Amino acid replacement: ?592term.
Amino acid replacement: Q592term.
C15377394T
Q592term | dup-PA; Q592term | dup-PB
Q592term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
mitosis & nuclear chromosome
Homozygous embryos show weak BrdU incorporation during a prolonged and partial S phase of cycle 16.
Cells in homozygous dupa1 mutant embryos enter mitosis 16 (M16) later than heterozygous controls. A partial S phase 16 is also seen. Once in M16 the cells are arrested remain in this state until at least stage 13, and mitotic cells are still visible at stage 15. Spindles in these mutants contain apparently functional centrosomes, chromosomes fail to align properly. Most chromosomes lie within the bipolar spindle but are scattered and not compacted into a metaphase plate. Severe alignment defects are seen in about 80% of mitotic cells.
dupa3 has abnormal mitotic cell cycle phenotype, suppressible by BubR1k03113
dupa3 has abnormal mitotic cell cycle phenotype, suppressible by mei-41D3
dupa3 has mitotic cell cycle phenotype, suppressible by BubR1k03113
dupa3 has mitotic cell cycle phenotype, suppressible by mei-41D3
In dupa3, mei-41D3 double mutants the mitosis 16 (M16) entry delay phenotype is absent. The addition of Bub1k03113 to dupa3 mutants suppresses the M16 arrest phenotype.
In dupa3, mei-41D3 double mutants the mitosis 16 (M16) entry delay phenotype is absent.
The addition of BubR1k03113 to dupa3 mutants suppresses the M16 arrest phenotype.
dupa3 fails to complement dupl5.