A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\wDZL

General Information
SymbolDmel\wDZLSpeciesD. melanogaster
NameDominant zeste-likeFlyBase IDFBal0018236
Feature typealleleAssociated geneDmel\w
Map ( GBrowse ) Untitled Document detailed view FBti0036648 FBti0034753 FBti0132267 FBti0029995 FBti0016461 FBti0069870 FBti0001367 FBti0010587 FBti0014801 FBti0002409 FBti0042629 FBti0066148 FBti0002389 FBti0029317 FBti0043908 FBti0001368 FBti0036262 FBti0002388 FBti0035372 FBti0014803 FBti0014807 FBti0034094 FBti0050142 FBti0036739 FBti0014762 FBti0036414 FBti0055730 FBti0066756 FBti0067472 FBti0002390 FBti0002387
Allele class
Mutagenspontaneous
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Description
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FB2013_03
FB2013_02
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hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
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 of FB sequences into the upstream regulatory region of w.
Caused by a foldback element upstream of the normal regulatory sequences of w.
Insertion of FB element.
Insertion of a composite transposon 5-6kb 5' to w, resulting in a novel transcription unit that is expressed in the head. The transposon consists of a 6.5kb portion, originating at cytological locus 21D, flanked by two FB transposons.
Insertion of a 13 kb FB-element at map position +9.8 relative to the transcription start site of w.
FB insertion between coordinates +9.5 and +10, using coordinate system of FBrf0038648 where coordinate 0 is the copia insert of wa.
Physical analysis of wDZL shows that the mutant phenotype results from the insertion (proximal to white) of a complex transposable element made up of sequences normally found at 21D ('unique segment sequences') flanked by sequences of two FB transposons (Levis et al., 1982; Zachar and Bingham, 1982; Bingham and Zachar, 1985). A transcript 1.3 kb larger than the major (2.6 kb) w+ transcript is found in wDZL adult heads and head precursor tissues; this is a composite transcript, made up of sequences from the major w+ transcript and from the wDZL unique segment (Bingham and Zachar, 1985; Zachar, Chapman and Bingham, 1985). In wDZL flies, a reduction in the levels of the w+ transcript is observed in adult head and head precursor tissues, but not in abdominal tissues. Revertants of wDZL show loss of most of the unique segments of the insertion with 1.9 and 6.2 kb of the insertion remaining (Levis and Rubin, 1982; Zachar and Bingham, 1982). 13kb FB insertion map site (kb): +9.77; Origin = insertion of wa copia; '-' values to left (telomere) end; '+' values to right (centromere) end.
 
Caused by insertion
Caused by aberration
Cytology
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Statement
Reference
Eye colour: z-like. Shows some interaction with Inr-a mutants.
Eye colour: dull red brown, in z+ males. Eye colour: yellow, in heterozygous or homozygous females. Eye colour: wild-type in In(1)wDZL-1/wDZL, T(1;3)wDZL/wDZL females. Eye colour: wild-type in In(1)wDZL-3/wDZL females.
Eye colour: dull red brown, in z+ males. Eye colour: yellow, in z1 males and in homo- and heterozygous females (z+ or z1) when X's synapsed. Malpighian tubule colour: wild-type. Testis colour: wild-type.
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Statement
Reference
wDZL has eye color defective phenotype, enhanceable by Low1
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hideEnhanced by
Statement
Reference
wDZL has phenotype, enhanceable by Wowems1
wDZL has phenotype, enhanceable by Wowhd1
wDZL has phenotype, enhanceable by Wowγb
wDZL has phenotype, enhanceable by Wowγe
wDZL has pigment cell phenotype, enhanceable by Low1
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hide Genetic Interactions
Statement
Reference
Female progeny of w+ crossed to wDZL, Wow- have reduced eye pigment. When z1 wDZL are crossed to Wow mutants, Wow has no effect on the eye color of sons.
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Statement
Reference
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Comments
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Bloomington
3603
Kyoto
hide Notes on Origin
Discoverer
Bingham.
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Unstable mutation that creates revertants that carry internal deletion of the FB element.
Located in or immediately proximal to the rightmost set of previously-defined w mutant sites Mutable allele; spontaneous mutations are observed at a frequency of 0.5 to 1.5%.
wDZL shows synapsis-dependent dominance over w+. It is a highly mutable allele (like wc), giving rise spontaneously to w+ and w- derivatives with a frequency of 0.5-1.5%.
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hide Synonyms & Secondary IDs ( 2 )
Reported As
Symbol Synonym
wDZL
 
