Mutation results in a truncated protein that lacks the C-terminal 105 amino acids of the wild-type protein.
Nucleotide substitution: G1532A.
Amino acid replacement: W210term.
G16857047A
G1532A
W210term | sina-PA; W210term | sina-PB; W210term | sina-PC
W210term
TGG to TGA
adult abdominal segment 3 & chaeta (with sina3)
adult abdominal segment 3 & microchaeta (with sina3)
adult abdominal segment 3 & tormogen cell | supernumerary (with sina3)
adult abdominal segment 3 & trichogen cell | supernumerary (with sina3)
adult abdominal segment 4 & chaeta (with sina3)
adult abdominal segment 4 & microchaeta (with sina3)
adult abdominal segment 4 & tormogen cell | supernumerary (with sina3)
adult abdominal segment 4 & trichogen cell | supernumerary (with sina3)
mesothoracic tergum & chaeta (with sina3)
mesothoracic tergum & microchaeta (with sina3)
mesothoracic tergum & tormogen cell | supernumerary (with sina3)
mesothoracic tergum & trichogen cell | supernumerary (with sina3)
sina2 homozygous clones in the adult midgut bear virtually no enteroendocrine cells, unlike the expected 6-8% in control clones, but exhibit a similar number of cells as compared to controls.
Mutants show a double- bristle phenotype.
41% of the notal microchaetae and 62% of the microchaetae on abdominal segments 3 and 4 are missing in sina2/sina3 flies. 17.2% of bristles on the notum are duplicated, having 2 hairs emerging from 2 sockets or a fused socket. 44.5% of bristles on abdominal segments 3 and 4 are duplicated (2 hairs/2 sockets) and 20.9% show other defects (including 1 hair surrounded by 2-3 sockets, and 2 socket or 4 socket clusters without shafts). Embryonic development, including development of the es organs, is normal in sina2/sina3 animals.
Proportion of ommatidia with an R7 cell is less than 5%.
Amorph based on the phenotypes of hemizygous <up>sina1/Df(3L)st-g18</up> versus that of homozygous flies.
This allele probably represents complete loss of function of the sina gene. In the ommatidia the R7 photoreceptor cell is always missing, the R7 precursor adopting a cone cell fate, and sometimes one or two cells of the R1-R6 class are missing as well. The normal trapezoidal arrangement of the R1-R6 cells is disorganised, and the R8 cell is often found in uncharacteristic positions. Other adult sensory organs are also affected: sensory bristles distributed over the body surface are frequently missing, with neither the cuticular bristle sheath nor the socket being present, affected sensory organs including the microchaetae and macrochaetae of the head, notum, abdomen and wing margin, and the stout and slender bristles of the anterior wing margin. The phenotype is most severe with bristles located on the abdomen, where often only a minor fraction of the normal number of bristles are present. Also, many of the remaining bristles have two or three sheaths emerging from a single socket. There is also a 10-fold reduction in adult lifespan, and adult behaviour is generally lethargic and uncoordinated. Neither males nor females are fertile, although they produce morphologically normal sperm and eggs, respectively.
sina2 has decreased cell number | somatic clone | adult stage phenotype, suppressible by ttkGD4414/Scer\GAL4Act.PU
sina3/sina2 has photoreceptor cell R1 | third instar larval stage phenotype, enhanceable by msi1/msi1
sina3/sina2 has photoreceptor cell R6 | third instar larval stage phenotype, enhanceable by msi1/msi1
sina3/sina2 has photoreceptor cell R7 | third instar larval stage phenotype, enhanceable by msi1/msi1
sina3/sina2 has external sensory organ phenotype, enhanceable by msi1/msi1
sina2 has enteroendocrine cell | somatic clone | adult stage phenotype, suppressible by ttkGD4414/Scer\GAL4Act.PU
sina2 has adult midgut | somatic clone phenotype, suppressible by ttkGD4414/Scer\GAL4Act.PU
msi1, sina3/sina2 has photoreceptor cell R1 | third instar larval stage phenotype, suppressible by ttkGD4414/Scer\GAL4lz-gal4
msi1, sina3/sina2 has photoreceptor cell R6 | third instar larval stage phenotype, suppressible by ttkGD4414/Scer\GAL4lz-gal4
msi1, sina3/sina2 has photoreceptor cell R7 | third instar larval stage phenotype, suppressible by ttkGD4414/Scer\GAL4lz-gal4
sina3/sina2 has photoreceptor cell R7 phenotype, suppressible by edslH8/ed1X5
sina3/sina2 has ommatidium phenotype, suppressible by edslH8/ed1X5
msi1, sina3/sina2 has ommatidium phenotype, suppressible by ttkosn
msi1, sina3/sina2 has rhabdomere phenotype, suppressible by ttkosn
sina2 has photoreceptor cell R7 phenotype, non-suppressible by sl1
sina2 has photoreceptor cell R7 phenotype, non-suppressible by sl2
sina3/sina2 is an enhancer of external sensory organ phenotype of msi1
sina3/sina2 is an enhancer of ommatidium phenotype of msi1
sina2 is a suppressor of photoreceptor cell R7 phenotype of sty254
sina3/sina2 is a suppressor of eye phenotype of phylGMR.PC
sina2 is a suppressor of phenotype of phylhs.sev
msi1, sina3/sina2, ttkosn has ommatidium phenotype
msi1, sina3/sina2, ttkosn has rhabdomere phenotype
RasGAP1B2, sina2 has photoreceptor cell R7 phenotype
The absence of enteroendocrine cells in adult midgut sina2 clones is suppressed by the clonal expression of ttkGD4414 under the control of Scer\GAL4Act.PU, even leading to their severe increase in number as compared to control clones.
In sina2,msi1/sina3,msi1 mutant third instar larval eye discs significantly reduced numbers of R1 and R6 photoreceptor cells are observed. Very few R7 cells are recruited to the developing ommatidia in these mutants, decreased in number compared to sina2/sina3 mutant animals.
Expression of ttkGD4414 under the control of Scer\GAL4lz-gal4 in sina2,msi1/sina3,msi1 mutant third instar larval eye discs, significantly rescues the number of R1 and R6 cells, although recruitment of these cells appears delayed. Ectopic R7 cells are observed in most developing ommatidia.
Double mutants of sina2/sina3 with msi1 show a synergistic, not additive, eye phenotype. Ommatidial arrays are disturbed, eyes consequently roughened and ommatidia do not contain more than five rhabdomeres. Cone cell array is disturbed. 30% of the ommatidia of sina2 msi1 ttkosn/sina3 msi1 show the normal number and arrangement of photoreceptor cells. The cone cell defects of sina2 msi1/sina3 msi1 are also suppressed by ttkosn.
The phylGMR.PC eye phenotype is completely suppressed in a sina2/sina3 background; the eyes are normal, except for the lack of R7 photoreceptor cells due to the absence of sina function. sina2/sina3 flies carrying both phylGMR.PC and ttk88.GMR.T:Hsap\MYC have very disrupted eyes, similar to those of flies carrying ttk88.GMR.T:Hsap\MYC alone.
Ommatidia of double mutants with Gap1B2 do not have multiple R7 cells.
Ecol\CAT activity in sina2 mutant flies transformed with either Ecol\CATRh3.PF or Ecol\CATRh4.PF is reduced by 90% or eliminated respectively, confirming that R7 was absent from each ommatidium in sina2 mutants. Ecol\lacZ82 expression is abolished in the R7 precursor cell in sina2 mutants.
No interaction with P{sev-svp1} or P{sev-svp2} exists.