A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\loqsf00791

General Information
SymbolDmel\loqsf00791SpeciesD. melanogaster
NameFlyBase IDFBal0161104
Feature typealleleAssociated geneDmel\loqs
Map ( GBrowse ) Untitled Document detailed view FBti0041938 FBti0124776_1 FBti0124776_2
Allele classhypomorphic allele - genetic evidence
MutagenpiggyBac transposase
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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
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Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Insertion 57bp upstream of the loqs transcription start site.
The insertion of a piggybac element within the first exon and 221 nucleotides upstream of the translational start codon of the loqs gene.
Caused by insertion
Cytology
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Statement
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loqs[f00791] mutant flies have a significantly shortened lifespan and show late-onset brain morphological deterioration. The brains of young adults appear normal, but by 25 days the flies have developed large vacuoles in the retina and lamina of the brain.
loqs[f00791] mutants display a reduction in dsRNA processing and a subsequent ~60% reduction in siRNA levels.
The longitudinal and commissural axon structures of the central nervous system are disrupted in homozygous embryos. Approximately 70% of homozygotes die before adulthood, and surviving males have reduced fertility and surviving females are sterile. Surviving adults are often stuck in the food. Homozygous adults have significantly reduced locomotor activity compared to controls.
loqs[f00791]/loqs[KO] females have an average of 0.5 germline stem cells (GSCs) per germarium at 10 days after eclosion, compared to an average of 2-3 GSCs per germarium in wild-type females at this age. Differentiated cystoblasts with posterior-positioned fusomes are often seen at the normal location of GSCs in the germaria of loqs[f00791]/loqs[KO] females.
loqs[f00791] mutants exhibit minimal disruption to the eye.
Only 17% of embryos derived from homozygous males mated to wild-type females hatch. Mutant males contain crystals of Ste protein in their testes. Mutant females have small ovaries and are completely sterile, failing to lay any eggs. The mutant ovarioles contain a smaller than normal germarium and contain only 2 or 3 previtellogenic egg chambers and a late-stage egg chamber (in contrast to the developmentally ordered array of 6-8 egg chambers seen in wild-type ovarioles). The mutant germarium contains only a few germ-line cells, which are not organised into distinct cysts. Spectrosomes can not be detected in the mutant germaria of 3-4 day old females, suggesting that no stem cells remain in these flies. The follicle cell layer is significantly reduced compared to wild-type. Mature oocytes in the mutant ovarioles have normal dorsal appendages.
loqsf00791 mutant females are completely sterile while males are approximately 60-70% sterile when compared with the control crosses between heterozygous and wild-type flies. Although mutant testes appear normal, mutant ovaries contain a few maturing egg chambers and a shriveled germarium with few healthy germline stem cells. The mutant ovary does not sustain continuous egg chamber production since germline stem cells can not be properly maintained.
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Reference
loqs[+]/loqsf00791 is a suppressor of male germline cell phenotype of maelM391/Df(3L)79E-F
loqsf00791/r2d21 is a suppressor | partially of eye phenotype of wIR.GMR
loqsf00791 is a suppressor | partially of eye phenotype of wIR.GMR
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Statement
Reference
loqs[f00791] mutant flies carrying two copies of w[IR.GMR] exhibit impaired w silencing and display orange-red eyes. loqs[f00791] r2d2[1] double mutant flies carrying two copies of w[IR.GMR] exhibit impaired w silencing and display orange-red eyes. loqs[f00791] r2d2[1] double mutants display a reduction in dsRNA processing and a subsequent ~80% reduction in siRNA levels.
The differentiation defects seen in the testes of mael[M391]/Df(3L)79E-F males are partially rescued by loqs[f00791]/+.
The germ cell tumour phenotype seen in bam[unspecified] females is not suppressed by loqs[f00791]/loqs[KO]. The double mutant germaria retain germline stem cells.
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 enhanced in a loqs[f00791] background, resulting in a severely degenerated eye with complete loss of pigmentation. Eye degeneration due to expression of Hsap\MJD[fl.Q84.Scer\UAS.T:Hsap\MYC] in the eye (under the control of Scer\GAL4[GMR.PF]) is enhanced in a loqs[f00791] background, resulting in dramatically reduced retinal thickness. Eye degeneration due to expression of Hsap\MAPT[Scer\UAS.cWa] in the eye (under the control of Scer\GAL4[GMR.PF]) is enhanced in a loqs[f00791] background. Eye degeneration due to expression of Hsap\MAPT[R406W.Scer\UAS] in the eye (under the control of Scer\GAL4[GMR.PF]) is enhanced in a loqs[f00791] background.
The silencing of the w gene seen in flies carrying P{GMR-wIR} is less efficient if the flies are also homozygous for loqsf00791; flies carrying two copies of P{GMR-wIR} and homozygous for loqsf00791 do not have completely white eyes (in contrast to flies carrying two copies of P{GMR-wIR} in a wild-type background).
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Rescued by
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Comments
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Bloomington
Harvard
Kyoto
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Discoverer
Separable from: a second mutation on the chromosome. The loqs[f00791] mutation does not cosegregate with the female sterility of the "f00791" chromosome.
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Precise excision of the insertion reverts the female sterile phenotype.
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hide Synonyms & Secondary IDs ( 6 )
Reported As
Symbol Synonym
R3D1f00791
Name Synonym
Secondary FlyBase IDs
hide References ( 21 )
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hide Recent research papers ( 4 )
Fukunaga et al., 2012, Cell 151(3): 533--546
Dicer Partner Proteins Tune the Length of Mature miRNAs in Flies and Mammals. [FBrf0219804]
Liu et al., 2012, Nature 482(7386): 519--523
The microRNA miR-34 modulates ageing and neurodegeneration in Drosophila. [FBrf0217556]
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]
Liu et al., 2011, Curr. Biol. 21(22): 1888--1893
The Exoribonuclease Nibbler Controls 3' End Processing of MicroRNAs in Drosophila. [FBrf0216782]