Excision of the progenitor insertion, resulting in a 2742bp deletion that removes the 5' exon of Klp10A.
Hemizygotes arrest development prior to the third instar larval stage.
Oogenesis is completed and eggs are laid in females containing homozygous germline clones, however, the embryos fail to hatch. The mutant embryos show severe disorganisation of both the DNA and microtubules and no structures identifiable as pronuclear fusion or syncytial divisions are observed. Chromosomes are dispersed throughout the cytoplasm and microtubules form large asters surrounding the dispersed chromosomes.
Late-stage oocytes show defects in mutant females. Firstly, spindle microtubule bundles are much longer than in wild type. Secondly, ooplasmic microtubules are more numerous and longer than in wild type and are often arranged in a starburst pattern. Spindle disorganisation ranging from slight (bipolar with some fraying or bending) to extreme (long microtubule bundles with no apparent poles) is seen. The central spindle region is often missing in the mutant oocytes, resulting in two disconnected half spindles and multipolar spindles. The karyosome and spindle are not in proper contact. Bi-orientation of homologous chromosomes is defective.
Klp10A24/Klp10A24 is a non-suppressor | somatic clone of follicle cell | somatic clone phenotype of PatroninEY05252
Klp10A24/Klp10A24 is a non-suppressor | somatic clone of microtubule | somatic clone phenotype of PatroninEY05252
The defective microtubule organization observed in PatroninEY05252 mutant follicle cell clones is not improved upon combination with Klp10A24 in PatroninEY05252;Klp10A24 double mutant clones.
Klp10A24 is rescued by Klp10AUASp.Tag:HA/Scer\GAL4αTub84B.PL
Expression of Klp10AScer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4αTub84B.PL rescues the lethality of Klp10A24 hemizygotes.