderm is inhibited in embryos expressing ttk69.Scer\UAS under the control of Scer\GAL4Kr.PM.
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Reference
Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, ttk69.Scer\UAS has visible phenotype, non-suppressible by Ubp64E[+]/Ubp64ERev
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Reference
Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, ttk69.Scer\UAS has eye phenotype, non-suppressible by Ubp64E[+]/Ubp64ERev
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Statement
Reference
One copy of Ubp64E[Δ1] strongly suppresses the adult eye morphology phenotype seen when ttk[69.Scer\UAS] is expressed under the control of Scer\GAL4[GMR.PF]. The cone cell disruption see in pupal eye discs is also suppressed, as is the disruption to the photoreceptor pattern. One copy of Ubp64E[Rev] is unable to suppress the adult eye morphology phenotype seen when ttk[69.Scer\UAS] is expressed under the control of Scer\GAL4[GMR.PF]. The cone cell pattern disruption and loss of photoreceptors seen in pupal ommatidia is also unaffected. Co-expression of ttk[69.Scer\UAS] and Ubp64E[Scer\UAS.cBa] under the control of Scer\GAL4[GMR.PF] causes dramatically defective eye development, more severe than is seen when either transgene is expressed alone. The cone cell disruption seen in the ommatidia of pupal eye discs is also enhanced, as is the disruption to the photoreceptor pattern. Expression of Ubp64E[C405A.Scer\UAS] does not enhance the adult eye phenotypes seen when ttk[69.Scer\UAS] is expressed under the control of Scer\GAL4[GMR.PF]. The cone cell and photoreceptor disruption seen in the ommatidia of pupal eye discs is also unaffected.
Coexpression of stgScer\UAS.cNa completely rescues the second mitotic wave in eye discs expressing ttk69.Scer\UAS under the control of Scer\GAL4GMR.PF.
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Reported As
Symbol Synonym
ttk69.Scer\UAS
 
Name Synonym
Secondary FlyBase IDs
hide References ( 5 )
Research paper
Bajpe et al., 2008, Mol. Cell. Biol. 28(5): 1606--1615
Deubiquitylating enzyme UBP64 controls cell fate through stabilization of the transcriptional repressor tramtrack. [FBrf0204221]
Audibert et al., 2005, Development 132(10): 2287--2297
Cell cycle diversity involves differential regulation of Cyclin E activity in the Drosophila bristle cell lineage. [FBrf0187449]
Badenhorst et al., 2002, Mech. Dev. 117(1-2): 87--101
Tramtrack co-operates to prevent inappropriate neural development in Drosophila. [FBrf0152198]
Baonza et al., 2002, Nat. Cell Biol. 4(12): 976--980
Pointed and Tramtrack69 establish an EGFR-dependent transcriptional switch to regulate mitosis. [FBrf0155467]
Badenhorst, 2001, Development 128(20): 4093--4101
Tramtrack controls glial number and identity in the Drosophila embryonic CNS. [FBrf0139635]