A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Gene Dmel\vas

General Information
SymbolDmel\vasSpeciesD. melanogaster
NamevasaAnnotation symbolCG43081
Feature typeprotein_coding_geneFlyBase IDFBgn0262526
Gene Model StatusCurrent Stock availability 22 publicly available
Also Known AsVasa, CG3506, BG:DS00929.15, BG:DS00929.14, cgt
Genomic Location
Chromosome (arm)2LRecombination map
Cytogenetic map35C1-35C1Sequence location2L:15,061,656..15,074,311 [+]

Genomic Maps

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Automatically generated summary

See sections below for more information
The gene vasa is referred to in FlyBase by the symbol Dmel\vas (CG43081, FBgn0262526). It is a protein_coding_gene from Drosophila melanogaster. There is experimental evidence that it has the molecular function: protein binding; mRNA 3'-UTR binding; RNA binding. There is experimental evidence that it is involved in the biological process: mitotic chromosome condensation; meiotic sister chromatid cohesion, centromeric; positive regulation of translation; oogenesis; pole plasm assembly; dorsal appendage formation; pole plasm RNA localization; germarium-derived egg chamber formation. 92 alleles are reported. The phenotypes of these alleles are annotated with: multicellular structure; anatomical structure; organ system; abdominal segment; portion of tissue; acellular anatomical structure; oocyte nucleus; embryonic abdominal segment 1; extended germ band embryo; nuclear part; cytoplasmic part; abdominal segment 10; stage S9 oocyte; karyosome. It has 2 annotated transcripts and 2 annotated polypeptides. Protein features are: DEAD-like helicase; DNA/RNA helicase, DEAD/DEAH box type, N-terminal; Helicase, C-terminal; RNA helicase, ATP-dependent, DEAD-box, conserved site; RNA helicase, DEAD-box type, Q motif. Gene sequence location is 2L:15061656..15074311.

hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
vas: vasa (T. Schupbach)
exhibit a so-called "grandchildless-knirps" phenotype: all eggs lack polar granules and no pole cells are formed; most of the embyros show large deletions of abdominal segments, whereby anterior parts of segment A1 become fused to posterior parts of segment A8. Telson elements are always present and relatively normal. Eggs have abnormal shape. Analysis of germline clones indicates that the mutation is germline autonomous (Schupbach and Wieschaus, 1986, Dev. Biol. 113: 443-448). Homozygous vasa males cannot be distinguished from wild-type males in viability and fertility.
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Description
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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).
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FB2011_10
References
FB2012_01
Sequence features
References
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Detailed Mapping Data
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
35C1-35C1  
Limits computationally determined from genome sequence between P{lacW}Su(H)k07904 and P{EP}vigEP812&P{PZ}stc05441  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
35B10-35C1  
(determined by in situ hybridisation) 35C1--3 (determined by in situ hybridisation)  
35B-35B  
(determined by in situ hybridisation)  
35C-35C  
(determined by in situ hybridisation)  
35C-35C  
(determined by in situ hybridisation)  
35C-35C  
(determined by in situ hybridisation)  
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
cgt is genetically inseparable from vas.
hide Gene Model & Products
Please see the GBrowse view of Dmel\vas for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
detailed view FBtr0080722 FBtr0304855 FBtr0304854 FBtr0080721 FBtr0080720 FBtr0080719 FBtr0080718 FBtr0080703 FBtr0080702 FBtr0307486 FBpp0080281 FBpp0080277 FBpp0080280 FBpp0080279 FBpp0080278 FBpp0293394 FBpp0293395 FBpp0089099 FBpp0080263 FBpp0298821 FBti0124801 FBti0109303 FBti0028715 FBti0024164 FBti0109887 FBti0107315 FBti0012159 FBti0124802 FBti0010371 FBti0037897 FBti0143835 FBti0143536 FBti0008393 FBti0124803_1 FBti0124803_2 FBti0111772 FBti0029199 FBti0036129 FBti0010632 FBti0056933 FBti0038775 FBti0127631 FBti0024613 FBti0069951 FBti0056833 FBti0055414 FBti0030154 FBti0036055 FBti0124804_1 FBti0124804_2
Comments on Gene Model
Gene merge based on EST/cDNA data.
EST data suggest alternative transcripts with additional internal exons; inconclusive.
hide Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Associated CDS (aa)
FBtr0304854
 
