Amino acid replacement: W374term.
G24096417A
W374term | gek-PA
W374term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
eye (with Df(2R)e03819-f02302), with Scer\GAL4Glass38-1, gekΔCC.UAS
lamina | third instar larval stage (with Df(2R)e03819-f02302), with Scer\GAL4Glass38-1, gekΔCC.UAS
lamina | third instar larval stage (with Df(2R)e03819-f02302), with Scer\GAL4Glass38-1, gekΔCH.UAS
lamina | third instar larval stage (with Df(2R)e03819-f02302), with Scer\GAL4Glass38-1, gekΔPH.UAS
Homozygous eye-specific gekomb1080 clones (generated using the eyFLP method) cause specific defects in R cell axon target selection in adult flies. The cartridges (barrel-like structures of 6 post-synaptic axon targets) are disorganised in gekomb1080 mutants, with individual cartridges displaying variable numbers of axon terminals. As in wild type, the majority of R1-R6 axons target to the lamina and only rare fibers extend into the medulla. 96% of R7 axons and 99% of mutant R8 axons innervate the correct layer in the medulla compared to 100% in controls.
In both homozygous gekomb1080 and transheterozygous gekomb1080/Df(2R)e03819-f02302 third instar larval R cell axon fascicles above the lamina plexus are occasionally clumped and the lamina plexus appears broken and varies in thickness. This phenotype is seen in all brains examined. Additionally, occasional bundles of axons are observed extending into the medulla that are thicker than usual. A slightly increased number of R2-R5 cell axons project into the medulla in gekomb1080/Df(2R)e03819-f02302 compared to wild type. Animals in which only R cells are homozygous for gekomb1080 (using eyFLP clones) exhibit a similar but weaker phenotype. No transformations of R1-R6 neurons into R7-R neurons are observed in homozygous gekomb1080 eye discs.
Homozygous gekomb1080 pupal stage R cell clones extend out of the retina into the brain, fasciculate normally and stop in the lamina. However, once in the lamina, mutant photoreceptors often make errors in columnar targeting, making projections to one or more incorrect target cartridges in addition to the correct target or failing to extend at all. Only 35% of R cells make the correct extension, 35% mistarget and 30% fail to extend. Targeting errors are observed in all R1-R6 cells. Homozygous gekomb1080 R cell growth cones display 20% fewer filopodia and are approximately 30% smaller than corresponding control growth cones. The ommatidia appear morphologically normal.
In gekomb1080/gekNP5192 third instar larvae R cell axon fascicles above the lamina plexus are occasionally clumped and the lamina plexus appears broken and varies in thickness. This phenotype is seen in all brains examined. Additionally, occasional bundles of axons were observed extending into the medulla that are thicker than usual.
Expression of gekΔCC.Scer\UAS under the control of Scer\GAL4Glass38-1 in gekomb1080/Df(2R)e03819-f02302 mutant third instar larvae results in early termination of many R cell growth cones, with large clumps appearing in the optic stalk and the distal lamina.
Expression of gekΔPH.Scer\UAS under the control of Scer\GAL4Glass38-1 in gekomb1080/Df(2R)e03819-f02302 mutant third instar larvae results in early termination of many R cell growth cones, with large clumps appearing in the optic stalk and the distal lamina.
Expression of gekΔCH.Scer\UAS under the control of Scer\GAL4Glass38-1 in a gekomb1080/Df(2R)e03819-f02302 mutant third instar larvae results in early termination of many R cell growth cones, with large clumps appearing in the optic stalk and the distal lamina.
gek[+]/gekomb1080 is a suppressor | partially of egg chamber phenotype of RhoGAP19Dunspecified
gekomb1080 is rescued by Scer\GAL4elav-C155/gekUAS.cGa
gekomb1080 is rescued by Scer\GAL4elav-C155/gekΔISP.UAS
gekomb1080/Df(2R)e03819-f02302 is rescued by gekUAS.cGa
gekomb1080/Df(2R)e03819-f02302 is rescued by gekΔCRIB.UAS
gekomb1080/Df(2R)e03819-f02302 is rescued by gekΔCR.UAS
gekomb1080 is partially rescued by Scer\GAL4elav-C155/gekΔCC.UAS
gekomb1080 is partially rescued by Scer\GAL4elav-C155/gekΔPH.UAS
gekomb1080/Df(2R)e03819-f02302 is not rescued by gekK129A.UAS
gekomb1080/Df(2R)e03819-f02302 is not rescued by gekΔSTK.UAS
Expression of gekScer\UAS.cGa under the control of Scer\GAL4Glass38-1 rescues the axon targeting phenotypes seen in gekomb1080/Df(2R)e03819-f02302 third instar larvae.
Expression of gekΔSTK.Scer\UAS under the control of Scer\GAL4Glass38-1 fails to rescue the axon targeting phenotypes seen in gekomb1080/Df(2R)e03819-f02302 third instar larvae.
Expression of gekK129A.Scer\UAS under the control of Scer\GAL4Glass38-1 fails to rescue the axon targeting phenotypes seen in gekomb1080/Df(2R)e03819-f02302 third instar larvae, with animals frequently displaying a severe phenotype.
Expression of gekΔCR.Scer\UAS under the control of Scer\GAL4Glass38-1 rescues the axon targeting phenotypes seen in gekomb1080/Df(2R)e03819-f02302 third instar larvae, with animals frequently displaying a severe phenotype.
Expression of gekScer\UAS.cGa in R cells under the control of Scer\GAL4elav-C155 rescues the axon targeting phenotypes seen in gekomb1080 homozygous pupal stage clones. 91% of axons extend correctly, only 3% mistarget and 6% do not extend. Premature stopping of R1-R6 axons above the lamina plexus is not observed.
Expression of gekΔCC.Scer\UAS in pupal stage R cells under the control of Scer\GAL4elav-C155 rescues the axon targeting phenotypes seen in gekomb1080 homozygous clones. 84% of axons extend correctly, 4% mistarget and 12% do not extend. Premature stopping of R1-R6 axons above the lamina plexus was not observed. However, approximately 18% of R cells exhibit morphological defects, with apical domains extending too far towards the center of the ommatidium or being located basally. 6% of all R cell bodies are below the plane of the ommatidium. All remaining R cells appear normal.
Expression of gekΔPH.Scer\UAS in pupal stage R cells under the control of Scer\GAL4elav-C155 rescues the axon targeting phenotypes seen in gekomb1080 homozygous clones. 83% of axons extend correctly, 12% mistarget and 5% do not extend. Premature stopping of R1-R6 axons above the lamina plexus is not observed. However, approximately 18% of R cells exhibit morphological defects, with apical domains extending too far towards the center of the ommatidium or being located basally. 6% of all R cell bodies are below the plane of the ommatidium. All remaining R cells appear normal.
Expression of gekΔCRIB.Scer\UAS under the control of Scer\GAL4Glass38-1 rescues the axon targeting phenotypes seen in gekomb1080/Df(2R)e03819-f02302, with animals frequently displaying a severe phenotype.
Expression of gekΔISP.Scer\UAS under the control of Scer\GAL4Glass38-1 rescues the axon targeting phenotypes seen in gekomb1080/Df(2R)e03819-f02302, with animals frequently displaying a severe phenotype.
Expression of gekΔISP.Scer\UAS in R cells under the control of Scer\GAL4elav-C155 rescues the axon targeting phenotypes seen in gekomb1080 homozygous clones.