A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\lwr05486

General Information
SymbolDmel\lwr05486SpeciesD. melanogaster
NameFlyBase IDFBal0008090
Feature typealleleAssociated geneDmel\lwr
Also Known Asl(2)05486, lwr5486
Map ( GBrowse ) Untitled Document detailed view FBti0009117_2 FBti0009117_1 FBti0047453 FBti0072164 FBti0004244_2 FBti0004244_1
Allele classloss of function allele, hypomorphic allele - genetic evidence
MutagenP-element activity
hide Recent Updates
Description
What does this section display?
This section contains items that were added to this record for each release. It currently only tracks new links between this FlyBase report and other FlyBase data classes (e.g. genes, references, stocks) or controlled vocabulary terms (e.g. GO, anatomy terms).
What does this section not display?
This section does not currently display links that were removed or gene model changes.
Update Feed
Click the icon below to subscribe to this FlyBase record and receive updates automatically through your feed reader.
FB2013_03
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Nature of the Allele
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
P{PZ} insertion in the 5' untranslated region.
P{PZ} is inserted into the 5' UTR of lwr.
Caused by insertion
Cytology
hide Phenotypic Data
hide Phenotypic Class
hide Phenotype Manifest In
hide Detailed Description
Statement
Reference
No defects are seen in axon pruning during metamorphosis, though a severe proliferation defect is seen when somatic clones are made in the neuroblast.
Embryos transheterozygous for lwr05486 and lwr02858 show cuticle patterns resembling those of lwr118 homozygotes and of lwr05486/lwr118 transheterozygotes: a phenotype intermediate between the bcd and the hb mutant phenotypes. bcd protein is retained in the cytoplasm of lwr05486/lwr02858 transheterozygotes and lwr05486 homozygotes.
hide External Data
Linkouts
hide Interactions
hide Phenotypic Class
hideEnhancer of
Statement
Reference
hideSuppressor of
Statement
Reference
hideOther
Statement
Reference
hide Phenotype Manifest In
hideEnhancer of
Statement
Reference
hideNOT Enhancer of
Statement
Reference
lwr05486, smt3k06307, smt3[+], lwr[+] is a non-enhancer of eye phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, p53Scer\UAS.Ex
hideSuppressor of
Statement
Reference
lwr05486/lwr[+] is a suppressor | partially of meiosis & nuclear chromosome | female phenotype of mei-2186
lwr05486/lwr[+] is a suppressor of meiosis & nuclear chromosome | female phenotype of ncdD/ncd1
lwr05486/lwr[+] is a suppressor of meiosis & nuclear chromosome | female phenotype of nod2/noda
lwr05486/lwr[+] is a suppressor of meiosis & nuclear chromosome | female phenotype of nodDTW
lwr05486 is a suppressor | partially of meiosis & nuclear chromosome | female phenotype of AxsD
lwr05486 is a suppressor of meiosis & nuclear chromosome | female phenotype of mei-2181, nodDTW
lwr05486 is a suppressor of oocyte & spindle phenotype of mei-2181, nodDTW
lwr05486 is a suppressor of phenotype of nodDTW
hideNOT Suppressor of
Statement
Reference
lwr05486, smt3k06307, smt3[+], lwr[+] is a non-suppressor of eye phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, p53Scer\UAS.Ex
lwr05486/lwr[+] is a non-suppressor of eye phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, p53Scer\UAS.Ex
hideOther
Statement
Reference
hide Additional Comments
hide Genetic Interactions
Statement
Reference
A loss of heterozygosity assay, using mwh[1] as a marker, reveals that a lwr[05486] heterozygous background increases the number of mwh[1] clones after irradiation with 250 rad of X-rays, in p53[5A-1-4] mutants. The rough eye phenotype found at 29[o]C in flies expressing p53[Scer\UAS.Ex] under the control of Scer\GAL4[GMR.PF] is not affected by a lwr[05486] heterozygous background nor in a lwr[05486]-smt3[k06307] transheterozygous background.
lwr[05486]/Df(2L)32FP-5 double heterozygotes show a reduction in wing size (by 10%) compared to wild type.
The transheterozygote lwr05486/smt304493 suppresses the mod(mdg4)ul suppression of the ct6 jagged wing phenotype, leading to a more jagged and discontinuous wing phenotype. The phenotype is also particularly pronounced in females, although it is detectable in both sexes. The transheterozygote lwr05486/smt304493 suppresses the mod(mdg4)ul suppression of the y2 cuticle phenotype, leading to a lighter coloration of the abdomen (due to a reduction in y expression).These phenotypic changes occur in approximately 30% of the mutant flies, with the remaining 70% displaying a continuum of less-pronounced effect. The phenotype is also particularly pronounced in females, although it is detectable in both sexes.
lwr05486 dominantly suppresses the nondisjunction phenotype of nodDTW/+ females. noda/FM7a nod2 female nondisjunction is dominantly suppressed by lwr05486. 4th, but not X chromosome disjunction is suppressed in mei-2186 females if they also carry lwr05486/+. 4th, but not X chromosome disjunction is suppressed in AxsD females if they also carry lwr05486. ncd1/ncdD female X and 4th chromosome nondisjunction is dominantly suppressed by lwr05486. nodDTW mei-2181 double homozygous females show 60% X chromosome nondisjunction and 63% 4th chromosome nondisjunction. Oocyte spindles are often frayed or oddly shaped, or multiple spindles are present. These defects are suppressed by lwr05486/+.
