Point mutation. Amino acid replacement: R48C. Nucleotide substitution: C142T.
C3194640T
C142T
R48C | Hsp83-PA; R48C | Hsp83-PB
R48C
Hsp8313F3 has no effect on an invariant bristle trait (thoracic and scutellar bristles were analysed). Hsp8313F3 has no significant effect on the trait mean of a variable bristle trait (the sternopleural, orbital, ocellar and vibrissa and carina bristles were analysed) compared to the background strain in which the Hsp8313F3 mutation was induced.
Viable in transheterozygous combination with either Hsp83e1D or Hsp83e3A; males are sterile and females are weakly fertile. Viable in transheterozygous combination with Hsp83e6A; males and females are sterile. Hsp83e1D/Hsp8313F3 and Hsp8313F3/Hsp83e3A 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 interacts genetically with the sev mutations; 'sev315' and sevS11.T:Hsap\MYC.
Hsp83[+]/Hsp8313F3 is a suppressor of photoreceptor cell R7 | ectopic phenotype of Raf::tor12D.hs.sev
Hsp8313F3 is a suppressor of eye phenotype of Raf::tor12D.sev
Presence of Hsp8313F3 completely eliminates all additional R7 cells in phl::tor12D.hs.sev mutants.
Dominantly suppresses the rough eye phenotype of phl::tor12D.sev.
Hsp8313F3 is rescued by Hsp83+t7.5
Lethality can be rescued by Hsp83+t7.5. Hsp83+t7.5 also rescues the dominant suppression phenotype. Transheterozygotes with Hsp83e6D or Hsp83e4A are viable and result in male sterility with no other signs of abnormal development.
Hsp8313F3 and Hsp8319F2 are independent isolates of the same point mutation.