Amino acid replacement: Q858term.
C8567022T
Q858term | Cenp-C-PA; Q846term | Cenp-C-PB
Q858term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Cenp-CZ3-4375/Cenp-CIR35 females show defects in centromere clustering in the oocyte, with a failure of clustering being evidence by pachytene in region 3 of the germarium (centromere clustering at the earlier zygotene stage is normal). Defects in centromere pairing are also seen.
The centromeres are separated from the nucleolus in the oocytes of Cenp-CZ3-4375/Cenp-CIR35 females (in contrast to wild type where they are adjacent).
Heterozygous females show significantly increased X chromosome nondisjunction compared to wild-type controls. The nondisjunction events occur in meiosis I.
Mutants show cell cycle defects during embryogenesis.
Cenp-CIR35 has abnormal meiotic cell cycle | semidominant phenotype, enhanceable by cal12k32/cal1[+]
Cenp-C[+]/Cenp-CIR35 is an enhancer of abnormal meiotic cell cycle | semidominant phenotype of cal12k32
Cenp-CIR35 is an enhancer of visible phenotype of Scer\GAL4GMR.PF, pimUAS.Tag:MYC
Cenp-C[+]/Cenp-CIR35 is an enhancer of visible phenotype of Scer\GAL4GMR.PF, cidUAS.cJa
Cenp-CIR35 is an enhancer of eye phenotype of Scer\GAL4GMR.PF, pimUAS.Tag:MYC
Cenp-C[+]/Cenp-CIR35 is an enhancer of eye phenotype of Scer\GAL4GMR.PF, cidUAS.cJa
Cenp-CIR35, Df(3R)Exel6176/+ has oocyte phenotype
Cenp-CIR35, Df(3R)Exel6176/+ has chromosome, centromeric region phenotype
Cenp-CIR35, cal12k32/cal1[+] has chromosome, centromeric region phenotype
Cenp-C[+]/Cenp-CIR35, cal12k32 has oocyte phenotype
Cenp-C[+]/Cenp-CIR35, cal12k32 has chromosome, centromeric region phenotype
Cenp-CIR35/Df(3R)Exel6176 double heterozygous females do not show a significant increase in X chromosome non disjunction compared to wild-type controls.
cal12k32/Cenp-CIR35 and Df(3R)Exel6176/Cenp-CIR35 double heterozygous females show defects in centromere clustering in the oocyte, with defects being evident by region 3 of the germarium. Defects in centromere pairing are also seen.
The centromeres are separated from the nucleolus in the oocytes of double heterozygous cal12k32/Cenp-CIR35 females (in contrast to wild type where they are adjacent).
cal12k32/Cenp-CIR35 double heterozygous females show significantly increased X and 4th chromosome nondisjunction compared to wild-type controls, with the frequency of nondisjunction being increased compared to the phenotypes seen in single heterozygotes.
Cenp-CIR35/Cenp-CZ3-4375 is rescued by Cenp-CEYFP
Cenp-CT:Avic\GFP-EYFP restores normal centromere clustering in the oocytes of Cenp-CZ3-4375/Cenp-CIR35 females.
K. Dej T. Orr-Weaver