A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\ttkp69.Scer\UAS

General Information
SymbolDmel\ttkp69.Scer\UASSpeciesD. melanogaster
NameFlyBase IDFBal0060851
Feature typealleleAssociated geneDmel\ttk
Allele class
Mutagenin vitro construct - regulatory fusion
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Description
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FB2013_03
FB2013_02
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Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
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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
Construct: cDNA clone expressing the p69 protein of ttk is cloned into vector pUAST.
Carried in construct
Cytology
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Statement
Reference
Follicular cells expressing ttk[p69.Scer\UAS] under the control of Scer\GAL4[e22c] are reduced in size.
Expression of ttk[p69.Scer\UAS] under the control of Scer\GAL4[lz-gal4] results in severely disrupted adult eyes that show scarring and lack ommatidial structures. In third instar larval eye discs ommatidia show reduced numbers of cone cells and R1, R6 and R7 photoreceptor cells. Expression of ttk[p69.Scer\UAS] under the control of Scer\GAL4[GMR.PF] results in severely perturbed adult eyes, displaying no ommatidial structure. Ommatidia show reduced numbers of cone cells and R1, R6 and R7 photoreceptor cells.
Expression of ttk[p69.Scer\UAS] under the control of Scer\GAL4[btl.PS] results in impaired tracheal branch fusion.
When expression is driven by Scer\GAL4c739, ttkp69.Scer\UAS shows a mushroom body Class I phenotype; neuron number reduced. This phenotype is similar to, but less extreme than, that caused by ttkUY181 driven by Scer\GAL4c739. Loss of neurons is not accompanied by increase in number of glial cells.
When Scer\GAL4c527 is expressed under the control of Scer\GAL4c527 in third instar larvae, defects are seen in glial cell migration in the developing eye. In about 20% of these animals surface glial cells do not enter the eye disc and R cell axons fail to enter the optic stalk forming a mass of R cell axons in the basal region of the disc. In the remaining larvae, fewer surface glial cells are found in the eye disc. In these discs R cell axons project into the optic stalk, but are highly disorganised.
Flies expressing ttkp69.Scer\UAS under the control of Scer\GAL4cb12, Scer\GAL4cb19, Scer\GAL4cb35, Scer\GAL4cb36, Scer\GAL4cb37 or Scer\GAL4cb38 are moderately viable. Flies expressing ttkp69.Scer\UAS under the control of Scer\GAL4cb05 or Scer\GAL4cb23 are viable at 18oC.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4ey.PB results in deletion of the eye.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4dpp.blk1 affects furrow reincarnation but not birth in the eye disc.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4Eq1 results in a lack of most microchaetae.
Scer\GAL4Kr.PM-mediated expression leads to a partial block of neuronal development in the PNS and CNS. Scer\GAL4sca-537.4-mediated expression impairs neuronal differentiation. In late stage 16/17 embryos cell death is observed.
Eyes are deformed, severely reduced in size and lack bristles, cone cells and photoreceptor cells in flies expressing ttkp69.Scer\UAS under the control of Scer\GAL4GMR.PF.
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Statement
Reference
ttkp69.Scer\UAS/Scer\GAL4Eq1 is a suppressor of mesothoracic tergum & microchaeta | ectopic phenotype of Scer\GAL4Eq1, phylScer\UAS.cPa
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Statement
Reference
Over-expression of lz[GMR.PD] in flies expressing ttk[p69.Scer\UAS] in under the control of Scer\GAL4[GMR.PF] partially suppresses the loss cone cells and R1, R6 and R7 photoreceptor cells.
Co-expression of repoScer\UAS.cYa and ttkp69.Scer\UAS under the control of Scer\GAL4sca-T3 results in a synergistic suppression of neuronal development in embryos.
Most notal microchaetae are missing in animals coexpressing phylScer\UAS.cPa and ttkp69.Scer\UAS under the control of Scer\GAL4Eq1.
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Rescues
Partially rescues
Comments
Expression of ttk[p69.Scer\UAS] under the control of Scer\GAL4[btl.PS] in ttk[D2-50] mutant animals rescues the tracheal intercalation defects. Terminal branch fusion defects of the lateral trunk are also rescued in these animals.
Short heat shocks and moderate temperatures in ttktwp/ttktwp, ttkp69.Scer\UAS Scer\GAL4hs.PB animals lead to significant partial rescue of dorsal appendage and chorion defects. Eggs are normal in shape and size and dorsal appendages are significantly longer than seen in the mutants alone. Longer heat shocks lead to a dramatic decline in rescue frequency accompanied by an increase in defects early in oogenesis.
Scer\GAL4sli.PS-mediated expression partially rescues the CNS phenotype with two copies of the construct.
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Bloomington
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hide Synonyms & Secondary IDs ( 2 )
Reported As
Symbol Synonym
ttkp69.Scer\UAS
 
