Deletion of sequences encoding thr amino acids 1031 to 1037.
Females carrying two copies of thrΔVQ.T:Hsap\MYC are fertile at 25oC, but almost completely sterile at 18oC. At 18oC, many eggs are laid but very few larvae hatch. The cold sensitive period occurs during the early stages of embryogenesis; embryos maintained at 25oC for the first 3.5 hours of development and then raised at 18oC hatch. 35% of syncytial embryos derived from females carrying two copies of thrΔVQ.T:Hsap\MYC and raised at 18oC during early development have various irregularities, which include embryonic regions with mitotic asynchrony, abnormal mitotic figures and lower nuclear densities than normal. Many embryos with regular nuclear distribution have fewer nuclei compared to control embryos of the same age. During cellularisation 99% of embryos derived from females carrying two copies of thrΔVQ.T:Hsap\MYC and raised at 18oC during early development lose a large fraction of nuclei from the egg periphery (the nuclei accumulate in the yolk region in the interior of the egg). Cellularisation is delayed in these embryos compared with nuclear elongation. Centrosome separation is impaired and microtubule asters are slightly smaller than normal. Centrosomes and microtubule asters are seen to stay at the cortex above nuclei which are displaced interiorly.
thrΔVQ.Tag:MYC has lethal | maternal effect | embryonic stage | cold sensitive phenotype, suppressible by Sse13m/Sse[+]
thrΔVQ.Tag:MYC has lethal | maternal effect | embryonic stage | cold sensitive phenotype, suppressible by Df(3L)SseA/+
thrΔVQ.Tag:MYC has embryo | maternal effect | embryonic stage 5 phenotype, suppressible by Sse13m/Sse[+]
The maternal effect lethality and cellularisation defects of embryos derived from females carrying two copies of thrΔVQ.T:Hsap\MYC and raised at 18oC are suppressed by one copy of Sse13m; only 7% of these embryos have cellularisation defects. If SseC497S.Scer\UAS.T:Ivir\HA1 is expressed in this background under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16 the frequency and severity of cellularisation defects is unaffected. If, however, SseScer\UAS.T:Ivir\HA1 is expressed in this background under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16, 56% of the embryos have cellularisation defects.
Rescues the embryonic lethality of thr null mutations. The rescued animals hatch with the expected frequency and have no apparent morphological defects.