A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(2R)trix

General Information
SymbolDmel\Df(2R)trixSpeciesD. melanogaster
NameDeficiency (2R) transformer intersexFlyBase IDFBab0002231
Feature typechromosomal_deletion
Also Known AsDfTRIX, Df(2)TRIX
Computed Breakpoints include 51A2;51B6
Deleted segment51A2--51B6
Sequence coordinates
Member of large scale dataset(s)
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Description
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FB2013_03
FB2013_02
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hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data l(2)s3475 << bk1 << auk << bk2 << Sec61β
Genetic mapping information
Comments
Breakpoint(s) molecularly mapped
hide Comments on Cytology
Ref: Lindsley and Zimm, 1992
Left limit of break 1 from polytene analysis (FBrf0076124) Right limit of break 1 from inclusion of l(2)03563 (FBrf0067338) Limits of break 2 from polytene analysis (FBrf0049325)
 
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
hide Gene Deletion & Duplication Data
hide Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Molecular Data
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Complementation Data
Molecular Data
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Complementation Data
Molecular Data
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Complementation Data
Molecular Data
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In combination with other aberrations
NOT in combination with other aberrations
Df(2R)trix embryos from heterozygous mothers show segregation defects in anaphase and telophase as judged by the presence of chromatin bridges. These embryos show a higher level of "nuclear fallout", a process that removes nuclei with abnormal mitoses, than wild-type embryos. Fallout nuclei tend to be observed in pairs or clusters. There is no evidence of metaphase defects in these embryos and have a late telophase appearance.
Heterozygosity for Df(2R)trix results in 2.2% X chromosome nondisjunction and 1.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Enhances the trx-G homeotic transformations of Df(3R)red1. Strongly enhances both the extra sex comb and abdominal segment transformation phenotypes of Pc4.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Hemizygosity strongly suppresses the phl::tor12D.hs.sev phenotype.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Suppressor of the dosage dependent (two or more copies of P{sev-svp1} or P{sev-svp2}) transformation of cone cells into R7 photoreceptors and at a lower frequency R7 cells into outer photoreceptors.
Deficient embryos show a mutant midgut phenotype: central and posterior constrictions absent.
Mutation does not affect the level of w expression in ph-plac+3 flies.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Homozygous trix larvae show abdominal setal-belt phenotype in thorax.
 
hide Stocks ( 3 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
B.S. Baker.
 
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The Df(2R)trix chromosome acts as a dominant weak suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion), but this is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by one or more nonsuppressing deficiencies.
hide Synonyms & Secondary IDs ( 8 )
Reported As
Symbol Synonym
Name Synonym
Deficiency (2R) transformer intersex
 
Secondary FlyBase IDs
hide References ( 81 )
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hide Recent research papers ( 1 )
Sarno et al., 2011, Int. J. Dev. Biol. 55(10-11-12): 975--979
Effect of the transformer-2 gene of Anastrepha on the somatic sexual development of Drosophila. [FBrf0217213]