  2285
  661
FBtr0304855
 
  3337
  1031
Additional Transcript Data & Comments
Reported size (kB)
4, 3 (northern blot); 2.0 (unknown)
2.2 (compiled cDNA)
Comments
External Data
Crossreferences
hide Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
vas-PA  
FBpp0293394  
72.3  
661  
5.34  
 
 
vas-PB  
FBpp0293395  
112.5  
1031  
5.66  
 
 
Additional Polypeptide Data & Comments
Reported size (kDa)
660 (aa); 72 (kD)
648 (aa); 72 (kD)
Comments
vas protein may be an ATP-dependent nucleic acid helicase.
External Data
Linkouts
Crossreferences
InterPro domains - A database of protein families, domains, and functional sites
hide Sequences Consistent with the Gene Model
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
hide Mapped Features
Mapped Features have been reorganized, please see this article for details.
Additional mapped features and mutations can be found on GBrowse or related reports.
Type
Symbol & Location
Additional Notes
References
hide External Data
Linkouts
Crossreferences
hide Expression Data
hideTranscript Expression
No Assay Recorded
Stage
Tissue/Position (including subcellular localization)
Reference
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
northern blot
Stage
Tissue/Position (including subcellular localization)
Reference
RT-PCR
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
vas expression is observed in male germ cells.
vas expression is observed in female germ cells.
Marker for
Subcellular Localization
CV Term
Notes
hidePolypeptide Expression
No Assay Recorded
Stage
Tissue/Position (including subcellular localization)
Reference
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
Comment:Probed with antibody to Bombyx vas.
Comment:Probed with antibody to Bombyx vas.
Additional Descriptive Data
vas protein is cytoplasmic within pole cells. In some cell types in ovaries and testes, vas protein distribution is perinuclear.
vas protein is concentrated in the form of polar granules at the posterior pole in early embryos. A low level of staining is also seen throughout the embryo during cleavage stages. vas protein is also present in egg chambers. Protein expression in mutants of vas, stau, osk, tud, vls, and BicD were studied.
The vas protein is expressed in germ cells at the larva/pupa transition, 108 hrs AEL.
vas protein in both late-stage oocytes and in early embryos is localized to the posterior pole, and thus differs from the uniform distribution of vas transcript at the same stage. In addition to late-stage oocytes, the vas protein is found in germline stem cells and nurse cells of ovaries. In adult males, the vas protein is present in male germline stem cells during early spermatogenesis.
germline cell
vas protein is detected in larval and pupal ovaries in the oogonial cells and their precursors. It is abundant in the germaria of adult ovaries and is also abundant in the pronurse cell nuclei in early stages of oogenesis. vas protein is transported to the oocyte starting in stage 8 and is concentrated at the posterior pole, although it is detectable at lower levels throughout the oocyte. vas protein is also detected in males in the larval spermatogonial cells and in cyst cells of the adult testis. In early cleavage stage embryos, a shallow posterior-anterior gradient of vas protein is seen with the highest concentration at the posterior pole. Later the pole cells stain heavily and the pole cell and subsequent gonadal expression persists throughout embryogenesis. In ovaries lacking tud, vls, nos, and pum, vas protein localizes to the posterior pole of the oocyte normally but in ovaries lacking osk and stau, vas protein fails to distribute asymmetrically. BicC mutations affect vas protein distribution while BicD mutations do not. capu and spir abolish localization of vas protein to pole cells. vas protein is detected in ovaries of egl, mus301, qua, Bic-F, mr, Fs(2)Y12, and vss mutant females.
vas protein is located at the posterior pole of early embryos. This posterior localization is abolished in mutants of stau, vas, spir, capu, and osk. Posterior localization of vas protein is less striking in tud and vls mutants than in wild type embryos and indistinguishable from wild type in nos and pum mutants.
Marker for
Subcellular Localization
CV Term
cytoplasm perinuclear space
Notes
hide High-Throughput Expression Data
or
Untitled Document detailed view TfIIS-RA vas-RB vas-RA vig-RB vig-RA vig-RC vig-RD CG15270-RB CG15270-RA CG15270-RC
See Gelbart and Emmert, 2010.10.13 for analysis details and data files for all genes.
modENCODE Temporal Expression Data (Graveley et al., 2011)
FlyAtlas Anatomical Expression Data (Chintapalli et al., 2007)
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hide Summary of Allele Phenotypes
Lethality
Allele
Sterility
Allele
Other Phenotypes
Allele
Phenotype manifest in
Allele
hide Classical Alleles ( 45 )
For All Classical Alleles Show

