Amino acid replacement: A1128V. Amino acid replacement: L1131M.
C3500027T
A1105V | tim-PB; A1104V | tim-PL; A1105V | tim-PM; A1105V | tim-PP; A1073V | tim-PR; A1073V | tim-PS; A1128V | tim-PT; A1105V | tim-PU
A1128V
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two mutations in this line. The difference in the reported and annotated positions of the mutations is due to the use of a downstream translation start (23aa) in the current tim gene annotations.
C3500019A
L1108M | tim-PB; L1107M | tim-PL; L1108M | tim-PM; L1108M | tim-PP; L1076M | tim-PR; L1076M | tim-PS; L1131M | tim-PT; L1108M | tim-PU
L1131M
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two mutations in this line. The difference in the reported and annotated positions of the mutations is due to the use of a downstream translation start (23aa) in the current tim gene annotations.
Under LD conditions, mutant adults behave similarly to wild-type flies in locomotor rhythm assays. The free-running locomotor activity period of homozygous males is 26 hours, 2 hours longer than that of controls. Heterozygous mutants also show a mild lengthening of the locomotor rhythm period under free-running conditions. The free-running eclosion period of mutant animals is the normal 24 hours. Analysis of the phase response curve (PRC) of timblind flies to brief pulses of light indicates that they react with small (1.5 hour) phase delays to light pulses given at ZT15 and ZT17, which normally causes delays of about 3 hours. When the light pulse is given at ZT19, the timblind flies react with a 1 hour phase delay, in contrast to wild-type flies, which react with a 3.5 hour phase advance. At ZT21, the mutant flies show robust phase advances, whereas controls already show a reduction in the amount of phase advances at this time. Overall, the timblind PRC is blunted in the delay portion, and the transition point (where delay changes to advance) is retarded by about 2 hours.
timblind has abnormal locomotor rhythm phenotype, non-enhanceable by sgg[+]/sgg32
timblind has abnormal locomotor rhythm phenotype, non-suppressible by sgg[+]/sgg32
More than 80% of adults expressing sggEP1576 under the control of Scer\GAL4tim.PE in a timblind background rapidly become arrhythmic for locomotor activity after they are placed in constant darkness conditions. The few animals that are rhythmic have a locomotor activity period that is intermediate between that of timblind homozygotes and that of adults expressing sggEP1576 under the control of Scer\GAL4tim.PE in a wild-type background. The increase in locomotor rhythm period length seen in timblind homozygous flies in free-running conditions is not further increased if the flies also carry sgg32.