Amino acid replacement: S185F. Nucleotide substitution: C?T.
Amino acid replacement: S185F.
C15313006T
C?T
S185F | Tm2-PA; S185F | Tm2-PB; S185F | Tm2-PC; S185F | Tm2-PE; S185F | Tm2-PF; S185F | Tm2-PG
S185F
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Tm2D53/Tm2[+] is a suppressor of abnormal jumping phenotype of wupAhdp-2
Tm2D53/Tm2D53 is a suppressor of abnormal jumping phenotype of wupAhdp-2
Tm2D53 is a suppressor of abnormal locomotor behavior | larval stage phenotype of wupAhdp-2
Tm2D53/Tm2[+] is a suppressor of abnormal locomotor behavior phenotype of wupAhdp-2
Tm2D53/Tm2[+] is a suppressor of abnormal locomotor behavior phenotype of up101
Tm2D53/Tm2[+], up101 has flightless phenotype
Tm2D53/Tm2[+], wupAhdp-2 has abnormal flight phenotype
Tm2D53, wupAhdp-2 has abnormal flight phenotype
Tm2D53, up101 has flightless phenotype
Tm2D53 is a suppressor of indirect flight muscle cell phenotype of MhcS1
Tm2D53/Tm2D53 is a suppressor of indirect flight muscle cell phenotype of wupAhdp-2
Tm2D53/Tm2[+] is a suppressor of indirect flight muscle cell phenotype of wupAhdp-2
Tm2D53/Tm2[+] is a suppressor of somatic muscle cell of leg phenotype of wupAhdp-2
Tm2D53/Tm2D53 is a suppressor of indirect flight muscle cell phenotype of up101
Tm2D53/Tm2[+] is a suppressor of indirect flight muscle cell phenotype of up101
Tm2D53 is a non-suppressor of indirect flight muscle cell phenotype of Mhc13
Tm2D53 is a non-suppressor of indirect flight muscle cell phenotype of wupAhdp-3
Tm2D53 is a non-suppressor of indirect flight muscle cell phenotype of wupAhdp-5
MhcS1/+ structural defects are partially suppressed in Tm2D53 mutants, as the indirect flight muscles of double mutants display less degradation despite the presence of indented thoraces compared to similarly aged MhcS1/+ flies. Tm2D53 suppresses the recessive lethality of MhcS1, increasing homozygote viability from 2.38% to 80.92%.
The hypercontraction of indirect flight muscles seen in wupAhdp-2 flies is completely suppressed by Tm2D53/+. IFMs of 2-3 day old wupAhdp-2 ; Tm2D53/+ flies show an almost complete restoration of wild-type myofibrillar structure. However, some myofibrils show small areas of disorganised filament lattice at their centres. By 6-7 days, all of the myofibrils contain extensive disorganised areas. wupAhdp-2 myofibrillar defects are completely suppressed by Tm2D53/Tm2D53. wupAhdp-2 flies that also carry one or two copies of Tm2D53 hold their wings in the resting position. Young wupAhdp-2 ; Tm2D53/+ or wupAhdp-2 ; Tm2D53/Tm2D53 flies can fly, but less well than wild type. By 6-7 days old, the flight ability of wupAhdp-2 ; Tm2D53/+ but not wupAhdp-2 ; Tm2D53/Tm2D53 flies is dramatically reduced. wupAhdp-2 ; Tm2D53/+ flies show some suppression of the wupAhdp-2 leg muscle phenotype. The larval locomotory and feeding behaviour defects of wupAhdp-2 larvae are suppressed by Tm2D53. The up101 wings-up and IFM phenotypes are completely suppressed by Tm2D53/Tm2D53 and partially suppressed by Tm2D53/+. In both cases, the rescued flies are flightless.