Allele of vasClassMutagenStocksKnown lesion
vas17 Yes
vasKG01651
2 --
vasRJ362 --
vasd040881 --
vasd097271 --
vasEY078161 Yes
vasMB11697
1 --
vasUM-8145-3
1 --
vasP808amorphic allele - genetic evidence0 Yes
vassolo-Z2-0198amorphic allele - genetic evidence0 Yes
vassolo-Z2-0338amorphic allele - genetic evidence0 Yes
vassolo-Z2-3534amorphic allele - genetic evidence0 Yes
vas004240 --
vas150 Yes
vas20 --
vas3loss of function allele0 Yes
vas3F
0 Yes
vas40 Yes
vas4C
0 Yes
vas50 Yes
vas6356-0010 Yes
vas6356-0050 Yes
vas60 Yes
vas7loss of function allele0 Yes
vas88c25
0 --
vasAQB30 --
vasAS
0 Yes
vasBC690 --
vasC920 --
vasd084080 --
vasD50 Yes
vasEP8120 Yes
vasETo140 --
vasG890 --
vasHE10 Yes
vask072330 Yes
vasKD
0 --
vasLYG2hypomorphic allele - genetic evidence0 Yes
vasM130 --
vasNP4680
0 --
vasPH1650 Yes
vasPW720 Yes
vasQS170 Yes
vasRG530 Yes
vasunspecified0 --
hide Alleles Carried on Transgenic Constructs ( 47 )
For All Alleles Carried on Transgenic Constructs Show

