Amino acid replacement: S38L. Nucleotide substitution: C113T.
Nucleotide substitution: C113T. Amino acid replacement: S38L.
C3194611T
C113T
S38L | Hsp83-PA; S38L | Hsp83-PB
S38L
Hsp83e1D has no effect on an invariant bristle trait (thoracic and scutellar bristles were analysed). Hsp83e1D has a significant effect on a variable bristle trait (the sternopleural, orbital, ocellar and vibrissa and carina bristles were analysed); there is a significant difference in trait mean compared to the background strain in which the Hsp83e1D mutation was induced.
Viable in transheterozygous combination with either Hsp8313F3 or Hsp839J1; males are sterile and females are weakly fertile. Hsp83e1D/Hsp8313F3 and Hsp83e1D/Hsp839J1 males show defects during spermatogenesis. The number and shape of spermatocytes within 16-cell cysts are mostly normal (5-10% are abnormal). Spermatids with variable number, size and shape of nuclei and nebenkern are seen. Needle-shaped crystals are present throughout developing spermatocytes and spermatids. Individualised sperm are present but they are not motile and are fragile.
Mutation fails to genetically interact with sevS11.T:Hsap\MYC, 'sev351', phl12 or phl::tor12D.hs.sev.
No effect the rough eye phenotype (formation of extra R7 cells) caused by P{sev-svp2} and no effect on the P{ro-svp1} rough eye phenotype (loss of one or more outer photoreceptors from many of the ommatidia).
No interaction with P{sev-svp1} or P{sev-svp2} exists.