Name Synonym
Dominant zeste-like
 
Secondary FlyBase IDs
hide References ( 18 )
Research paper
Bhadra et al., 1997, Genetics 146(3): 903--917
A sex-influenced modifier in Drosophila that affects a broad spectrum of target loci including the histone repeats. [FBrf0094158]
Birchler et al., 1994, Genetics 137(4): 1057--1070
Weakener of white (Wow), a gene that modifies the expression of the white eye color locus and that suppresses position effect variegation in Drosophila melanogaster. [FBrf0074960]
Rabinow et al., 1991, Genetics 129: 463--480
A trans-acting regulatory gene that inversely affects the expression of the white, brown and scarlet loci in Drosophila. [FBrf0054158]
Harden and Ashburner, 1990, Genetics 126: 387--400
Characterization of the FB-NOF transposable element of Drosophila melanogaster. [FBrf0051943]
Bingham and Zachar, 1985, Cell 40: 819--825
Evidence that two mutations, wDZL and z1, affecting synapsis-dependent genetic behavior of white are transcriptional regulatory mutations. [FBrf0042055]
Ryo et al., 1985, Genetics 110: 441--451
Comparison of somatic reversions between the ivory allele and transposon-caused mutant alleles at the white locus of Drosophila melanogaster after larval treatment with X rays and ethyl methanesulfonate. [FBrf0042640]
Zachar et al., 1985, Cold Spring Harbor Symp. Quant. Biol. 50: 337--346
On the molecular basis of transvection effects and the regulation of transcription. [FBrf0042164]
Gehring et al., 1984, EMBO J. 3: 2077--2085
Functional analysis of the white+ gene of Drosophila by P-factor-mediated transformation. [FBrf0040771]
Hazelrigg et al., 1984, Cell 36: 469--481
Transformation of white locus DNA in Drosophila: Dosage compensation, zeste interaction, and position effects. [FBrf0040489]
O'Hare et al., 1984, J. Mol. Biol. 180: 437--455
DNA sequence of the white locus of Drosophila melanogaster. [FBrf0041384]
Collins et al., 1983, Yb. Carnegie Instn, Wash. 82: 180--182
Transposable genetic elements and the white locus of Drosophila. [FBrf0063381]
McGinnis and Beckendorf, 1983, Nucleic Acids Res. 11: 737--751
Association of a Drosophila transposable element of the roo family with chromosomal deletion breakpoints. [FBrf0040067]
Levis and Rubin, 1982, Cell 30: 543--550
The unstable wDZL mutation of Drosophila is caused by a 13 kilobase insertion that is imprecisely excised in phenotypic revertants. [FBrf0037613]
Levis et al., 1982, Cell 30: 551--565
FB elements are the common basis for the instability of the wDZL and wc Drosophila mutations. [FBrf0037614]
Levis et al., 1982, Proc. Natl. Acad. Sci. U.S.A. 79(2): 564--568
Physical map of the white locus of Drosophila melanogaster. [FBrf0038648]
Zachar and Bingham, 1982, Cell 30: 529--541
Regulation of white locus expression: The structure of mutant alleles at the white locus of Drosophila melanogaster. [FBrf0037612]
Bingham, 1981, Cold Spring Harbor Symp. Quant. Biol. 45(2): 519--525
A novel dominant mutant allele at the white locus of Drosophila melanogaster is mutable. [FBrf0036017]
Bingham, 1980, Genetics 95(2): 341--353
The regulation of white locus expression: A dominant mutant allele at the white locus of Drosophila melanogaster. [FBrf0034850]