A lwr[05486] mutant background does not affect the extent of ectopic wing veins or eye roughening seen in Scer\GAL4[GMR.PF] Cbl[Dv.Scer\UAS] mutants.
hide Xenogenetic Interactions
Statement
Reference
hide Complementation & Rescue Data
Complements
Partially complements
Fails to complement
Rescued by
Comments
Percent hatchability of embryos produced from a cross between lwr05486 and lwr02858 is 75%, whereas hatchability from a cross between ush2 and lwr02858 is 90%.
hide Stocks ( 1 )
Bloomington
hide Notes on Origin
Discoverer
A. Spradling.
hide Comments
Excision of the P{PZ} element can revert the mutant phenotype.
Most excisions of the P{PZ} element are homozygous viable and no longer suppress nodDTW. Lethal excision alleles remain suppressors.
Complements: ex01270. Complements: ds05142. Complements: Gsc05341. Complements: α-Adaptin06694. Complements: Sk06101. Complements: l(2)k08915k08915. Complements: l(2)k09610k09610. Complements: Nlek13714.
hide External Crossreferences & Linkouts
Other Crossreferences
Linkouts
hide Synonyms & Secondary IDs ( 6 )
Reported As
Symbol Synonym
l(2)0548605486
 
lesswrightr05486
Name Synonym
Secondary FlyBase IDs
hide References ( 17 )
Research paper
Pardi et al., 2011, Acta biol. hung. 62(4): 397--412
In vivo effects of abolishing the single canonical sumoylation site in the C-terminal region of Drosophila p53. [FBrf0216737]
Sánchez et al., 2010, J. Biol. Chem. 285(33): 25841--25849
Sumoylation Modulates the Activity of Spalt-like Proteins during Wing Development in Drosophila. [FBrf0211449]
Simonsen et al., 2007, Genetics 176(2): 1283--1297
Genetic modifiers of the Drosophila blue cheese gene link defects in lysosomal transport with decreased life span and altered ubiquitinated-protein profiles. [FBrf0201586]
Capelson and Corces, 2006, EMBO J. 25(9): 1906--1914
SUMO conjugation attenuates the activity of the gypsy chromatin insulator. [FBrf0193462]
Casso et al., 2005, Genetics 170(1): 139--148
Drosophila signal peptide peptidase is an essential protease for larval development. [FBrf0188526]
Watts et al., 2003, Neuron 38(6): 871--885
Axon pruning during Drosophila metamorphosis: evidence for local degeneration and requirement of the ubiquitin-proteasome system. [FBrf0161044]
Bhaskar et al., 2002, Mol. Cell. Biol. 22(2): 492--504
Conjugation of smt3 to dorsal may potentiate the Drosophila immune response. [FBrf0141657]
Apionishev et al., 2001, Genes Cells 6(3): 215--224
The Drosophila UBC9 homologue lesswright mediates the disjunction of homologues in meiosis I. [FBrf0134637]
Robertson et al., 2000, Oncogene 19(29): 3299--3308
A Drosophila analogue of v-Cbl is a dominant-negative oncoprotein in vivo. [FBrf0130045]
Spradling et al., 1999, Genetics 153(1): 135--177
The Berkeley Drosophila genome project gene disruption project. Single P-element insertions mutating 25% of vital Drosophila genes. [FBrf0111489]
Epps and Tanda, 1998, Curr. Biol. 8(23): 1277--1280
The Drosophila semushi mutation blocks nuclear import of bicoid during embryogenesis. [FBrf0105226]
Supplementary material
Epps and Tanda, 1998, Curr. Biol. 8(23):
The Drosophila semushi mutation blocks nuclear import of bicoid during embryogenesis. [FBrf0107698]
Personal communication to FlyBase
Beaton, 1999.12.12, Alleles of the lines in the P-element paper.
Alleles of the lines in the P-element paper. [FBrf0125032]
Rasooly, 1997.4.18, [title not yet available]
[title not yet available] [FBrf0093832]
Meister and Braun, 1995.10, lacZ expression patterns for P{} insertions at Bloomington.
lacZ expression patterns for P{} insertions at Bloomington. [FBrf0083714]
BDGP Project Members, 1994-1999, BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file)
BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file) [FBrf0067338]
Abstract
Apionishev and Rasooly, 1997, A. Dros. Res. Conf. 38: 171A
Genetic characterization of the suppressing activities of lesswright, a dominant modifier of nodDTW. [FBrf0092090]