C15240062T
Q600term | tefu-PB
Q600term
Position of mutation on reference sequence inferred by FlyBase curator.
The brains of tefuatm-3 homozygote male third instar larvae (treated with colchicine and hypotonic solution) show a significant increase in the frequency of chromosomal aberrations compared to wild-type.
Mosaic eyes produced by the EGUF/Hid method are reduced in size compared to wild type.
Neuroblasts in the brain of homozygous larvae show chronic spontaneous chromosome aberrations (12.5% fused chromosomal arms, 1.6% double-strand breaks).
Homozygous pupae have variable morphological defects affecting the antennae, eyes, bristles, wings and legs. tefuatm-3/tefuatm-6 larval neuroblasts show an extremely high rate of spontaneous chromosomal aberrations. The most frequent defects are telomere fusions (seen in more than 50% of metaphase figures). Both single- and double-telomere associations are seen, including sister and nonsister fusions of homologous chromosomes, as well as fusions between nonhomologous chromosomes. Acentric chromosome fragments are occasionally seen, as are chromosomal transpositions involving the loss of whole chromosome arms. Chromosomal bridges are often seen in anaphase figures.
tefuatm-3 has abnormal DNA repair | larval stage phenotype, enhanceable by TctpEY09182
tefuatm-3 has abnormal cell cycle | larval stage phenotype, enhanceable by TctpEY09182
tefuatm-3 has visible | somatic clone phenotype, suppressible by TctpUAS.cHa/Scer\GAL4ey.PH
tefuatm-3 has visible | somatic clone phenotype, non-suppressible by TctpE12V.UAS/Scer\GAL4ey.PH
tefuatm-3/tefuatm-3 is a non-suppressor of abnormal neuroanatomy | larval stage phenotype of Top2suo3/Df(2L)Exel9043
Tctph59/Tctp[+], tefuatm-3 has abnormal developmental rate | dominant phenotype
tefuatm-3 has chromosome | third instar larval stage | male phenotype, enhanceable by Top2suo1/Top2suo3
tefuatm-3 has larval brain | third instar larval stage | male phenotype, enhanceable by Top2suo1/Top2suo3
tefuatm-3 has eye | somatic clone phenotype, suppressible by TctpUAS.cHa/Scer\GAL4ey.PH
tefuatm-3 has eye | somatic clone phenotype, non-suppressible by TctpE12V.UAS/Scer\GAL4ey.PH
tefuatm-3/tefuatm-3 is an enhancer of larval brain | third instar larval stage | male phenotype of Top2suo1/Top2suo3
tefuatm-3/tefuatm-3 is a non-suppressor of larval brain | third instar larval stage phenotype of Top2suo3/Df(2L)Exel9043
The increased frequency of chromosomal aberrations in third instar larval brain cells characteristic for Top2suo3/Top2suo1 and tefuatm-3/tefuatm-3 single mutant males is enhanced further in Top2suo3/Top2suo1;tefuatm-3/tefuatm-3 double mutants.
The low mitotic index observed in Top2suo3/Df(2L)Exel9043 third instar larval brains cannot be rescued by combination with either mei-4129D or tefuatm-3/tefuatm-3.
tefuatm-3/Tctph59 double heterozygotes show a 2 day delay in the start of pupation compared to either wild-type controls or either single heterozygote.
Expression of TctpScer\UAS.cHa under the control of Scer\GAL4ey.PH strongly suppresses the reduced eye phenotype seen in tefuatm-3 mosaic eyes produced by the EGUF/Hid method.
Expression of TctpE12V.Scer\UAS under the control of Scer\GAL4ey.PH does not suppress the reduced eye phenotype seen in tefuatm-3 mosaic eyes produced by the EGUF/Hid method.
Homozygosity for TctpEY09182 enhances the chromosome aberrations seen in brain neuroblasts of tefuatm-3 larvae (18.0% fused chromosomal arms, 7.9% double-strand breaks).