abnormal locomotor behavior (with Df(3R)d189), with moium.t4.6
short lived (with Df(3R)d189), with moium.t4.6
viable (with Df(3R)d189), with moium.t4.6
adult thoracic sensillum (with Df(3R)d189), with moium.t4.6
chromosome, telomeric region (with Df(3R)d189), with moium.t4.6
eye (with Df(3R)d189), with moium.t4.6
wing margin (with Df(3R)d189), with moium.t4.6
wing vein (with Df(3R)d189), with moium.t4.6
P{lacW}moiS096713/Df(3R)d189 animals carrying P{CaSpeR-DTLum} (i.e. moi mutants) eclose and survive for a short time, exhibiting signs of locomotor defects, rough eyes, missing wing veins, scalloped wings and missing thoracic bristles.
Mitotic cells from the brains of moi1/moiS096713 and and moiS096713/moiCB02140 larvae show frequent telomere fusions.
Flies homozygous for the P{lacW}moiS096713 insertion die as third instar larvae.
Homozygotes die as third instar larvae.
Df(3R)d189/moiS096713, moium.t4.6 has short lived phenotype, enhanceable by tefuatm-6
moium.t4.6, Df(3R)d189, moiS096713 is an enhancer of lethal - all die before end of P-stage phenotype of tefuatm-6
Df(3R)d189/moiS096713, moium.t4.6 has chromosome phenotype, enhanceable by tefuatm-6
Df(3R)d189/moiS096713, moium.t4.6 has chromosome phenotype, suppressible by mei-41RT1
moium.t4.6, Df(3R)d189, moiS096713 is an enhancer of chromosome phenotype of tefuatm-6
tefuatm-6 flies that also carry P{lacW}moiS096713/Df(3R)d189, P{CaSpeR-DTLum} (i.e. moi mutants) die at an earlier phase than either single mutant condition.
tefuatm-6 neuroblasts that also carry P{lacW}moiS096713/Df(3R)d189, P{CaSpeR-DTLum} (i.e. moi mutants) show an increased number of anaphase chromosome bridges than either single mutant condition.
P{lacW}moiS096713/Df(3R)d189, P{CaSpeR-DTLum} (i.e. moi mutant) neuroblasts show fewer anaphase chromosome bridges when mei-41RT1 is present.
Df(3R)d189/moiS096713 is rescued by moi+t4.6
moi1/moiS096713 is rescued by moiR1.Tub
moi1/moiS096713 is rescued by moiR2.Tub
moi1/moiS096713 is rescued by moiR3.Tub
Df(3R)d189/moiS096713 is not rescued by moidm.t4.6
P{CaSpeR-DTL} (expressing wild type moi and Tgs1) rescues the lethality of P{lacW}moiS096713/Df(3R)d189.
The presence of P{CaSpeR-DTLdm} (expressing wild type moi) does not change the lethality phase of P{lacW}moiS096713/Df(3R)d189.
The P3-P4 early pupal lethality seen in P{lacW}moiS096713/Df(3R)d189 animals is completely rescued by P{CaSpeR-DTL} (which carries moi+t4.6 and tatl+t4.6).
The P3-P4 early pupal lethality seen in P{lacW}moiS096713/Df(3R)d189 animals is not rescued by P{CaSpeR-DTLdm} (which carries tatldm.t4.6 and moidm.t4.6).
The P3-P4 early pupal lethality seen in P{lacW}moiS096713/Df(3R)d189 animals is partially rescued by P{CaSpeR-DTLum} (which carries tatlum.t4.6 and moium.t4.6); animals die as pharate adults or immediately after hatching.
The P3-P4 early pupal lethality seen in P{lacW}moiS096713/Df(3R)d189 animals is completely rescued by P{CaSpeR-DTLdm} and P{CaSpeR-DTLum} together in trans.
Associated with: tatlS096713.
The P{lacW}moiS096713 insertion maps upstream of a dicistronic locus that encodes moi (upstream ORF) and tatl (downstream ORF). Rescue analysis indicates that the telomere fusion phenotype seen in P{lacW}moiS096713 mutants is due to an effect on the moi ORF and not on tatl. In contrast, the lethality caused by the insertion is not rescued by a transgene containing either ORF alone, but is rescued by a transgene containing functional copies of both ORFs, indicating that the lethality is due to an effect on both ORFs.
Allelic series (with respect to severity of telomere fusion phenotype): moi1 > moiCB02140 = moiM12 > moiS096713.