Imprecise excision of locoEY04589 generates locoP283, in which nucleotides -310 to +2195 of the transcript (start point of loco-c1 transcript is +1) are depleted, removing the RGS domain, two RBD domains, and the GoLoco motif.
neuroblast (with locoP237)
spindle & mitotic domain 9
locoP283 homozygotes are viable and display severe locomotion defects. locoP283 embryos, lacking both maternal and zygotic components exhibit defects in mitotic spindle orientation. In cells of mitotic domain 9, the mitotic spindle that normally rotates by 90o to align along the apical/basal axis in wild-type often fails to re-orientate. The vast majority of locoP283 mutant neuroblasts, lacking both maternal and zygotic components, divide asymmetrically to produce daughters of different sizes as in wild-type neuroblasts. However, a small proportion (~10%) of locoP283 neuroblasts undergo similar-sized division.
locoP283 has abnormal neuroanatomy phenotype, enhanceable by pinsunspecified
locoP283 has astral microtubule & neuroblast | ectopic phenotype, enhanceable by pinsunspecified
locoP283 has neuroblast phenotype, enhanceable by pinsunspecified
In embryos derived from double germline clones of locoP283 and rapsunspecified, the majority of neuroblasts undergo symmetric divisions to generate two similar-sized daughter cells in stage 10 mutant embryos, in 60% of cases. The cleavage plane is placed near the middle of the two centrosomes and the spindle is positioned symmetrically with both centrosomes lying in close proximity to the cell cortex. Astral microtubules, which are normally associated only with the apical centrosome in wild-type neuroblasts, can emanate from both centrosomes in locoP283 and rapsunspecified double mutant neuroblasts.