Tarsal defects are not normally seen in legs of homozygous adults.
Mutant antennae show transformation of distal A3 and arista to tarsus.
Mutant flies have a reduced thermosensitivity at the low end, but are normal in their ability to detect temperature differences (3o or 6oC) in the range of their thermosensitivity. In a "heat-box" learning paradigm, mutant flies show avoidance behaviour during training and test phase performance is normal when using a 37oC punishment temperature. When 30oC is used as the punishment temperature, mutant flies show no avoidance behaviour, in contrast to wild type.
Antenna to leg transformation.
Shows mutant temperature gradient response. Flies are partially thermosensitive, and avoid temperatures above 35oC. Behavior with respect to humidity is wild type.
Homozygotes and ssa/ssaP88 flies show transformation of the arista to distal mesothoracic tarsus. Expressivity of the phenotype is higher in ssa/ssaP88 flies than in ssa homozygotes. The expressivity of the phenotype decreases with increasing temperature in ssaB/ssa flies. A high proportion of homozygous or ssa/ssaP88 flies produce an ectopic tarsal response to chemical stimulation at 25oC. ssa/ssaP88 flies usually cannot fly.
The distal region of the antennal disc, the arista, is transformed to the corresponding leg region, the tarsus. The first 2-4 neurons appear in the homeotically transformed antennal disc at the pre-pupal stage, earlier than in wild-type. They are located at the centre of the disc (this region will develop into the tarsus). At 5 hours after puparium formation, the protrusion of the future tarsus is very obvious, and two axonal processes extend from the distal tip towards the antennal part of the disc. Until 10 hours after puparium formation, 2-4 additional neurons develop at the distal end of the tarsus. A cuticular, bag-like protrusion is formed around the homeotic tarsus as soon as it has reached the surface of the ventro-lateral head region. Antennal disc eversion is delayed by approximately 3 hours.
ssa females lack aristae. They are able to distinguish between wild-type males that sing the courtship song, and males without wings that do not sing, and mate more readily with males that sing, suggesting that they can hear the courtship song. The homeotic legs of ssa females are not required for the detection of the courtship song, since females whose homeotic legs have been removeed can still distinguish between singing and non-singing males.
The arista is transformed into a tarsus with mechanosensory bristles.
Antennae and aristae tarsuslike; mean number of tarsal segments = 4.0; incidence of claws = 97.1% (Garcia-Bellido, 1968); classified as an intermediate allele by Struhl. Third joint of antenna like parts of a tarsal row but with broad, flat, plate-like lobes below. Tarsal segments of legs display intermediate level of fusion (Struhl, 1982). Bristles like those of a medium to slight Minute. Frequent extra dorsocentral bristles. Transformed tissue is leg tissue in every attribute tested. Transformed tarsi elicit behavioral response similar to that of normal legs when exposed to sugar solutions (Deak, 1976). Regions of aristae converted into tarsi not affected by mutants affecting aristae (e.g., th and al) but are affected by those operating on tarsi (e.g., fj, d, app and ey) (Waddington, 1939; Braun, 1940; Mglinetz and Ivanov, 1975; Mglinetz, 1976). Dissociated cells from ssa antennal discs aggregate with dissociated leg-disk cells but not with those from wild-type antennal discs (Garcia-Bellido, 1969). Antennal discs from ssa larvae give rise to leg-like structures when transplanted into wild-type hosts as do both duplicated and regenerated antennal discs formed from eye-antenna-disk fragments (Gehring and Schubiger, 1975); when discs are pretreated with colchicine, the developing structures are more aristalike (Vogt, 1947). Homozygous clones of ssa tissue produce antennal leg tissue when induced before (Roberts, 1964) but not after (Postlethwait and Girton, 1974) mid-third instar. Large clones conform to anterior and posterior compartments comparable to those induced in normal mesothoracic legs (Morata and Lawrence, 1979). No maternal effect; temperature independent.
ssa has visible phenotype, suppressible by Scer\GAL4ptc-559.1/danEPgJ3-220
ssa is an enhancer of visible | somatic clone phenotype of ctC145
ssa has arista phenotype, suppressible by Scer\GAL4ptc-559.1/danEPgJ3-220
ssa has tarsal segment | ectopic phenotype, suppressible by Scer\GAL4ptc-559.1/danEPgJ3-220
ssa is an enhancer of arista | somatic clone phenotype of ctC145
ssa is an enhancer of leg | ectopic | somatic clone phenotype of ctC145
Dllmd23, ssa/ss[+] has tarsal segment phenotype
Dllmd23/Dll[+], ssa has tarsal segment phenotype
UbxCbx-1/Ubxbx-1, ssa has mesothoracic tarsal segment phenotype
Ubxbx-3/Ubxbxd-51j, ssa has leg phenotype
Expression of danEPgJ3-220 under the control of Scer\GAL4ptc-559.1 strongly suppresses the arista-to-tarsus transformation seen in ssa flies.
ssa Ubxbx-3 Ubxbxd-51j hemizygotes do not emerge as imagos. Dissection of late pupae reveals flies have four pairs of legs (Ubxbx-3 Ubxbxd-51j phenotype) and the fourth pair of legs exhibit severe disruption of segmentation and an improvement in the segmentation of the third pair. ssa flies carrying Pc3 exhibit 1-2 sex comb teeth on one of the legs of the second and third pair.
Balkaschina, 1926.