A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\DoaHD

General Information
SymbolDmel\DoaHDSpeciesD. melanogaster
NameFlyBase IDFBal0002719
Feature typealleleAssociated geneDmel\Doa
Also Known AsDoaHD1, DoaHD2
Map ( GBrowse ) GBrowse View Helpdetailed view FBal0002719 FBal0033616 FBal0033615
Allele class
MutagenPM hybrid dysgenesistransposable element activity
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Description
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FB2013_03
Genes
Doa
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
sequence variant
linked_to=EcoRI-BamHI_rfrag
comment=mapped to restriction fragment in Figure 4 of FBrf0074875, position of restriction fragment on reference sequence inferred by FlyBase curator
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 copia{} element is inserted 177 nucleotides 3' to the first non-coding exon of Doa and 231 nucleotides 5' to the 55kD transcript's initiating AUG.
An uncharacterised 5kb transposable element in inserted within an intron.
Caused by insertion
Cytology
Polytene chromosomes normal.
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Statement
Reference
Doa[HD] heterozygous adults show significantly reduced sensitity to paraquat.
In Doa[HD]/Doa[s2784] mutants where the Doa[HD] allele is from the mother blackened areas are seen on the wings. When the Doa[s2784] allele comes from the mother the mutants die at or prior to the pupal stage. In Doa[HD]/Doa[5] mutants where the Doa[HD] allele is from the mother there is a strong transformation of females towards males, with male colouration of tergites 5 and 6, male sex combs on the prothoracic leg, and a normal but rotated female genital plate. When the Doa[5] allele comes from the mother there are no survivors.
Heterozygotes with Doa7 have ommatidia of varying size and disorganization of the interommatidial bristles. Random interruption of the normal lattice of pigment cells and random vacuolization of the retina and pigment cells are restored to at least normal levels (suppression of wa).
Crosses between DoaHD and Doa9 heterozygotes indicate that Doa is not an embryonic lethal, and is probably lethal during early larval stages. Rare DoaHD/Doa6 or DoaHD/Doa7 escapers of lethality are found at a frequency of approximately 0.5%. DoaHD/Doa6 escapers are more frequently female than male (ratio 4:1) and the male escapers are sterile despite having motile sperm.
Heterozygotes with Doa6 or Doa7 survive rarely and when they do, wa is darkened to nearly wild-type color; wsp55 reacts in the opposite manner, becoming nearly white; eyes of escapers have disarranged facets. Males of these heteroallelic combinations involving Doa6 are sterile despite having motile sperm; females and both sexes involving Doa7 are weakly fertile.
 
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Linkouts
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Statement
Reference
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hideNOT Enhanced by
Statement
Reference
Doa7/DoaHD has phenotype, non-enhanceable by gl2
Doa7/DoaHD has phenotype, non-enhanceable by gl60j
Doa7/DoaHD has phenotype, non-enhanceable by Ras85De2F
Doa7/DoaHD has phenotype, non-enhanceable by rl1
Doa7/DoaHD has phenotype, non-enhanceable by rlSem
Doa7/DoaHD has phenotype, non-enhanceable by sina1
DoaHD/DoaDem has phenotype, non-enhanceable by EgfrE1
DoaHD/DoaDem has phenotype, non-enhanceable by gl2
DoaHD/DoaDem has phenotype, non-enhanceable by gl60j
DoaHD/DoaDem has phenotype, non-enhanceable by Ras85De2F
DoaHD/DoaDem has phenotype, non-enhanceable by rl1
DoaHD/DoaDem has phenotype, non-enhanceable by rlSem
DoaHD/DoaDem has phenotype, non-enhanceable by sina1
hideNOT suppressed by
Statement
Reference
Doa7/DoaHD has phenotype, non-suppressible by gl2
Doa7/DoaHD has phenotype, non-suppressible by gl60j
Doa7/DoaHD has phenotype, non-suppressible by Ras85De2F
Doa7/DoaHD has phenotype, non-suppressible by rl1
Doa7/DoaHD has phenotype, non-suppressible by rlSem
Doa7/DoaHD has phenotype, non-suppressible by sina1
