Imprecise excision of the progenitor insertion results in a deletion which removes 531 bp of the first exon of mars, including the start codon.
531bp deletion resulting from imprecise excision of P{EP}drkEP2477
When treated with a low concentration of demecolcine, which partially depolymerises microtubles from mitotic spindles, approximately 50% of mars91 mutant embryos completely lose microtubules from around the chromosomes, while the remaining embryos exhibit much weaker staining of the microtubules. mars91 mutants are less resistant to demecolcine microtubule depolymerisation.
mars91 embryonic cells exhibit dissociation of centrosomes from mitotic spindles. The mitotic spindles without centrosomes tend to collapse into monopolar spindles.
90.8% of embryos from homozygous mars91 parents die during embryogenesis, with the majority of embryos displaying defects in cellularisation. 9.2% hatch into larvae, but only 5.5% of embryos survive to adulthood. Embryos from mars91 homozygous parents display severe mitotic defects during the rapid nuclear divisions in early syncytial blastoderm stage embryos. Centrosomes frequently detach from spindles and from the nuclear envelope and nucleate astral microtubules in ectopic positions.
mars91/Df(2R)CX1 animals are viable and fertile. Offspring of mars91/Df(2R)CX1 have severe embryonic defects and the majority die during embryogenesis.
mars91 is rescued by marsUASp.N.GFP
mars91 is rescued by marsUASp.EGFP/Scer\GAL4VP16.mat.αTub67C
mars91 is not rescued by Scer\GAL4da.G32/mars1-430.UASp.N.GFP
mars91 is not rescued by mars431-921.UASp.N.GFP
Expression of mars1-430.Scer\UAS.P\T.N.T:Avic\GFP fails to rescue the lethality associated with mars91 mutants but is able to largely maintain the mitotic spindle morphology in the absence of endogenous mars.
Expression of marsScer\UAS.P\T.T:Avic\GFP-EGFP under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16 fully rescues the embryogenesis defects in offspring from mars91 homozygous parents.