18bp in-frame deletion; removes six amino acid residues (MQLHLA) within the 10th zinc-finger motif (this is within a putative Mad protein-binding motif).
18bp in-frame deletion; removes six amino acid residues (MQLHLA) within the 10th zinc-finger motif of L.
abnormal size (with Lfee)
lethal (with Df(2R)BSC11)
lethal (with Df(2R)BSC357)
lethal (with Df(2R)BSC668)
lethal (with Df(2R)ED2354)
lethal (with Df(2R)trix)
viable (with Df(2R)03072)
viable (with Df(2R)BSC700)
viable (with Df(2R)Exel8059)
40-80% of heterozygotes have weak eye phenotypes, such as small dents in the anterior part of the eye.
Lrev6-3 clones in they eye disc show TUNEL-positive cells in the ventral eye (indicating cell death), while cells in the dorsal half of the eye are not affected.
Heterozygotes have normal eyes. Homozygous clones in the eye result in elimination of the ventral eye, but have no effect in the dorsal eye.
Homozygous clones in the dorsal part of the eye do not affect ommatidial development. Homozygous clones in the ventral part of the eye inhibit ommatidial development. Homozygous clones generated during the first larval instar can completely eliminate eye fate in the eye-antennal disc, whereas antennal development in the same disc is unaffected.
Homozygous embryos fail to complete germ band retraction and show no cuticle formation. Homozygous clones in the ventral part of eye disc, induced during the first larval instar, result in a large reduction of the ventral part of the eye disc in the third larval instar, with the surrounding heterozygous tissue and wild-type clonal tissue generally disappearing together with the homozygous clonal tissue. This results in adult eyes in which most of the ventral region of the eye is replaced by the cuticle. Homozygous clones of considerable size in the dorsal part of the eye disc, induced during the first larval instar, do not cause any obvious reduction in size of the dorsal part of the eye disc, and photoreceptor differentiation and polarity appears unaffected by these clones. Homozygous clones induced in ventral or dorsal regions of the eye disc during the late second and the third larval instars do not result in any obvious eye defects.
Lrev6-3 has increased cell death | somatic clone | larval stage phenotype, suppressible by Scer\GAL4ey.PH/sggS9A.UAS
Lrev6-3 has increased cell death | somatic clone | larval stage phenotype, suppressible by panΔN.UAS/Scer\GAL4ey.PH
Lrev6-3 has visible | recessive | somatic clone phenotype, suppressible by pnr[+]/pnrVX6
L[+]/Lrev6-3 is a suppressor of visible | somatic clone phenotype of pnrVX6
Lrev6-3 has eye | somatic clone phenotype, suppressible by hth[+]/hthMeis1-P2
Lrev6-3 has eye disc | somatic clone phenotype, suppressible by hth[+]/hthMeis1-P2
Lrev6-3 has eye | somatic clone phenotype, suppressible by hth[+]/hth100-1
Lrev6-3 has eye disc | somatic clone phenotype, suppressible by hth[+]/hth100-1
Lrev6-3 has eye disc | ventral | somatic clone phenotype, suppressible by Scer\GAL4ey.PH/sggS9A.UAS
Lrev6-3 has eye disc | ventral | somatic clone phenotype, suppressible by panΔN.UAS/Scer\GAL4ey.PH
Lrev6-3 has eye | ventral | somatic clone phenotype, suppressible by pnr[+]/pnrVX6
L[+]/Lrev6-3 is a suppressor of eye | dorsal | somatic clone phenotype of pnrVX6
Lrev6-3 heterozygous eye clones in a hth100-1 or hthMeis1-P2 heterozygous background results in no ventral eye loss and a wild-type eye phenotype.
Expression of either sggS9A.Scer\UAS or panΔN.Scer\UAS, under the control of Scer\GAL4ey.PH, in Lrev6-3 clones suppresses the loss of ventral cells in the eye disc.