Allele of vasClassMutagenStocksKnown lesion
vasGD15561 Yes
vasGD160981 Yes
vasHM052391 Yes
vasHMS003731 Yes
vasHMS004311 Yes
vasKK1009291 Yes
vasC.solo.Scer\UAS.P\T.T:Avic\GFP-YFP.Venus
0 Yes
vasD554A.Scer\UAS.P\Tantimorphic allele - genetic evidence0 Yes
vasdel.10.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.11.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.12.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.13.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.14.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.15.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.16.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.17.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.18.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.19.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.2.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.20.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.21.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.22.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.23.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.3.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.4.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.5.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.6.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.7.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasdel.8.T:Avic\GFP-EGFP,T:Ivir\HA10 Yes
vasdel.9.T:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasN.solo.Scer\UAS.P\T.T:Avic\GFP-YFP.Venus
0 Yes
vasQ525A.Scer\UAS.P\Tantimorphic allele - genetic evidence0 Yes
vasR551A.Scer\UAS.P\Tantimorphic allele - genetic evidence0 Yes
vasScer\UAS.P\T.cSa0 Yes
vassolo.T:Avic\GFP-YFP.Venus
0 Yes
vasT:Avic\GFP-EGFP0 Yes
vasT:Avic\GFP0 Yes
vasT:Disc\RFP-mCherry,T:Ivir\HA10 Yes
vasT:Ivir\HA1,T:Avic\GFP-EGFP0 Yes
vasT:Ivir\HA1,T:Ecol\lacZ0 Yes
vasαTub67C.T:Avic\GFP0 Yes
vasΔ-96-65.T:Ivir\HA1,T:Ecol\lacZ0 Yes
vasΔ30.T:Avic\GFP0 Yes
vasΔ616-618.T:Avic\GFP-EGFP0 Yes
vasΔ616.T:Avic\GFP-EGFP0 Yes
vasΔ617.T:Avic\GFP-EGFP0 Yes
vasΔ618.T:Avic\GFP-EGFP0 Yes
hide Aneuploid Aberrations
Disrupted in
Not disrupted in
Partially disrupted in
Duplicated in
hide Transgenic Constructs & Insertions
Transgenic Constructs
Type of construct
Name
Expression data
Insertions
Type of insertions
Name
Expression data
insertion of enhancer trap binary system
hide Gene Ontology: Function, Process & Cellular Component ( 29 unique terms )
hide Terms Based on Experimental Evidence ( 15 terms )
Molecular Function
CV term
References
inferred from direct assay
inferred from physical interaction with Dcr-1
inferred from physical interaction with Fmr1
inferred from physical interaction with gus
inferred from physical interaction with piwi
inferred from direct assay
Biological Process
CV term
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
Cellular Component
CV term
References
inferred from direct assay
inferred from direct assay
hide Terms Based on Predictions or Assertions ( 18 terms )
Molecular Function
CV term
References
Biological Process
CV term
References
traceable author statement
non-traceable author statement
traceable author statement
traceable author statement
non-traceable author statement
Cellular Component
CV term
References
traceable author statement
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Protein-protein
Interacting group
Assay
References
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Interacts with
Please look at the allele data for full details of the genetic interactions
vas allele
Gene
References
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Linkouts
DroID - A comprehensive database of gene and protein interactions.
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Genome-wide drosophilid orthologs
Curated drosophilid orthologs
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hide Stocks Listed in FlyBase ( 22 )
Bloomington
Harvard
Kyoto
VDRC
hide Genomic Clones ( 2 )
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
hide cDNA Clones ( 80 )
Please Note
This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see GBrowse for alignment of the cDNAs and ESTs to the gene model.
cDNA Clones, Fully Sequenced
BDGP DGC clones
Other clones
cDNA Clones, End Sequenced (ESTs)
BDGP DGC clones
Other clones
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Linkouts
DRSC - Results from RNAi screens.
GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
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monoclonal
polyclonal antibody
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Source for database identity of
Source for identity of: CG33678 BG:DS00929.15
Source for identity of: vas CG3506
Source for database merge of
Source for merge of: vas CG33678
Additional comments
Annotations CG3506 and CG33678 merged as CG43081 in release 5.31 of the genome annotation.
hide Other Comments
The "solo" splice variant encoded by the vas locus is required for meiotic cohesion.
vas binds with 1:1 stoichiometry to gus.
New annotation (CG33678) in release 4.2 of the genome annotation.
vas may act in the process of dorsal ventral polarity formation in the oocyte.
Mutants exhibit a ventralized egg chamber, the same phenotype that is observed in grk and Egfr mutants.
vas is involved in oocyte differentiation and germline cyst development.
vas is required, directly or indirectly, for the regulation of grk mRNA localisation.
vas is required for the establishment of both anterior-posterior and dorsal-ventral polarity of the oocyte.
The polarity defects of vas mutants appear to be caused by a reduction in the amount of grk protein at stages of oogenesis critical for the establishment of polarity.
An osk-vas complex seems to stimulates transcription of osk. The phosphorylation of short osk may act in the spatial restriction of osk translation to the posterior pole.
osk, stau, vas and tud are essential for pole plasm formation.
vas and tud are localised dependent of osk protein and are required to accumulate osk protein stably at the posterior pole.
Localization of vas protein to the nuage particles is independent of the pole plasm assembly pathway, but formation of the nuage depends upon vas function.
Molecular analysis of vas alleles suggests that recruitment of vas to the pole plasm must depend on protein-protein interactions, but, once localized, vas must bind to RNA to mediate germ cell formation.
Distribution of tud protein in mutant embryos has been studied.
The level of vas RNA in the ovary is controlled by the psq gene product.
Only vas and tud are essential for osk-induced pole cell and abdomen formation.
vas, vls and tud (but not stau, capu, or spir) are necessary for the 6xosk mutant phenotypes.
The vas gene is critical for normal and ectopic localization of the posterior signal.
BicD vas embryos suppress all abdominal development.
Mutations in vas do not interact with RpII140wimp.
Mutations at the vas locus cause defects in midoogenesis.
vas mutant embryos lack nos activity.
vas mutants exhibit deletion of the abdomen and pole plasm; amorphic mutants are sterile.
In vas mutants synthesis of vas protein is absent or severely restricted.
vas- females fail to complete oogenesis and lay no eggs.
vas plays a role in polar granule formation.
vas protein does not accumulate in embryos from females mutant for capu and spir.
Mutation in vas results in a maternal effect "grandchildless knirps-like" phenotype.
Mutations in vas cause failure of germ cell formation and deletions in the abdominal segments in the embryo.
hide External Crossreferences & Linkouts
Sequence Crossreferences
Entrez Gene - A searchable database of RefSeq genes.
Other Crossreferences
InterPro domains - A database of protein families, domains, and functional sites
Linkouts
DroID - A comprehensive database of gene and protein interactions.
DRSC - Results from RNAi screens.
FlyMine - Integrated genomics database for Drosophila, Anopheles, and C.elegans
GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
modMine - Data generated by the modENCODE project.
hide Synonyms & Secondary IDs ( 23 )
Reported As
Symbol Synonym
CG33678
 
