Polytene chromosomes normal.
The chromosome containing the gro mutation contains two inserts, one of about 4 kb between coordinates -4.8 and -3.8 kb and a much smaller one at approximately +11.5 detected by Preiss et al. The larger of the two is independent of the gro mutation since Df(3R)Pr4, which deletes the region into which the segment is inserted, does not uncover gro; a similar argument for the independence of the insert at 11.5 can be made since gro is rescued by transformation with a segment from 12.7 to 23.1 (Preiss et al.).
adult head & microchaeta
macrochaeta & abdominal tergite
macrochaeta & head
macrochaeta & thorax
microchaeta & abdominal tergite
microchaeta & head
microchaeta & thorax
The wing phenotype of gro1 heterozygous with deletions for gro is of overgrowth and pattern duplications in regions close to the D/V compartment boundary in the anterior compartment. Weak phenotypes include distal bifurcation of vein LIII and thickening of the proximal costa. Extreme phenotypes consist of overgrowth and pattern duplications in proximal or distal regions of the anterior wing margin, including duplication and triplication of LIII and loss of LII. Sensory elements in affected areas are typical of distal regions of the wing. gro1 when heterozygous with deletions for gro also causes the appearance of clusters of macrochaetae and microchaetae in particular regions of the head, thorax and tergites, though at low frequency.
Homozygotes have clumps of extra bristles above each eye which give impression of bushy eyebrows; also extra bristles on the humerus. Top of head tends to be malformed; ocelli often enlarged and run together. In selected stocks, penetrance approaches 100%, but is low in unselected stocks. Concluded to be an allele of E(spl) on the basis of the visible phenotype of heterozygotes with lethal presumed point mutations at E(spl); however, it does not cause neural hypertrophy and is wild type in combination with E(spl)1.
Ac3EY10141, groC105/gro1 has visible phenotype
CG8924EY00245, groC105/gro1 has visible phenotype
ClampKG00473, groC105/gro1 has visible phenotype
E(spl)m8-HLHrv29, gro1 has lethal phenotype
groC105/gro1 has frontal bristle phenotype, enhanceable by CG12299EY01579
gro1 has ommatidium phenotype, enhanceable by Egfrf13
gro1 has interommatidial bristle phenotype, enhanceable by Egfrf13
gro1 has prothoracic leg phenotype, enhanceable by Egfrf13
gro1 has prothoracic leg phenotype, enhanceable by Egfrt1
gro1 has ommatidium phenotype, enhanceable by Egfrf1
gro1 has interommatidial bristle phenotype, enhanceable by Egfrf1
gro1 has prothoracic leg phenotype, enhanceable by Egfrf1
gro1, Scer\GAL430A is a non-enhancer of wing phenotype of Pka-C1UAS.cKa, Scer\GAL430A
gro1, Scer\GAL430A is a non-suppressor of wing phenotype of Pka-C1UAS.cKa, Scer\GAL430A
Ac3EY10141, groC105/gro1 has frontal bristle phenotype
CG8924EY00245, groC105/gro1 has frontal bristle phenotype
ClampKG00473, groC105/gro1 has frontal bristle phenotype
groE48/gro1, sbb[+]/sbb6 has wing vein L2 phenotype
groE48/gro1, sbb[+]/sbb6 has wing vein L3 phenotype
groE48/gro1, sbb[+]/sbb6 has wing margin bristle phenotype
groE48/gro1, sbb[+]/sbb6 has wing blade anterior compartment phenotype
The overproliferation of frontal bristles on the head that is seen in gro1/groC105 adults is enhanced if they are also hemizygous for CG12299EY01579.
gro1/groC105 ; CG8924EY00245 double mutants have missing frontal bristles in 57% of cases.
gro1/groC105 ; CG1832KG00473/CG1832KG00473 adults have extra frontal bristles on the head in 65% of cases and have missing frontal bristles in 14% of cases.
gro1/groC105 ; Ac3EY10141 double mutants have extra frontal bristles on the head in 55% of cases and have missing frontal bristles in 33% of cases.
gro1/groC105 ; BCL7-likeEY10009/BCL7-likeEY00880 double mutants have extra frontal bristles on the head in 3% of cases and have missing frontal bristles in 96% of cases.
Egfrt1 enhances the bristle, ocellar, wing and limb phenotypes of homozygotes. Bristle hyperplasia, ocellus enlargement and ocellus fusion are enhanced. Wings are notched, wing margins are hairier, have ectopic vein material and anterior outgrowths. Legs are fused and bifurcated. Egfrf1; gro1/gro1 and Egfrf13; gro1/gro1 flies display an enhanced gro phenotype: ectopic compound eyes, fused or bifurcated legs. These phenotypes are almost exclusively restricted to males. The ectopic eyes are organised into arrays of ommatidia. They are frequently adjacent to the endogenous eye but separated by a discrete border and exhibit defects in ommatidial packing and the distribution of interommatidial bristles. Egfrt1/Df(2R)Egfr18; gro1/gro1 flies display a combination of Egfr and gro phenotypes. The L4 wing vein defect is restored and the ocellar bristles are present but disarrayed. In many cases supernumerary ocellar bristles and/or interocellar bristles are present producing a patch of bristles were the ocelli would normally have been. The ocelli are either reduced or eliminated. Most males display one or more ectopic eye structure dorso-medial to the normal eyes. These structures are small and contain discrete ommatidia but no interommatidial bristles. The lens material of these ectopic eyes is fused into a uniform glaze and they are recessed into the head cuticle.
Grell, 64k.