ttkp69.UAS
 
Name Synonym
Secondary FlyBase IDs
hide References ( 15 )
Research paper
Boyle and Berg, 2009, Development 136(24): 4187--4197
Control in time and space: Tramtrack69 cooperates with Notch and Ecdysone to repress ectopic fate and shape changes during Drosophila egg chamber maturation. [FBrf0209360]
Li et al., 2009, Cell 137(2): 273--282
A microRNA imparts robustness against environmental fluctuation during development. [FBrf0207846]
Siddall et al., 2009, BMC Dev. Biol. 9: 64
Ttk69-dependent repression of lozenge prevents the ectopic development of R7 cells in the Drosophila larval eye disc. [FBrf0209609]
Araujo et al., 2007, Development 134(20): 3665--3676
Tramtrack regulates different morphogenetic events during Drosophila tracheal development. [FBrf0201143]
French et al., 2003, Dev. Biol. 253(1): 18--35
The Drosophila female sterile mutation twin peaks is a novel allele of tramtrack and reveals a requirement for Ttk69 in epithelial morphogenesis. [FBrf0155483]
Nicolai et al., 2003, J. Neurobiol. 57(3): 291--302
Gain-of-function screen identifies a role of the Src64 oncogene in Drosophila mushroom body development. [FBrf0167790]
Yuasa et al., 2003, Development 130(11): 2419--2428
Drosophila homeodomain protein REPO controls glial differentiation by cooperating with ETS and BTB transcription factors. [FBrf0158889]
Hummel et al., 2002, Neuron 33(2): 193--203
Temporal control of glial cell migration in the Drosophila eye requires gilgamesh, hedgehog, and eye specification genes. [FBrf0145174]
Merabet et al., 2002, Genetics 162(1): 189--202
A green fluorescent protein reporter genetic screen that identifies modifiers of Hox gene function in the Drosophila embryo. [FBrf0152032]
Ward et al., 2002, genesis 34(1-2): 46--50
GAL4 enhancer trap patterns during Drosophila development. [FBrf0152375]
Kumar and Moses, 2001, Cell 104(5): 687--697
EGF receptor and Notch signaling act upstream of Eyeless/Pax6 to control eye specification. [FBrf0134490]
Kumar and Moses, 2001, Development 128(14): 2689--2697
The EGF receptor and notch signaling pathways control the initiation of the morphogenetic furrow during Drosophila eye development. [FBrf0138358]
Pi et al., 2001, Development 128(14): 2699--2710
A dual function of phyllopod in Drosophila external sensory organ development: cell fate specification of sensory organ precursor and its progeny. [FBrf0138359]
Giesen et al., 1997, Development 124(12): 2307--2316
Glial development in the Drosophila CNS requires concomitant activation of glial and repression of neuronal differentiation genes. [FBrf0094782]
Li et al., 1997, Cell 90(3): 469--478
Photoreceptor cell differentiation requires regulated proteolysis of the transcriptional repressor tramtrack. [FBrf0098298]