fs(2)ltoRJ36
 
Name Synonym
female sterile(2)ltoRJ36
 
sisters on the loose
Vasa
(Parrott et al., 2011, Singh et al., 2010, Okegbe and DiNardo, 2011, Kugler et al., 2010, Leatherman and Dinardo, 2010, Deshpande et al., 2006, Terry et al., 2006, Siddall et al., 2006, Schupbach et al., 2006, O'Reilly et al., 2006, Klattenhoff et al., 2007, Sengoku et al., 2006, Poulton and Deng, 2006, Seydoux and Braun, 2006, Lin et al., 2006, Kugler and Lasko, 2007, Yamashita et al., 2007, Yamashita et al., 2007, Strome and Lehmann, 2007, Gilboa and Lehmann, 2006, Niki et al., 2006, Niki, 2006, Irion et al., 2006, Renault et al., 2004, Burnett and Howard, 2003, Clough et al., 2007, Maines et al., 2007, Renault et al., 2004, Song et al., 2007, Deshpande et al., 2007, Casper and Van Doren, 2006, Kadyrova et al., 2007, Yamada et al., 2008, Yamashita et al., 2005, Sano et al., 2005, Song et al., 2007, Sun et al., 2008, Neumuller et al., 2008, Wawersik et al., 2005, Yogev et al., 2008, Vanzo et al., 2007, Kitadate et al., 2007, Chicoine et al., 2007, Jiang et al., 2008, Orsborn et al., 2007, Bogard et al., 2007, Kunwar et al., 2008, Yang et al., 2007, Meignin and Davis, 2008, Chen et al., 2007, Tanentzapf et al., 2007, Chen et al., 2007, Suyama et al., 2009, Cheng et al., 2008, Ricardo and Lehmann, 2009, Clark et al., 2007, Bhat and Schedl, 1997, Yang et al., 2009, Aruna et al., 2009, Nanda et al., 2009, Gavis et al., 2008, Szakmary et al., 2009, Singh et al., 2006, Nie et al., 2009, Li et al., 2009, Bosveld et al., 2008, Chen et al., 2009, Liu et al., 2009, Gouw et al., 2009, Li et al., 2009, Sheng et al., 2009, Sheng et al., 2009, Guo and Wang, 2009, Klattenhoff et al., 2009, Hayashi et al., 2009, Riparbelli et al., 2009, Kalamegham et al., 2007, Bolivar et al., 2006, Riparbelli et al., 2005, Issigonis et al., 2009, Zhao et al., 2008, Adolph et al., 2009, Hashiyama et al., 2009, Jin et al., 2008, Leatherman and DiNardo, 2008, Patil and Kai, 2010, Liu et al., 2010, Grillo et al., 2011, Cheng et al., 2011, Gerbasi et al., 2011, Tastan et al., 2010, Kearse et al., 2011, Eliazer et al., 2011, König et al., 2011, Kugler et al., 2010, Sinsimer et al., 2011, McElwain et al., 2011, Monk et al., 2010, Zamparini et al., 2011)
Secondary FlyBase IDs
  • FBgn0003970
  • FBgn0004805
  • FBgn0028928
  • FBgn0053678
hide References ( 625 )
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hide Recent research papers ( 49 )
Casper et al., 2011, Development 138(16): 3357--3366
no child left behind encodes a novel chromatin factor required for germline stem cell maintenance in males but not females. [FBrf0214565]
Chan et al., 2011, Genetics 188(1): 33--44
Insect Population Control by Homing Endonuclease-Based Gene Drive: An Evaluation in Drosophila melanogaster. [FBrf0213627]
Cheng et al., 2011, Development 138(5): 831--837
Asymmetric division of cyst stem cells in Drosophila testis is ensured by anaphase spindle repositioning. [FBrf0213009]
Eliazer et al., 2011, Proc. Natl. Acad. Sci. U.S.A. 108(17): 7064--7069
Loss of lysine-specific demethylase 1 nonautonomously causes stem cell tumors in the Drosophila ovary. [FBrf0213593]
Gerbasi et al., 2011, Proc. Natl. Acad. Sci. U.S.A. 108(8): 3204--3209
Blanks, a nuclear siRNA/dsRNA-binding complex component, is required for Drosophila spermiogenesis. [FBrf0213185]
Grillo et al., 2011, Genetics 187(2): 513--521
Control of Germline torso Expression by the BTB/POZ Domain Protein Pipsqueak Is Required for Embryonic Terminal Patterning in Drosophila. [FBrf0213010]