DoaHD/DoaDem has phenotype, non-suppressible by EgfrE1
DoaHD/DoaDem has phenotype, non-suppressible by gl2
DoaHD/DoaDem has phenotype, non-suppressible by gl60j
DoaHD/DoaDem has phenotype, non-suppressible by Ras85De2F
DoaHD/DoaDem has phenotype, non-suppressible by rl1
DoaHD/DoaDem has phenotype, non-suppressible by rlSem
DoaHD/DoaDem has phenotype, non-suppressible by sina1
hideEnhancer of
Statement
Reference
DoaHD is an enhancer of phenotype of wsp55
hideNOT Enhancer of
Statement
Reference
DoaHD is a non-enhancer of phenotype of wa2
DoaHD is a non-enhancer of phenotype of wa3
DoaHD is a non-enhancer of phenotype of wa4
DoaHD is a non-enhancer of phenotype of wa57i11
DoaHD is a non-enhancer of phenotype of wa58l
DoaHD is a non-enhancer of phenotype of wa59k1
DoaHD is a non-enhancer of phenotype of wapl
DoaHD is a non-enhancer of phenotype of wbf2
DoaHD is a non-enhancer of phenotype of wbf
DoaHD is a non-enhancer of phenotype of wbl
DoaHD is a non-enhancer of phenotype of wBwx
DoaHD is a non-enhancer of phenotype of wco
DoaHD is a non-enhancer of phenotype of wcol
DoaHD is a non-enhancer of phenotype of we2
DoaHD is a non-enhancer of phenotype of wE
DoaHD is a non-enhancer of phenotype of we
DoaHD is a non-enhancer of phenotype of wec3
DoaHD is a non-enhancer of phenotype of wh
DoaHD is a non-enhancer of phenotype of wi
DoaHD is a non-enhancer of phenotype of wIR1
DoaHD is a non-enhancer of phenotype of wIR2
DoaHD is a non-enhancer of phenotype of wIR3
DoaHD is a non-enhancer of phenotype of wIR4
DoaHD is a non-enhancer of phenotype of wIR5
DoaHD is a non-enhancer of phenotype of wIR6
DoaHD is a non-enhancer of phenotype of wmo
DoaHD is a non-enhancer of phenotype of wr
DoaHD is a non-enhancer of phenotype of wsat
DoaHD is a non-enhancer of phenotype of wsp2
DoaHD is a non-enhancer of phenotype of wsp81d
DoaHD is a non-enhancer of phenotype of wzm
DoaHD is a non-enhancer of phenotype of y2
hideSuppressor of
Statement
Reference
DoaHD is a suppressor of phenotype of wa
DoaHD is a suppressor of phenotype of waM
DoaHD is a suppressor of phenotype of waR84h
hideNOT Suppressor of
Statement
Reference
DoaHD is a non-suppressor of phenotype of wa2
DoaHD is a non-suppressor of phenotype of wa3
DoaHD is a non-suppressor of phenotype of wa4
DoaHD is a non-suppressor of phenotype of wa57i11
DoaHD is a non-suppressor of phenotype of wa58l
DoaHD is a non-suppressor of phenotype of wa59k1
DoaHD is a non-suppressor of phenotype of wapl
DoaHD is a non-suppressor of phenotype of wbf2
DoaHD is a non-suppressor of phenotype of wbf
DoaHD is a non-suppressor of phenotype of wbl
DoaHD is a non-suppressor of phenotype of wBwx
DoaHD is a non-suppressor of phenotype of wco
DoaHD is a non-suppressor of phenotype of wcol
DoaHD is a non-suppressor of phenotype of we2
DoaHD is a non-suppressor of phenotype of wE
DoaHD is a non-suppressor of phenotype of we
DoaHD is a non-suppressor of phenotype of wec3
DoaHD is a non-suppressor of phenotype of wh
DoaHD is a non-suppressor of phenotype of wi
DoaHD is a non-suppressor of phenotype of wIR1
DoaHD is a non-suppressor of phenotype of wIR2
DoaHD is a non-suppressor of phenotype of wIR3
DoaHD is a non-suppressor of phenotype of wIR4
DoaHD is a non-suppressor of phenotype of wIR5
DoaHD is a non-suppressor of phenotype of wIR6
DoaHD is a non-suppressor of phenotype of wmo
DoaHD is a non-suppressor of phenotype of wr
DoaHD is a non-suppressor of phenotype of wsat
DoaHD is a non-suppressor of phenotype of wsp2
DoaHD is a non-suppressor of phenotype of wsp81d
DoaHD is a non-suppressor of phenotype of wzm
DoaHD is a non-suppressor of phenotype of y2
hideOther
Statement
Reference
hide Additional Comments
hide Genetic Interactions
Statement
Reference
Doa[HD] Ef1γ[GE29510]/Doa[Dem] flies show a number of defects, including ectopic wing venation, failure of either of the crossveins to attach (particularly the posterior crossvein in males), aberrantly formed crossveins, occasional eye roughness, curved wings and rarely, partial rotation of the female genitalia.
