Somatic clones lacking ft422 display overgrown and altered cell-cell adhesion with characteristic circular and smooth clone borders , unlike the 'wiggly' borders of their wild-type neighbours.
Clones of ft422 mutant cells produce dramatic outgrowths in diverse adult structures such as antennae, thoraxes, wings, and legs. In addition to growing beyond normal tissue size, ft422 mutant cells exhibit a growth advantage over wild-type cells. ft422 FLP-induced mutant clones in the third instar occupy nearly the entire disc tissues in contrast to wild-type clones, which occupy less than half of the discs.
ft422 mutant heads are severely overgrown, with slightly bigger but deformed eyes and duplications of ventral vibrissae.
ft422 mutant retina exhibit only a few more pigment cells than wild-type, indciating a slight increase in the number of interommatidial cells.
In ft422 null clones, approximately 52.5% of ommatidia, including mosaic and mutant ommatidia, exhibit defects in polarity. Of these 50.5% are inverted on their dorsal ventral (D/V) axis. The remaining 2% of ommatidia are inverted on their anterior posterior axis or on both axes. Furthermore 98% of mosaic ommatidia that are phenotypically mutant are inverted on their D/V axis. Ommatidia inverted on their D/V axis preferentially localise toward the polar border such that the phenotypically mutant ommatidia are found in the polar region of the clone and phenotypically wild-type ommatidia are found along the equatorial border. This leads to the formation of an "inverted equator" within the clone, in which the points of opposing trapezoids face each other. Inverted equators consistently arise approximately 2 rows from the equatorial border of the clone. ft422 clones in the eye occasionally lie along the equator but are not seen top cross it. In homozygous mutant eyes (generated by mitotic recombination using the "EGUF/hid method") the dorsal ventral axis is so severely perturbed that the endogenous equator is abolished. When ommatidia are examined that are mosaic (with respect to ft422) in the pair of photoreceptor cells, R3 and R4, 82% of the time the mutant cell is R4 and the wild-type cell R3. When the pair R2 and R5 are examined, 75% of the time the mutant cell is R5 and the wild-type cell R2. When the pair R1 and R6 are examined, 81% of the time the mutant cell is R6 and the wild-type cell R1.
ft8/ft422 has abnormal size | third instar larval stage phenotype, enhanceable by wtsx1/wts[+]
ft8/ft422 has lethal - all die before end of pupal stage phenotype, suppressible | partially by yki[+]/ykiB5
ft422 has abnormal cell growth | somatic clone phenotype, suppressible | partially by exUAS.cBa/Scer\GAL4GMR.PF
ft8/ft422, yki[+]/ykiB5 has visible | adult stage phenotype
ft8/ft422, yki[+]/ykiB5 has abnormal size | adult stage phenotype
exBQ, ft422 has abnormal size phenotype
ft8/ft422 has wing disc | third instar larval stage phenotype, enhanceable by wtsx1/wts[+]
ft8/ft422 has eye disc | third instar larval stage phenotype, enhanceable by wtsx1/wts[+]
ft422 has eye | somatic clone phenotype, non-enhanceable by dsUAO71
ft422 has interommatidial bristle | somatic clone phenotype, non-enhanceable by dsUAO71
ft422 has pigment cell | somatic clone phenotype, non-enhanceable by dsUAO71
ft8/ft422 has wing disc | third instar larval stage phenotype, suppressible by yki[+]/ykiB5
ft8/ft422 has eye disc | third instar larval stage phenotype, suppressible by yki[+]/ykiB5
ft422 has eye | somatic clone phenotype, suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has interommatidial bristle | somatic clone phenotype, suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has pigment cell | somatic clone phenotype, suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has adult antennal segment | somatic clone phenotype, non-suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has adult thorax | somatic clone phenotype, non-suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has wing | somatic clone phenotype, non-suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has leg | somatic clone phenotype, non-suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has adult head | somatic clone phenotype, non-suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 has vibrissal bristle | somatic clone phenotype, non-suppressible by exUAS.cBa/Scer\GAL4GMR.PF
ft422 is an enhancer of interommatidial bristle phenotype of Mer4
ft422 is a non-enhancer of interommatidial bristle phenotype of exBQ
ft8/ft422, yki[+]/ykiB5 has eye | adult stage phenotype
ft8/ft422, yki[+]/ykiB5 has wing | adult stage phenotype
ft8/ft422 mutants, heterozygous for wtsx1 exhibit a significant increase in size, both from wild-type and the ft8/ft422 double mutant, and display an even more 'rippled' morphology.
ft8/ft422 mutants, heterozygous for ykiB5 exhibit a size and morphology similar to those of wild-type discs, indicating suppression of the ft8/ft422 phenotype through ykiB5.
ft8/ft422 mutants, heterozygous for ykiB5 progress to the late pupal stage of development, with some surviving to adulthood. ft8 ykiB5/ft422 flies display defects in the size and morphology of eyes, wings, and some bristles.
Overexpression of exScer\UAS.cBa in the developing eyes of ft422 mutant heads, under the control of Scer\GAL4GMR.PF results in small and rough eyes, very similar to the overexpression of exScer\UAS.cBa in a wild-type background, indicating that exScer\UAS.cBa expression suppresses the ft422 mutant eye phenotype. ft422 mutant phenotypes, such as extra vibrassae, are still observed in the head cuticle, where exScer\UAS.cBa is not overexpressed (under the control of Scer\GAL4GMR.PF).
ft422;Mer4 double mutants exhibit a large excess of interommatidial cells, in a very similar manner to hpo mutants.
ft422;exBQ double mutant retinae do not exhibit large numbers of interommatidial cells and resemble the exBQ and ft422 single mutant phenotypes. However, ft422;exBQ double mutant clones exhibit stronger overgrowth phenotypes than the single mutants in the head outside the retina, that ft and ex may also have functions independent of each other.
dsUAO71 mutants do not significantly enhance the extra ommatidial cell phenotype of ft422 mutants.