A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Gene Dmel\flam

General Information
SymbolDmel\flamSpeciesD. melanogaster
NameflamencoAnnotation symbol
Feature typegeneFlyBase IDFBgn0005628
Gene Model StatusUnannotated Stock availability 2 publicly available
Genomic Location
Chromosome (arm)Recombination map1-
Cytogenetic map20A1-20A2Sequence location
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Automatically generated summary

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The gene flamenco is referred to in FlyBase by the symbol Dmel\flam (FBgn0005628). It is a gene from Drosophila melanogaster. Its molecular function is unknown. There is experimental evidence that it is involved in the biological process: ovarian follicle cell development; oogenesis; male courtship behavior. 23 alleles are reported. The phenotypes of these alleles are annotated with: ovariole; egg; ovary; germline cell; egg chamber; dorsal appendage; nurse cell. It has no annotated transcripts. Gene has not been localized to the genome sequence.

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FB2011_10
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FB2012_01
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FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
20A1-20A2  
Left limit from inclusion within Df(1)R20 (FBrf0080334) Right limit from inclusion within Df(1)LB6 (FBrf0080334)  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
20A1-20A3  
(determined by in situ hybridisation)  
Experimentally Determined Recombination Data
Location
1-
 
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Right of (cM)
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Annotated Transcripts
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Allele
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Allele
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Allele of flamClassMutagenStocksKnown lesion
flamBG02658
1 --
flamKG00476
1 --
flam1118.R
0 --
flam1
0 --
flam20 --
flam2G
0 --
flam679-14a0 Yes
flam679-16a0 Yes
flam679-5b0 Yes
flamEY13P0 --
flamEY2P0 --
flamEY7P0 --
flamFM7c
0 --
flamMS
0 --
flamN
0 --
flamOR0 --
flamovoD1
0 --
flampy+P0 --
flamRevR
0 --
flamSS0 --
flamsu(f)0 --
flamvg0 --
flamyw0 --
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Allele of flamClassMutagenStocksKnown lesion
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Not disrupted in
Disrupted in
Duplicated in
Not duplicated in
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Transgenic Constructs
Type of construct
Name
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Type of insertions
Name
Expression data
insertion of enhancer trap
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Molecular Function ( 0 terms)
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inferred from mutant phenotype
inferred from mutant phenotype
Cellular Component ( 0 terms)
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flam allele
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Bloomington
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Additional comments
"DIP1" does not correspond to the "flam" locus.
"flam" appears to map outside the region controlling ZAM and Idefix mobilisation ("COM").
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The flam locus corresponds to a piRNA cluster.
The proportion of normally copulating males is reduced in flam mutants compared to wild type. This reduction is due to changes in male behaviour. The proportion of males that perform consecutive courtship stages is significantly lower than in wild type. The sequence and duration of some courtship stages (in particular, orientation and wing vibration) is altered in mutant flies.
In some stocks active gypsy elements are found restricted to the Y chromosome. The presence of flam alleles tends to be associated with the confinement of active gypsy elements to the Y chromosome. This might be a result of the female-specific effect of flam on gypsy activity.
Cell lines carrying the permissive flam1 allele accumulate many nuclear virus-like particles, cytoplasmic dense particles and cisternae filled with fibrous material. Two of three such cell lines have an increased copy number of the gypsy element.
gypsy virus-like particles (VLPs) accumulate inside flam1 follicle cells close to envelope-containing membranes.
The length of time the existence of endogenous genomic gypsy was accompanied by host-virus co-evolution is studied. Host-virus co-evolution probably led to the acquisition by flam gene of the ability to control gypsy multiplication.
The expression of gypsy encoded proteins is analysed to explore how gypsy is transmitted between generations. Assembly of gypsy particles is visualised in the follicle cells of flam females by electron microscopy, these observations provide the basis for a novel model to explain how gypsy is transmitted from generation to generation. gypsy virions appear to move through the perivitelline space during a brief developmental window and infect the oocyte, providing a mechanism to explain gypsy insertion in the next generation.
Multiplication of gypsy in the germline is under the control of flam.
gypsy can be transmitted from flam strains in which it transposes to strains devoid of functional elements by egg plasm transfer or growing "empty" larvae in the presence of homogenized pupae of the flam stock. Transposition of gypsy occurs only in the progeny of females homozygous for permissive alleles of flam, where gypsy transcripts are restricted to the somatic follicle cells in the ovaries. Infectious particles which then infect the oocyte are apparently produced in these cells.
Mature gypsy particles are produced in the context of the flam mutation, which derepresses gypsy env production.
Deletion of flam does not lead to lethality or other abnormality of the flies. The only effect is on deregulation of gypsy mobilization.
The chromosomal flam locus controls the infective properties of gypsy.
Production of the gypsy\env message and corresponding protein is strongly repressed by one copy of the non-permissive allele of flam, flamN. A less dramatic reduction in the accumulation of other transcripts and retrotranscripts is also observed. These effects correlate with the inhibition of gypsy transposition in the progeny of these females and is likely to be responsible for this phenomenon. The effects of flam on gypsy\env expression are restricted to the somatic follicle cells that surround the maternal germline.
Females homozygous for mutant flam allele show a very high rate of gypsy mobilisation, for example 10-15% reversion of ovoD1. gypsy transcript altered on a mutant flam background.
 
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hide Recent research papers ( 7 )
Handler et al., 2011, EMBO J. 30(19): 3977--3993
A systematic analysis of Drosophila TUDOR domain-containing proteins identifies Vreteno and the Tdrd12 family as essential primary piRNA pathway factors. [FBrf0216344]
Zamparini et al., 2011, Development 138(18): 4039--4050
Vreteno, a gonad-specific protein, is essential for germline development and primary piRNA biogenesis in Drosophila. [FBrf0214783]
Haase et al., 2010, Genes Dev. 24(22): 2499--2504
Probing the initiation and effector phases of the somatic piRNA pathway in Drosophila. [FBrf0212277]
Moshkovich and Lei, 2010, PLoS Genet. 6(3): e1000880
HP1 Recruitment in the Absence of Argonaute Proteins in Drosophila. [FBrf0210291]
Olivieri et al., 2010, EMBO J. 29(19): 3301--3317
An in vivo RNAi assay identifies major genetic and cellular requirements for primary piRNA biogenesis in Drosophila. [FBrf0212004]
Saito et al., 2010, Genes Dev. 24(22): 2493--2498
Roles for the Yb body components Armitage and Yb in primary piRNA biogenesis in Drosophila. [FBrf0212297]
Stefanov et al., 2010, Mol. Genet. Genomics 284(5): 373--381
Amplification of "defective" retrotransposon gtwin in D. melanogaster strain carrying large complex chromosomal aberration. [FBrf0212070]
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