FB2024_03 , released June 25, 2024
Allele: Dmel\trc1
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General Information
Symbol
Dmel\trc1
Species
D. melanogaster
Name
FlyBase ID
FBal0017031
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: R395P.

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

G19832341C

Amino acid change:

R391P | trc-PA; R395P | trc-PB

Reported amino acid change:

R395P

Comment:

Position of mutation on reference sequence inferred by FlyBase curator. Difference in amino acid position due to slightly different predicted cds used by authors.

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

trc1/Df(3L)BSC445 mutant third instar larvae show a significant increase in the proportion of dorsal midline ddaC dendrite length that is enclosed within the epidermis rather than attached to the ECM. The amount of enclosed dendrite seen in each heterozygote is similar to wild type. Most of the dendritic crossings in these mutants are between enclosed dendrites and dendrites attached to the ECM and are thus non-contacting.

Females carrying homozygous follicle cell clones can produce round eggs.

trc1/+ heterozygotes exhibit wild-type dendritic tiling, with wild-type levels of dendritic crossing points per υm[2].

trc1 mutants exhibit supernumerary terminal branching and defective dendritic tiling. Mutant larvae show an increase in terminal branch number, and the branches of ddaC neurons often overlap each other. This tiling defect can be seen independently from the overbranching defect. The crossing branches have rigid and straight trajectories. When somatic clones are made in the neurons, mutant ddaE, IdaA and ddaC dendrites display a 50% increase in the number of branches. Mutant clones also exhibit a tiling defect. In mutants, the v'ada and vdaB dendrites often invade neighbouring fields. Major branches as well as terminal branches overlap extensively.

trc1/trc8 mutant show a variable delay in developmental rate.

trc1/trc8 mutant pupae can have multiply split laterals on the aristae. Laterals are seen to split at a wide range of developmental stages. As development proceeds, the distance from the proximal base of the lateral to the proximal most branch-point increases, as does the distance between the proximal and distal branch-points. An increase in the length of the arms distal to branch-points is also seen.

trc1/trc8 clones in the wing produce a weak multiple hair cell phenotype. Some hairs are split distally. The hairs appear clustered close together. In some cases the hairs are oriented almost orthogonally to the plane of the wing. trc1/Df(3L)kto2 larvae have an abnormal pattern of denticles, with the wild-type fairly precise rows of denticles being replaced by a more chaotic arrangement. At the level of the individual denticle, the predominant abnormality is splitting (more than 30% of denticles in some denticle bands show this phenotype). trc1/trc8 flies routinely show branching of one or more of the lateral extensions of the antenna.

Mutant wing and notum have rosettes of three or more short trichomes instead of single long hairs as in wild type. Useful as cell marker. Mutant cell autonomous in mitotic cells in a wild-type background, but not in a Minute background (Vinson and Adler, 1987, D. I. S. 66).

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhancer of
Statement
Reference

trc1 is an enhancer of wing hair phenotype of ultA1

Other
Statement
Reference

fry2/fry[+], matse235, trc1/trc[+] has wing hair | increased number phenotype

Additional Comments
Genetic Interactions
Statement
Reference

The level of non-contacting dendrite crossing in class IV dendrite arborizing larval neurons is significantly increased in trc1;Df(2R)Sema-2b-C4 double mutants compared to either trc1/+ or Df(2R)Sema-2b-C4/+ heterozygotes.

trc1/Mob2H4-5 double heterozygous third instar larvae show a neuromuscular junction (NMJ) overgrowth phenotype comparable to that seen in Mob2H4-5 single homozygotes: both bouton number and branch points per NMJ are increased compared to wild type.

stanE59/trc1 double heterozygous larvae show increased crossing of dendrites in the dendritic arbor of the ddaC class IV neurons compared to wild type (neither single heterozygote shows this phenotype).

Class IV da neurons of Sin1e03756/+ ; trc1/+, rictorΔ2/+ ; trc1/+ and TorΔP/+ ; trc1/+ double heterozygous larvae show defects in dendritic tiling, with a significantly higher number of dendritic branches crossing one another compared to wild type.

trc1/+ tutl23/+ double heterozygotes do not show any enhanced class I da neuron branching defects or class IV neuron dendrite self-avoidance defects compared to tutl23/+ single heterozygotes.

Transheterozygotes for trc1/hpoMGH4 exhibit obvious iso-neuronal as well as hetero-neuronal tiling defects, including a significant increase in dendritic crossing-points compared to single mutants.

Transheterozygotes for wtsx1/trc1 do not show any significant dendritic phenotypes.

Transheterozygotes for trc1/hpoKC202 exhibit obvious iso-neuronal as well as hetero-neuronal tiling defects, including a significant increase in dendritic crossing-points compared to single mutants.

fry2 trc1 matse235 triple heterozygotes have a weak multiple wing hair phenotype in 48% of wings.

fry1/trc1 larvae exhibit tiling defects, though they have normal dendritic length and branch points.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (4)
Notes on Origin
Discoverer

A. Ferrus.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
References (18)