polo16-1/polo[+] is an enhancer of abnormal mitotic cell cycle phenotype of sub131/sub1
polo16-1/polo[+] is a suppressor of abnormal meiotic cell cycle | dominant phenotype of mtrm126
polo16-1, sub131/sub1 has decreased body size | adult stage phenotype
polo16-1/polo[+], sub131/sub1 has lethal | larval stage phenotype
polo16-1/polo[+] is an enhancer of brain | larval stage phenotype of sub131/sub1
polo16-1/polo[+] is a suppressor | partially of oocyte nucleus | oogenesis stage S12 phenotype of mtrm126
poloKG03033/+ suppresses the elevated levels of achiasmate X and 4th chromosome nondisjunction seen in In(1)FM7/X mtrm126/+ females.
The precocious nuclear envelope breakdown (NEB) seen in stage 12 oocytes of mtrm126/+ females is strongly suppressed by polo16-1/+. The defects in karyosome morphology seen in mtrm126/+ oocytes observed within 20 minutes of NEB are also largely suppressed by polo16-1/+.
polo16-1/+ largely suppresses the karyosome maintenance defects seen in mtrm126/+ oocytes. polo16-1/+ fully suppresses the defect in X and 4th chromosome centromere co-orientation that is seen in mtrm126/+ females.
sub1/sub131; polo16-1/+ rare survivors are sickly and small with abdominal patterning defects. Late larval developmental arrest is observed. Severe defects in spindle organization are observed, and spindles are unusually short. Larvae show a higher percentage of cells in mitosis compared to sub1/sub131 or polo16-1/+, and nearly four times that of wild-type.
polo16-1/Df(3L)rdgC-co2 is partially rescued by polowt.GFP
polo16-1/Df(3L)rdgC-co2 is not rescued by poloH518A.K520M.GFP
polowt.T:Avic\GFP rescues the lethality of polo16-1/Df(3L)rdgC-co2 animals, but rescued females are sterile.
poloH518A.K520M.T:Avic\GFP fails to rescue the lethality of polo16-1/Df(3L)rdgC-co2 animals.