A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\bskScer\UAS.cBa

General Information
SymbolDmel\bskScer\UAS.cBaSpeciesD. melanogaster
NameSaccharomyces cerevisiae UAS construct a of BoutrosFlyBase IDFBal0093136
Feature typealleleAssociated geneDmel\bsk
Allele class
Mutagenin vitro construct - regulatory fusion
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Description
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FB2013_03
FB2013_02
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Construct: Expression of bsk cDNA is governed by Scer\UAS regulatory sequences.
Carried in construct
Cytology
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Statement
Reference
Expression of bsk[Scer\UAS.cBa] under the control of Scer\GAL4[twi.PG] results in delayed or defective ventral furrow formation in a proportion of embryos.
Expression of bsk[Scer\UAS.cBa] under the control of Scer\GAL4[Ubx-lac1-Gal4] results in transformation of posterior peripodial membrane cells of the wing disc from a hexagonal shape into an elongated shape.
Expression of bsk[Scer\UAS.cBa] under the control of Scer\GAL4[Act] induces autophagy in clones in the larval fat body.
Expression of bsk[Scer\UAS.cBa] in the wing, under the control of Scer\GAL4[Bx-MS1096] results in mild or undetectable phenotypic changes.
Expression of bskScer\UAS.cBa under the control of Scer\GAL4ey.PH results in eyes that are smaller than wild type.
Overexpression of bskScer\UAS.cBa, under the regulation of Scer\GAL4ap-md544 has no effect on thorax closure.
Expression of bskScer\UAS.cBa under the control of Scer\GAL4GMR.PF does not affect eye development.
Flies expressing bskScer\UAS.cBa, under the control of Scer\GAL4arm.PS, show a decreased sensitivity to paraquat compared to wild-type flies.
Expression of bskScer\UAS.cBa under the control of Scer\GAL4elav-C155 has no effect on EJC amplitude (synaptic strength) and bouton number at the larval neuromuscular junction.
When expression is driven by Scer\GAL4hs.2sev, flies have rough eyes showing polarity phenotypes. Ommatidia are incorrectly rotated and sometimes exhibit the wrong chiral form.
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bskScer\UAS.cBa has eye phenotype, enhanceable by L2/L[+]
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The autophagy that is induced by expression of bsk[Scer\UAS.cBa] under the control of Scer\GAL4[Act] in clones in the larval fat body still occurs in an Atg13[Δ81] homozygous background.
Expression of bsk[Scer\UAS.cBa] under the control of Scer\GAL4[tub.PU] rescues both the shortened lifespan increased sensitivity to paraquat which is seen in CYLD[mr4] mutant adults (animals homozygous for Df(2L)CYLD[mr4] and carrying P{LX107} to rescue the function of CG13138 and nmd).
Simultaneous expression of bsk[Scer\UAS.cBa] with lkb1[Scer\UAS.cLa] (both under the control of Scer\GAL4[Bx-MS1096] strongly enhances the lkb1[Scer\UAS.cLa] phenotype, resulting in severe disruption in the structure and size of the wing blades.
Expression of bskScer\UAS.cBa under the control of Scer\GAL4ey.PH enhances the loss-of-ventral-eye phenotype to near complete loss in 39% of L2/+ flies.
The thoracic cleft formation observed in parkScer\UAS.T:Hsap\MYC overexpression mutants (Scer\GAL4ap-md544) is suppressed by co-expression of bskScer\UAS.cBa.
Expression of bskScer\UAS.cBa under the control of Scer\GAL4ptc-559.1 results in a significant but partial rescue of the dorsal closure defects seen in cno2 embryos. Co-expression of bskScer\UAS.cBa does not rescue the dorsal closure defects seen in embryos expressing RN17.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4ptc-559.1.
Coexpression of bskScer\UAS.cBa with Traf1EP578, under the control of Scer\GAL4GMR.PF, leads to an increase in the disturbance of the ommatidial array in the compound eye in comparison to the eye phenotype resulting from one copy overexpression of Traf1EP578. Coexpression of Traf2EP1516 with either bskScer\UAS.cBa, under the control of Scer\GAL4GMR.PF, does not affect the development of eyes.
The mutant dorsal appendage phenotype seen in bwk151/bwk08482 eggs is not significantly modified by expression of bskScer\UAS.cBa under the control of Scer\GAL4c415.
The proportion of eyaScer\UAS.cHa; Scer\GAL4dpp.PH flies with blistered wings (76%) is relatively unaffected by the presence of bskScer\UAS.cBa (82%), as is the proprotion with only mild wing defects 24% compared to 18%. (All data from experiments with a single, 'strong' P{UAS-eya.H} insertion; n=approximately 300 in each case).
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Bloomington
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hide Synonyms & Secondary IDs ( 3 )
Reported As
Symbol Synonym
bskScer\UAS.cBa
 