DoaHD in combination with E(gl)3Cunspecified results in flies with normal eyes, wings and bristles. No suppression of wa is seen in these flies.
Rare DoaHD/Doa6 or DoaHD/Doa7 escapers show extreme suppression of the wa phenotype, such that eyes, Malpighian tubules, ocelli and testes are essentially wild-type in colour. They have disordered eye facets and scutellar bristles are often missing or abnormal. Male escapers carrying wsp55 have bleach-white eyes.
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Statement
Reference
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Comments
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hide Notes on Origin
Discoverer
The "HD1" and "HD2" alleles have an insertion in an identical location. They both potentially originate from a single event during mass crosses.
hide Comments
Does not interact with gypsy induced alleles at several loci (f1, y2 and ct6).
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Other Crossreferences
Linkouts
hide Synonyms & Secondary IDs ( 5 )
Reported As
Symbol Synonym
Doa1
 
Doa2
 
Name Synonym
Secondary FlyBase IDs
  • FBal0002720
hide References ( 10 )
Research paper
Fan et al., 2010, Genetics 184(1): 141--154
Drosophila translational elongation factor-1{gamma} is modified in response to DOA kinase activity and is essential for cellular viability. [FBrf0209673]
James et al., 2009, Free Radical Biol. Med. 46(6): 821--827
Superoxide dismutase is regulated by LAMMER kinase in Drosophila and human cells. [FBrf0207123]
Kpebe and Rabinow, 2008, Genetics 179(4): 1973--1987
Dissection of darkener of apricot kinase isoform functions in Drosophila. [FBrf0205853]
Morris et al., 2003, Genetics 164(4): 1435--1446
Identification and analysis of mutations in bob, Doa and eight new genes required for oocyte specification and development in Drosophila melanogaster. [FBrf0162144]
Yun et al., 2000, Genetics 156(2): 749--761
The LAMMER protein kinase encoded by the Doa locus of Drosophila is required in both somatic and germline cells and is expressed as both nuclear and cytoplasmic isoforms throughout development. [FBrf0130184]
Yun et al., 1994, Genes Dev. 8(10): 1160--1173
The Doa locus encodes a member of a new protein kinase family and is essential for eye and embryonic development in Drosophila melanogaster. [FBrf0074875]
Rabinow et al., 1993, Genetics 134(4): 1175--1185
Mutations at the darkener of apricot locus modulate transcript levels of copia and copia-induced mutations in Drosophila melanogaster. [FBrf0058584]
Rabinow and Birchler, 1990, Genet. Res. (Camb.) 55: 141--151
Interactions among modifiers of retrotransposon-induced alleles of the white locus of Drosophila melanogaster. [FBrf0051869]
Rabinow and Birchler, 1989, EMBO J. 8: 879--889
A dosage-sensitive modifier of retrotransposon-induced alleles of the Drosophila white locus. [FBrf0049635]
Abstract
Staatz et al., 2005, A. Dros. Res. Conf. 46: 373A
Doa regulates TrxR-1481 and Sod-2. [FBrf0183505]