Kearse et al., 2011, Nucleic Acids Res. 39(7): 2701--2716
Expression of ribosomal protein L22e family members in Drosophila melanogaster: rpL22-like is differentially expressed and alternatively spliced. [FBrf0213492]
Kibanov et al., 2011, Mol. Biol. Cell 22(18): 3410--3419
A novel organelle, the piNG-body, in the nuage of Drosophila male germ cells is associated with piRNA-mediated gene silencing. [FBrf0215572]
König et al., 2011, EMBO J. 30(8): 1549--1562
Ecdysteroids affect Drosophila ovarian stem cell niche formation and early germline differentiation. [FBrf0213531]
Lerit and Gavis, 2011, Curr. Biol. 21(6): 439--448
Transport of germ plasm on astral microtubules directs germ cell development in Drosophila. [FBrf0213255]
McElwain et al., 2011, PLoS ONE 6(11): e26993
A suppressor/enhancer screen in Drosophila reveals a role for wnt-mediated lipid metabolism in primordial germ cell migration. [FBrf0216663]
Okegbe and DiNardo, 2011, Development 138(7): 1259--1267
The endoderm specifies the mesodermal niche for the germline in Drosophila via Delta-Notch signaling. [FBrf0213233]
Parrott et al., 2011, PLoS ONE 6(9): e25087
Nucleoporin98-96 Function Is Required for Transit Amplification Divisions in the Germ Line of Drosophila melanogaster. [FBrf0216255]
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]
Richter et al., 2011, Nat. Cell Biol. 13(9): 1029--1039
The tumour suppressor L(3)mbt inhibits neuroepithelial proliferation and acts on insulator elements. [FBrf0215050]
Riparbelli and Callaini, 2011, Dev. Biol. 349(2): 427--439
Male gametogenesis without centrioles. [FBrf0212739]
Sinsimer et al., 2011, Development 138(16): 3431--3440
A late phase of germ plasm accumulation during Drosophila oogenesis requires Lost and Rumpelstiltskin. [FBrf0214542]
Sui and Yang, 2011, J. Genet. Genomics 38(2): 55--61
Distinct effects of nuclear membrane localization on gene transcription silencing in Drosophila S2 cells and germ cells. [FBrf0213132]
Tanaka et al., 2011, Development 138(12): 2523--2532
Drosophila Mon2 couples Oskar-induced endocytosis with actin remodeling for cortical anchorage of the germ plasm. [FBrf0213769]
Yadlapalli et al., 2011, J. Cell Sci. 124(6): 933--939
Drosophila male germline stem cells do not asymmetrically segregate chromosome strands. [FBrf0213200]
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]
Zhang et al., 2011, Mol. Cell 44(4): 572--584
Heterotypic piRNA Ping-Pong Requires Qin, a Protein with Both E3 Ligase and Tudor Domains. [FBrf0216809]
Zhou et al., 2011, Development 138(6): 1111--1120
Auxilin is required for formation of Golgi-derived clathrin-coated vesicles during Drosophila spermatogenesis. [FBrf0213068]
Anne, 2010, Development 137(17): 2819--2828
Arginine methylation of SmB is required for Drosophila germ cell development. [FBrf0211523]
Anne, 2010, PLoS ONE 5(12): e14362
Targeting and anchoring tudor in the pole plasm of the Drosophila oocyte. [FBrf0212588]
Bakhrat et al., 2010, Apoptosis 15(12): 1425--1434
Drosophila Chk2 and p53 proteins induce stage-specific cell death independently during oogenesis. [FBrf0212376]
Becalska and Gavis, 2010, Dev. Biol. 340(2): 528--538
Bazooka regulates microtubule organization and spatial restriction of germ plasm assembly in the Drosophila oocyte. [FBrf0210533]
Filippakopoulos et al., 2010, J. Mol. Biol. 401(3): 389--402
Structural Basis for Par-4 Recognition by the SPRY Domain- and SOCS Box-Containing Proteins SPSB1, SPSB2, and SPSB4. [FBrf0211386]