bskUAS.cBa
 
Name Synonym
Saccharomyces cerevisiae UAS construct a of Boutros
Secondary FlyBase IDs
hide References ( 19 )
Research paper
Gonda et al., 2012, PLoS ONE 7(7): e42369
Drosophila Heat Shock Response Requires the JNK Pathway and Phosphorylation of Mixed Lineage Kinase at a Conserved Serine-Proline Motif. [FBrf0219015]
Mathew et al., 2011, Mol. Cell. Biol. 31(24): 4978--4993
Role for traf4 in polarizing adherens junctions as a prerequisite for efficient cell shape changes. [FBrf0216703]
Tripura et al., 2011, Int. J. Dev. Biol. 55(6): 583--590
Regulation and activity of JNK signaling in the wing disc peripodial membrane during adult morphogenesis in Drosophila. [FBrf0216296]
Chang and Neufeld, 2009, Mol. Biol. Cell 20(7): 2004--2014
An Atg1/Atg13 complex with multiple roles in TOR-mediated autophagy regulation. [FBrf0207848]
Xue et al., 2007, Dev. Cell 13(3): 446--454
Tumor suppressor CYLD regulates JNK-Induced cell death in Drosophila. [FBrf0200559]
Lee et al., 2006, Cell Death Differ. 13(7): 1110--1122
JNK pathway mediates apoptotic cell death induced by tumor suppressor LKB1 in Drosophila. [FBrf0194576]
Singh et al., 2006, Development 133(23): 4771--4781
Lobe and Serrate are required for cell survival during early eye development in Drosophila. [FBrf0192707]
Cha et al., 2005, Proc. Natl. Acad. Sci. U.S.A. 102(29): 10345--10350
Parkin negatively regulates JNK pathway in the dopaminergic neurons of Drosophila. [FBrf0188253]
Boettner et al., 2003, Genetics 165(1): 159--169
The AF-6 homolog canoe acts as a Rap1 effector during dorsal closure of the Drosophila embryo. [FBrf0162150]
Cha et al., 2003, Mol. Cell. Biol. 23(22): 7982--7991
Discrete functions of TRAF1 and TRAF2 in Drosophila melanogaster mediated by c-Jun N-terminal kinase and NF-kappaB-dependent signaling pathways. [FBrf0167884]
Lee et al., 2003, Development 130(17): 4001--4010
blistery encodes Drosophila tensin protein and interacts with integrin and the JNK signaling pathway during wing development. [FBrf0160724]
Tran and Berg, 2003, Development 130(25): 6273--6282
bullwinkle and shark regulate dorsal-appendage morphogenesis in Drosophila oogenesis. [FBrf0167514]
Wang et al., 2003, Dev. Cell 5(5): 811--816
JNK signaling confers tolerance to oxidative stress and extends lifespan in Drosophila. [FBrf0167481]
Hsiao et al., 2001, Dev. Cell 1(1): 51--61
Eyes absent mediates cross-talk between retinal determination genes and the receptor tyrosine kinase signaling pathway. [FBrf0141456]
McEwen et al., 2000, Development 127(16): 3607--3617
The canonical Wg and JNK signaling cascades collaborate to promote both dorsal closure and ventral patterning. [FBrf0128573]
Weber et al., 2000, Development 127(16): 3619--3629
Jun mediates Frizzled-induced R3/R4 cell fate distinction and planar polarity determination in the Drosophila eye. [FBrf0128678]
Boutros et al., 1998, Cell 94(1): 109--118
Dishevelled activates JNK and discriminates between JNK pathways in planar polarity and wingless signaling. [FBrf0103240]
Supplementary material
Chang and Neufeld, 2009, Mol. Biol. Cell 20(7):
Supplemental Data. [FBrf0208115]
Letter
Sanyal et al., 2002, Nature 416(6883): 870--874
AP-1 functions upstream of CREB to control synaptic plasticity in Drosophila. [FBrf0147170]