FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\trxE3
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General Information
Symbol
Dmel\trxE3
Species
D. melanogaster
Name
FlyBase ID
FBal0017175
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

trxE3 is associated with an in-frame deletion that removes 271 amino acids from both TRXI and TRXII isoforms. The deleted residues are located on the C-terminal side of the central cysteine-rich domain that contains PHD fingers.

Deletion of a 280 amino acid domain, domain E3.

700bp deletion within coding region.

Deletion of 832bp DNA and insertion of 19 nucleotides, resulting in a deletion of 271 amino acids.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

Deletion of 832 nucleotides and insertion of 19 nucleotides leads to an in frame deletion of 271 amino acids.

Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

The brains of trxE3/trxB11 larvae show a severe reduction in BrdU incorporation compared to wild type. Brain squashes are characterised by global chromatin decondensation, resembling 'prophase-like' chromatin.

1.6% of heterozygous adults show at least one transformation phenotype. Hemizygotes are recessive lethal dying at the pupal stage, homozygotes are embryonic lethal. trxE3/Df(3R)red-P52 hemizygotes show phenotypes that suggest decreased Scr function (transformation of T1 structures to a T2 identity), decreased Ubx function (transformation of T3 to T2), decreased abd-A function (transformation of A2-A7 to A1) and decreased Abd-B function (transformation of posterior abdominal segments to more anterior abdominal identities). Scr group transformations include the development of mesothoracic tibial preapical bristles or mesothoracic tibial apical bristles on the prothoracic tibia, reduced numbers of sex comb teeth (in males), development of sternopleural bristles on the T1 segment. Ubx group transformations include haltere to wing, metathoracic laterotergite to scutum, the development of T3 sternopleural bristles, mesothoracic tibial preapical bristles or mesothoracic tibial apical bristles on the metathoracic tibia. abd-A group transformations include, the development of A1 type bristles on abdominal tergites 2 to 3 Abd-B group transformations include, the pigmentation of abdominal tergites 5 to 6 in males, and enlargement of abdominal tergite 7. Flies transheterozygous for trxE3 and a strong trx hypomorph, especially, trxZ16, frequently have missing dorsal head structures, including different combinations of ocelli, ocellar bristles, and postvertical bristles. The posterior border of the A1 tergite may have Uab-like bristles and dark pigmentation. They can also exhibit incomplete dorsal fusion of tergites. The dorsal anal plate of females may be incomplete. Many trxE3 hemizygotes develop as incomplete pharate adults whose heads fail to evert (and appear headless). They also have incomplete chitinisation.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Statement
Reference

trxE3/trx[+] is a suppressor of visible | homeotic phenotype of AntpNs, Pc2

Phenotype Manifest In
Suppressor of
Statement
Reference

trxE3/trx[+] is a suppressor of antenna phenotype of AntpNs, Pc2

trxE3/trx[+] is a suppressor of sex comb phenotype of AntpScx, Pc2

Additional Comments
Genetic Interactions
Statement
Reference

Suppresses the antenna to leg transformation phenotype of Pc2, AntpNs/+. Causes between 50% and 100% suppression of the Pc4/+ extra sex combs phenotype.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Partial complementation between hypomorphs produced phenotypes that were weaker than either of the hemizygous or homozygous phenotypes, either rescuing lethality or producing a weaker homeotic transformation phenotype. Transformations range from an average of 0.12 to 7.90 transformations/fly (males were scored for a possible 29 transformations, females were scored for a possible 26 transformations) in different allelic combinations.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

The following alleles form a series of progressively increasing penetrance and expressivity of phenotype when in transheterozygous combination with trx1 : trxM17 > trxZ32 > trxZ16 > trxZ11 > trxM18 = trxJY16 > trxE3.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (8)