Amino acid replacement: R395P.
G19832341C
R391P | trc-PA; R395P | trc-PB
R395P
Position of mutation on reference sequence inferred by FlyBase curator. Difference in amino acid position due to slightly different predicted cds used by authors.
arista lateral (with trc8)
denticle (with Df(3L)kto2)
multidendritic neuron & dendrite
multidendritic neuron & dendrite | somatic clone
multidendritic neuron & dendrite | supernumerary
wing hair | somatic clone | increased number (with trc8)
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).
Df(2R)Sema2b-C4, trc1 has abnormal neuroanatomy | third instar larval stage phenotype
rawjj102, trc1/trc[+] has abnormal neuroanatomy | somatic clone phenotype
Mob2H4-5, trc1/trc[+] has abnormal neuroanatomy | third instar larval stage phenotype
stan[+]/stanE59, trc1 has abnormal neuroanatomy | third instar larval stage phenotype
mTorΔP, trc1/trc[+] has abnormal neuroanatomy phenotype
Sin1e03756, trc1/trc[+] has abnormal neuroanatomy phenotype
rictorΔ2, trc1/trc[+] has abnormal neuroanatomy phenotype
hpoMGH4, trc1/trc[+] has abnormal neuroanatomy phenotype
hpoKC202, trc1/trc[+] has abnormal neuroanatomy phenotype
hpoMGH4/hpo[+], trc1 has abnormal neuroanatomy phenotype
hpoKC202/hpo[+], trc1 has abnormal neuroanatomy phenotype
fry2/fry[+], matse03077, trc1/trc[+] has visible | dominant phenotype
Df(2R)Sema2b-C4, trc1 has dendrite | third instar larval stage phenotype
rawjj102, trc1/trc[+] has dendrite | somatic clone phenotype
rawjj102, trc1/trc[+] has larval multidendritic class IV neuron | somatic clone phenotype
Mob2H4-5, trc1/trc[+] has NMJ bouton | third instar larval stage phenotype
Mob2H4-5, trc1/trc[+] has embryonic/larval neuromuscular junction | third instar larval stage phenotype
stan[+]/stanE59, trc1 has dendrite | third instar larval stage phenotype
stan[+]/stanE59, trc1 has larval dorsal multidendritic neuron ddaC | third instar larval stage phenotype
Sin1e03756, trc1/trc[+] has dendrite phenotype
Sin1e03756, trc1/trc[+] has larval multidendritic class IV neuron phenotype
mTorΔP, trc1/trc[+] has larval multidendritic class IV neuron phenotype
rictorΔ2, trc1/trc[+] has larval multidendritic class IV neuron phenotype
hpoMGH4, trc1/trc[+] has multidendritic dendrite phenotype
hpoKC202, trc1/trc[+] has multidendritic dendrite phenotype
hpoMGH4/hpo[+], trc1 has multidendritic dendrite phenotype
hpoKC202/hpo[+], trc1 has multidendritic dendrite phenotype
fry2/fry[+], matse235, trc1/trc[+] has wing hair | increased number phenotype
fry2/fry[+], matse03077, trc1/trc[+] has wing hair | increased number phenotype
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.
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.
trc1 is rescued by trcUAS.Tag:FLAG/Scer\GAL4477
trc1 is not rescued by trcK122A.UAS.L.Tag:FLAG/Scer\GAL4477
trc1 is not rescued by trcS292A.T449A.UAS.Tag:FLAG/Scer\GAL4477
A. Ferrus.