A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\Dcr-2L811fsX

General Information
SymbolDmel\Dcr-2L811fsXSpeciesD. melanogaster
NameFlyBase IDFBal0156733
Feature typealleleAssociated geneDmel\Dcr-2
Also Known Asdcr2L811fsX, Dcr-2L811X, dicer-2L811fsX
Map ( GBrowse ) GBrowse View Helpdetailed view FBal0156733
Allele classloss of function allele
Mutagenethyl methanesulfonate
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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
References
sequence variant
comment=Leu 811 is replaced by FGIRSLCWIVAARRTPTWX.
evidence=experimental
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
The Leucine at residue 811 is replaced by FGIRSLCWIVAARRTPTWX.
Cytology
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Statement
Reference
More than 60% of cells in anaphase mutant wing discs contain lagging chromosomes.
Dcr-2[L811fsX]/+ significantly suppresses the position effect variegation of the Sb[1] allele that is seen in the T(2;3)Sb[V] chromosome. Dcr-2[L811fsX]/Dcr-2[R416X] suppresses the position effect variegation of the w gene that is seen in the In(1)w[m4] chromosome.
Homozygous projection neurons show normal dendrite and axon targeting.
Dcr-2[L811fsX] mutant germline stem cells (GSCs) do not exhibit any maintenance defects when clones are induced either during larval/pupal stages or during adult stages.
Mutant flies are more susceptible to infection with RNA viruses (Flock House virus, Drosophila C virus or Sindbis virus) than control flies.
Embryos derived from Dcr-2L811fsX mothers exhibit normal cellularization and net lipid-droplet transport.
Dcr-2L811fsX homozygous flies fail to produce siRNA from a transfected construct.
Mutant flies are hypersensitive to infection with Cricket Paralysis virus (CrPV); the median survival after inoculation with 350 TCID50 of CrPV is reduced compared to controls.
Dcr-2L811fsX flies show increased mortality and an increased level of viral accumulation following infection with both Flock house virus (FHV) and cricket paralysis virus (CrPV).
When Dcr-2L811fsX germ-line clones are made a normal progression of egg chambers is seen.
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Statement
Reference
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Statement
Reference
Dcr-2L811fsX is a suppressor of eye color defective phenotype of wIR.GMR
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Statement
Reference
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Statement
Reference
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hideSuppressed by
Statement
Reference
Dcr-2L811fsX, wIR.GMR has eye phenotype, suppressible by Dcr-2E1210V.t7.2
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Statement
Reference
Dcr-2L811fsX, wIR.GMR has eye phenotype, non-suppressible by Dcr-2E1371K.E1617K.t7.2
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Statement
Reference
hideSuppressor of
Statement
Reference
Dcr-2L811fsX is a suppressor of eye phenotype of wIR.GMR
Dcr-2L811fsX is a suppressor of pigment cell phenotype of wIR.GMR
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Statement
Reference
The eyes of w[dsRNA.GMR] transgenic female flies homozygous for Dcr-2[L811fsX] are similar to that of wild-type.
w[IR.GMR] eyes that are also homozygous for Dcr-2[L811fsX] show strong suppression of the pale eye colour phenotype.
Flies carrying w[IR.GMR] in which the eyes are homozygous for Dcr-2[L811fsX] have dark red eyes.
Flies carrying one copy of w[dsRNA.GMR] in a homozygous Dcr-2[L811fsX] background have red eyes.
Dcr-1[Q1147X] Dcr-2[L811fsX] double mutants show strong germline stem cell maintenance (GSC) defects when GSC clones are induced during late larval/early pupal stages.
Eye degeneration due to expression of Hsap\MJD[tr.Q78.Scer\UAS.T:Ivir\HA1] in the eye (under the control of Scer\GAL4[GMR.PF]) is unaffected by a Dcr-2[L811fsX] background.
The wing phenotype of sdFab-X flies is suppressed in sdFab-X;Dcr-2L811fsX flies.
A Dcr-2L811fsX/+ background partially suppresses the small eye phenotype that is seen when thdsRNA.Scer\UAS is expressed under the control of Scer\GAL4GMR.PF. Dcr-2L811fsX; Dcr-1Q1147X double mutants show no segment polarity defects.
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Statement
Reference
Zzzz\CAG[99.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] expression using Scer\GAL4[da.G32] in the presence of heterozygous Dcr-2[L811fsX] does not give significantly different phenotype severity compared to Zzzz\CAG[99.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] expression in a wild-type Dcr-2 background. Zzzz\CAG[rCUG.99.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] expression using Scer\GAL4[da.G32] in the presence of heterozygous Dcr-2[L811fsX] does not give significantly different phenotype severity compared to Zzzz\CAG[rCUG.99.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] expression in a wild-type Dcr-2 background.
Heterozygous Dcr-2[L811fsX] suppresses the eye-phenotype resulting from the co-expression of Zzzz\CAG[99.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] and Zzzz\CAG[rCUG.99.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[GMR.PF]. In addition, the overall disruption observed in patterning of the internal structure of the eye is significantly reduced in the presence of heterozygous Dcr-2[L811fsX] as revealed by sections through adult eyes.
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Comments
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Bloomington
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Discoverer
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hide Synonyms & Secondary IDs ( 13 )
Reported As
Symbol Synonym
dcr-2L811Ex
dcr-2L811fs
Dcr-2L811fsx
dicer-2L811fsX
Dicer-2L811fsX
Name Synonym
Suppressor(GMR-wIR)A293
Secondary FlyBase IDs
hide References ( 43 )
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hide Recent research papers ( 9 )
Fukunaga et al., 2012, Cell 151(3): 533--546
Dicer Partner Proteins Tune the Length of Mature miRNAs in Flies and Mammals. [FBrf0219804]
Lawlor et al., 2012, PLoS ONE 7(6): e38516
Ubiquitous Expression of CUG or CAG Trinucleotide Repeat RNA Causes Common Morphological Defects in a Drosophila Model of RNA-Mediated Pathology. [FBrf0218612]
Dufourt et al., 2011, DNA Res. 18(6): 451--461
Polycomb group-dependent, heterochromatin protein 1-independent, chromatin structures silence retrotransposons in somatic tissues outside ovaries. [FBrf0216699]
Harris et al., 2011, J. Cell Biol. 194(1): 77--87
Cargo sorting to lysosome-related organelles regulates siRNA-mediated gene silencing. [FBrf0214287]
Lawlor et al., 2011, Hum. Mol. Genet. 20(19): 3757--3768
Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases. [FBrf0215240]
Okamura et al., 2011, Mol. Cell. Biol. 31(4): 884--896
R2D2 Organizes Small Regulatory RNA Pathways in Drosophila. [FBrf0212879]
Pek and Kai, 2011, Proc. Natl. Acad. Sci. U.S.A. 108(29): 12007--12012
DEAD-box RNA helicase Belle/DDX3 and the RNA interference pathway promote mitotic chromosome segregation. [FBrf0214405]
Pek and Kai, 2011, Curr. Biol. 21(1): 39--44
A role for vasa in regulating mitotic chromosome condensation in Drosophila. [FBrf0212718]
Poulton et al., 2011, Development 138(9): 1737--1745
The microRNA pathway regulates the temporal pattern of Notch signaling in Drosophila follicle cells. [FBrf0213494]