Gonsalvez et al., 2010, Development 137(14): 2341--2351
Sm proteins specify germ cell fate by facilitating oskar mRNA localization. [FBrf0211144]
Janic et al., 2010, Science 330(6012): 1824--1827
Ectopic expression of germline genes drives malignant brain tumor growth in Drosophila. [FBrf0212713]
Kirino et al., 2010, J. Biol. Chem. 285(11): 8148--8154
Arginine Methylation of Vasa Protein Is Conserved across Phyla. [FBrf0210172]
Kitadate and Kobayashi, 2010, Proc. Natl. Acad. Sci. U.S.A. 107(32): 14241--14246
Notch and Egfr signaling act antagonistically to regulate germ-line stem cell niche formation in Drosophila male embryonic gonads. [FBrf0211513]
Kugler et al., 2010, Mol. Cell. Biol. 30(7): 1769--1782
Regulation of Drosophila Vasa In Vivo through Paralogous Cullin-RING E3 Ligase Specificity Receptors. [FBrf0210170]
Kugler et al., 2010, PLoS ONE 5(2): e9048
Reduced cul-5 Activity Causes Aberrant Follicular Morphogenesis and Germ Cell Loss in Drosophila Oogenesis. [FBrf0209909]
Lancaster et al., 2010, PLoS Genet. 6(10): e1001179
The Meiotic Recombination Checkpoint Suppresses NHK-1 Kinase to Prevent Reorganisation of the Oocyte Nucleus in Drosophila. [FBrf0212208]
Leatherman and Dinardo, 2010, Nat. Cell Biol. 12(8): 806--811
Germline self-renewal requires cyst stem cells and stat regulates niche adhesion in Drosophila testes. [FBrf0211422]
Liu et al., 2010, Sci. Signal. 3(132): ra57
The Drosophila Female Germline Stem Cell Lineage Acts to Spatially Restrict DPP Function Within the Niche. [FBrf0211426]
Monk et al., 2010, Cell Stem Cell 6(4): 348--360
HOW is required for stem cell maintenance in the Drosophila testis and for the onset of transit-amplifying divisions. [FBrf0210446]
Nagao et al., 2010, RNA 16(12): 2503--2515
Biogenesis pathways of piRNAs loaded onto AGO3 in the Drosophila testis. [FBrf0212366]
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]
Patil and Kai, 2010, Curr. Biol. 20(8): 724--730
Repression of Retroelements in Drosophila Germline via piRNA Pathway by the Tudor Domain Protein Tejas. [FBrf0211166]
Quinones et al., 2010, J. Cell Biol. 189(2): 353--367
I-BAR protein antagonism of endocytosis mediates directional sensing during guided cell migration. [FBrf0210570]
Renault et al., 2010, Development 137(11): 1815--1823
Lipid phosphate phosphatase activity regulates dispersal and bilateral sorting of embryonic germ cells in Drosophila. [FBrf0210764]
Robinett et al., 2010, PLoS Biol. 8(5): e1000365
Sex and the single cell. II. There is a time and place for sex. [FBrf0210735]
Singh et al., 2010, J. Cell. Physiol. 223(2): 500--510
Competitiveness for the niche and mutual dependence of the germline and somatic stem cells in the Drosophila testis are regulated by the JAK/STAT signaling. [FBrf0210092]
Tastan et al., 2010, Development 137(19): 3167--3176
Drosophila Ataxin 2-binding protein 1 marks an intermediate step in the molecular differentiation of female germline cysts. [FBrf0211752]
Yan et al., 2010, J. Cell Biol. 188(3): 335--349
SOLO: a meiotic protein required for centromere cohesion, coorientation, and SMC1 localization in Drosophila melanogaster. [FBrf0209923]
Yu et al., 2010, genesis 48(3): 161--170
E(nos)/CG4699 required for nanos function in the female germ line of Drosophila. [FBrf0210233]
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Arkov and Ramos, 2010, Trends Cell Biol. 20(8): 482--490
Building RNA-protein granules: insight from the germline. [FBrf0212430]