Amino acid replacement: A270V.
C16857226T
A270V | sina-PA; A270V | sina-PB; A270V | sina-PC
A270V
Site of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
sinaA4 homozygous and sinaA4/Df(3L)sinaSH transheterozygous females have meiotic defects, as shown by frequent X-chromosome and 4[[th]]-chromosome non-disjunction, which is associated with a severe decrease in X-chromosome crossover/recombination, but not with defects in double strand DNA break formation and repair during oogenesis. In agreement, prometaphase I/metaphase I oocytes show recombination-defective chromosome configurations (i.e. not aligned at the metaphase plate) that are not observed in controls.
sinaA4/Df(3L)sinaSH transheterozygotes exhibit defects in synaptonemal complex assembly during oogenesis: the complex assembles with relatively normal timing, exhibiting tracks in multiple nuclei in early pachytene (region 2A) o the germarium; as the cysts progress, however, the synaptonemal complex loses its curved, track-like pattern and instead its components form narrow rod-like polycomplexes; at early/mid-pachytene (germarium region 2B) the polycomplexes remain in a subset of nuclei that would have normally disassembled their synaptonemal complex to become nurse cells, but the oocyte is correctly specified, as cysts exhibit a single Orb-positive nucleus; polycomplexes persist in nurse cells during mid-prophase (stages 2-9), as well as in the oocyte during late prophase (stages 10-12) and pro-metaphase I/metaphase I (stage 13); while centrosomes can associate with polycomplexes, they fail to cluster into 1 or 2 foci; the polycomplexes that persisted into later stages in both the pro-oocyte and nurse cells frequently are associated with centromeres; small polycomplexes are also observed in the premeiotic region 1, where only foci of synaptonemal complex components are observed in wild type controls.
sinaA4 homozygotes exhibit defects in synaptonemal complex assembly during oogenesis: the complex assembles with relatively normal timing, exhibiting tracks in multiple nuclei in early pachytene (region 2A) o the germarium; as the cysts progress, however, the synaptonemal complex loses its curved, track-like pattern and instead its components form narrow rod-like polycomplexes; at early/mid-pachytene (germarium region 2B) the polycomplexes remain in a subset of nuclei that would have normally disassembled their synaptonemal complex to become nurse cells; however, the oocyte is correctly specified, as cysts exhibit a single Orb-positive nucleus. While centrosomes can associate with polycomplexes, they fail to cluster into 1 or 2 foci.
sina3/sinaA4 transheterozygotes also exhibit frequent X-chromosome and 4[[th]]-chromosome non-disjunction, as well as defects in synaptonemal complex assembly during oogenesis, with components forming abnormal polycomplexes, which remain in both oocytes and nurse cells by stage 2.
sinaA4 has female germline cyst | oogenesis phenotype, suppressible | partially by c(2)MEP2115/c(2)MEP2115
Df(3L)sinaSH, sinaA4 has female germline cyst | oogenesis stage S1 phenotype, suppressible | partially by c(2)MEP2115/c(2)MEP2115
sinaA4 has synaptonemal complex | oogenesis stage S1 phenotype, suppressible | partially by c(2)MEP2115/c(2)MEP2115
Df(3L)sinaSH, sinaA4 has synaptonemal complex | oogenesis phenotype, suppressible | partially by c(2)MEP2115/c(2)MEP2115