Nucleotide substitution: G?A. The nucleotide substitution is in intron 6 which generates a cryptic splice acceptor site, which results in a C-terminally truncated mRNA.
G7535530A
G?A
This mutation creates a cryptic splice acceptor which adds 12 bases from the intron onto the subsequent exon.
eye photoreceptor cell & ommatidium | ectopic
Homozygous eyes are rough and many ommatidia contain an abnormal number of photoreceptor cells.
The ommatidia of lqfFDD9 homozygous adults have extra photoreceptors.
Homozygotes are nearly wild-type at 18oC but have eye and wing defects at 25oC. At 25oC, the eyes contain facets with ectopic photoreceptor cells. The additional photoreceptor cells arise from the 'mystery cells' which are present early during eye development. Wings have thickenings of the longitudinal veins and clumps of bristles and notching at the wing margin. Legs have fused and shortened tarsal segments. Second and third legs have defects similar to those in the first legs and a variety of bristle duplications are also seen. lqfFDD9/lqfS011027 flies have similar but more severe phenotypes than those of lqfFDD9 homozygotes. When homozygous lqfFDD9 clones are induced in the eye, phenotypically mutant facets at the clone border containing ectopic photoreceptors are seen in which each photoreceptor, including the ectopic one, is lqf+.
lqfFDD9 has ommatidium phenotype, suppressible by Rala[+]/RalaEE1
lqfFDD9 has eye photoreceptor cell phenotype, suppressible by Rala[+]/RalaEE1
lqfFDD9 has ommatidium phenotype, suppressible by Rala[+]/RalaPG69
lqfFDD9 has eye photoreceptor cell phenotype, suppressible by Rala[+]/RalaPG69
lqfFDD9 has eye phenotype, suppressible by Hsap\EPN2ΔENTH.ro
lqfFDD9 has eye phenotype, suppressible by Hsap\EPN2ro.PO
lqfFDD9 has eye phenotype, suppressible by Rnor\Epn1ΔENTH.ro
lqfFDD9 has eye phenotype, suppressible by Rnor\Epn1ro.PO
The eye defects of lqfFDD9 homozygotes are dominantly enhanced by Chc4. The Chc1/+ ; lqfFDD9/lqfFDD9 combination is lethal. Rare escapers have severely malformed eyes and tarsal fusions and the wing phenotype is enhanced compared to lqfFDD9 homozygotes. The eye and wing defects of lqfFDD9 homozygotes are dominantly enhanced by α-Adaptin3. The lqfFDD9 phenotype is enhanced if the flies are also homozygous for shi1 or shi2.
lqfFDD9 is rescued by lqfΔENTH.GFP
lqfFDD9 is rescued by lqfΔCBM.GFP
lqfFDD9 is rescued by lqfΔDPW.GFP
lqfFDD9 is rescued by lqfΔNPF.GFP
lqfFDD9 is rescued by lqfΔUIM2.GFP
lqfFDD9 is rescued by lqfUIM1.EA.GFP
lqfFDD9 is rescued by lqfΔCBM.ΔDPW1.GFP
lqfFDD9 is rescued by lqfΔCBM.ΔDPW.GFP
lqfFDD9 is rescued by lqf4xNPF.GFP
lqfFDD9 is rescued by lqfENTH.RA.GFP
lqfFDD9 is rescued by lqfENTH.TD.GFP
lqfFDD9 is rescued by lqfENTH.FTVF.RDAA.GFP
lqfFDD9 is rescued by lqfro.Tag:FLAG
lqfFDD9 is rescued by lqfΔDPW.ro.Tag:FLAG
lqfFDD9 is rescued by lqfΔEN2.ro.Tag:FLAG
lqfFDD9 is rescued by lqfΔCBM.ro.Tag:FLAG
lqfFDD9 is partially rescued by lqfΔUIM.GFP
lqfFDD9 is partially rescued by lqfUIM1.EA.ΔUIM2.GFP
lqfFDD9 is partially rescued by lqfENTH.RWRK.AAAA.GFP
lqfFDD9 is partially rescued by lqfΔEN1.ro.Tag:FLAG
lqfFDD9 is partially rescued by lqfΔENTH.ro.Tag:FLAG
lqfFDD9 is partially rescued by lqfENTH.ro.Tag:FLAG
lqfFDD9 is partially rescued by lqfro.Tag:FLAG
lqfFDD9 is not rescued by lqfENTH.UIM.GFP
lqfΔENTH.T:Avic\GFP completely rescues the morphological defects of lqfFDD9 flies.
lqfΔUIM.T:Avic\GFP only slightly rescues the morphological defects of lqfFDD9 flies, with 70 +/- 4% of facets in the eye appearing wild type.
lqfENTH.RWRK.AAAA.T:Avic\GFP only slightly rescues the morphological defects of lqfFDD9 flies, with 16 +/- 5% of facets in the eye appearing wild type.
Allelic series based on viability: lqfFDD9 < lqfbE248 < lqfS011027 < lqfBT < lqfARI = lqfL895 = lqfL71.