Amino acid replacement: P1115S.
C8567865T
P1116S | Cenp-C-PA; P1104S | Cenp-C-PB
P1115S
Reported as a P1115S mutation relative to Cenp-C-PA. 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 evident by pachytene in region 3 of the germarium (centromere clustering at the earlier zygotene stage is normal). Defects in clustering are also seen in the oocytes of homozygous Cenp-CZ3-4375 females, although they are not as pronounced as those seen in the transheterozygous Cenp-CZ3-4375/Cenp-CIR35 females. Defects in centromere pairing are also seen, in the oocytes of both homozygous Cenp-CZ3-4375 and transheterozygous Cenp-CZ3-4375/Cenp-CIR35 females.
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).
Cenp-C[+]/Cenp-CZ3-4375, cal12k32 has oocyte phenotype
Cenp-C[+]/Cenp-CZ3-4375, cal12k32 has chromosome, centromeric region phenotype
cal12k32/Cenp-CZ3-4375 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.
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.