A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Gene Dmel\Ste

General Information
SymbolDmel\SteSpeciesD. melanogaster
NameStellateAnnotation symbol
Feature typeprotein_coding_geneFlyBase IDFBgn0003523
Gene Model StatusNot Applicable Stock availability 5 publicly available
Genomic Location
Chromosome (arm)Recombination map1-45.7
Cytogenetic map12E1-12E2Sequence location
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Automatically generated summary

See sections below for more information
The gene Stellate is referred to in FlyBase by the symbol Dmel\Ste (FBgn0003523). This gene record represents a gene family, individual members of the family are: CG33236, CG33237, CG33238, CG33239, CG33240, CG33241, CG33242, CG33243, CG33244, CG33245, CG33246, CG33247. Based on sequence similarity, it is predicted to have molecular function: protein kinase regulator activity. There is experimental evidence that it is involved in the biological process: spermatogenesis. 12 alleles are reported. The phenotype of these alleles is annotated with: spermatocyte. It has no annotated transcripts. Protein features are: Casein kinase II, regulatory subunit; Casein kinase II, regulatory subunit, alpha-helical; Casein kinase II, regulatory subunit, beta-sheet. Gene has not been localized to the genome sequence.

hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
Ste: Stellate
This locus is responsible for the appearance of crystals in the nuclei and cytoplasm of primary spermatocytes of XO males. Enzymatic treatments indicate that these crystals are proteinaceous in nature (Meyer et al.). The suppression of crystal formation by the Y chromosome is attributable to a sequence designated Su(Ste).
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Description
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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
12E1-12E2  
Left limit from inclusion within Df(1)R12.1 (FBrf0079138) Right limit from in situ hybridisation (FBrf0079138)  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
12E1-12E2  
(determined by in situ hybridisation)  
12D1-12F2  
(determined by in situ hybridisation)  
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
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Comments on Gene Model
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Annotated Transcripts
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FlyBase ID
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Annotated Polypeptides
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FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
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InterPro domains - A database of protein families, domains, and functional sites
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DDBJ /
EMBL /
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DNA sequence
Protein sequence
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Lethality
Allele
Sterility
Allele
Phenotype manifest in
Allele
hide Classical Alleles ( 5 )
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Allele of SteClassMutagenStocksKnown lesion
Ste1
3 --
Stef08020c
1 --
SteR301.21 Yes
Steunspecified
0 --
SteW120 Yes
hide Alleles Carried on Transgenic Constructs ( 7 )
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Allele of SteClassMutagenStocksKnown lesion
Ste134.T:Ecol\lacZ0 Yes
Ste225.T:Ecol\lacZ0 Yes
SteALS.T:Scer\ilv20 Yes
StedsRNA.cAa0 Yes
Stehs.T:Ecol\lacZ0 Yes
Stemut.134.T:Ecol\lacZ0 Yes
SteβTub85D.T:Ecol\lacZ0 Yes
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Duplicated in
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Transgenic Constructs
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characterization construct
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Type of insertions
Name
Expression data
miscellaneous insertions
hide Gene Ontology: Function, Process & Cellular Component ( 5 unique terms )
hide Terms Based on Experimental Evidence ( 3 terms )
Molecular Function ( 0 terms)
Biological Process
CV term
References
inferred from genetic interaction with Su(Ste)
Cellular Component
CV term
References
inferred from direct assay
inferred from direct assay
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Molecular Function
CV term
References
inferred from electronic annotation with InterPro:IPR000704, InterPro:IPR016149, InterPro:IPR016150
inferred from sequence or structural similarity
non-traceable author statement
Biological Process
CV term
References
non-traceable author statement
traceable author statement
Cellular Component
CV term
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Interacts with
Please look at the allele data for full details of the genetic interactions
Ste allele
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Bloomington
Harvard
Kyoto
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Source for database identity of
Source for database merge of
Source for merge of: Ste BcDNA:GM31840
Component gene(s)
Additional comments
Annotation CG32605 split into 12 annotations, each representing a member of the Ste cluster, in release 3.2 of the genome annotation. The 12 annotations are: Ste:CG33236, Ste:CG33237, Ste:CG33238, Ste:CG33239, Ste:CG33240, Ste:CG33241, Ste:CG33242, Ste:CG33243, Ste:CG33244, Ste:CG33245, Ste:CG33246 and Ste:CG33247.
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Extrachromosomal circular DNA (eccDNA) is present throughout the fly's life cycle. The eccDNA population contains circular multimers of tandemly repeated genes, including Ste.
"Stellate-like" sequences (Ste, Su(Ste), SteXh and Ste12DOR) contain a common region of sequence, defined as the "Stellate-specific central core". Specific regions at either the 5' or 3' end of this core sequence distinguish different Stellate-like sequences from each other. Euchromatic Ste sequences all contain at their 5' end a region corresponding to the 3' end of the ben gene.
Ste-/Su(Ste)- males have exactly the same meiotic drive phenotype as Ste+/Su(Ste)- males.
The high extent of homology between Ste and Su(Ste) repeats suggested a possibility of Ste suppression by antisense transcription of Su(Ste) elements: however the detection of only "sense" Su(Ste) cDNAs in testis cDNA library argues against this proposal.
One of a class of genes with TATA-less promoters that have a subset of the conserved DPE sequence.
The relationship of Ste copy number and organisation to meiotic behaviour in Su(Ste)- males has been examined genetically and cytologically. Heterochromatic and euchromatic Ste repeats are functional, the abnormalities in chromosome condensation and frequency of nondisjunction is related to the Ste copy number. Meiosis is disrupted after synapsis and Su(Ste) induced meiotic drive is probably not mediated by Ste.
The Ste locus contains two major size classes of a tandemly repeated gene. Analysis using segmental Y deficiencies shows that Su(Ste) represses both the high levels and efficient splicing of Ste RNA.
"1-45.7" was stated as revision.
This locus is responsible for the appearance of crystals in the nuclei and cytoplasm of primary spermatocytes of X0 males. Enzymatic treatments indicate that these crystals are proteinaceous in nature (Meyer, Hess and Beermann, 1961). The suppression of crystal formation by the Y chromosome is attributable to a sequence designated Su(Ste).
 
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Sequence Crossreferences
Other Crossreferences
InterPro domains - A database of protein families, domains, and functional sites
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DroID - A comprehensive database of gene and protein interactions.
FLIGHT - Cell culture data for RNAi and other high-throughput technologies
hide Synonyms & Secondary IDs ( 11 )
Reported As
Symbol Synonym
BcDNA:GM31840
 
Name Synonym
euchromatic Ste
euchromatic Stellate
Secondary FlyBase IDs
  • FBgn0063181
hide References ( 125 )
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hide Recent research papers ( 5 )
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]
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]
Nagao et al., 2010, RNA 16(12): 2503--2515
Biogenesis pathways of piRNAs loaded onto AGO3 in the Drosophila testis. [FBrf0212366]
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]
Specchia et al., 2010, Nature 463(7281): 662--665
Hsp90 prevents phenotypic variation by suppressing the mutagenic activity of transposons. [FBrf0209921]
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