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Multiple pools of PP2A regulate spindle assembly, kinetochore attachments and cohesion in Drosophila oocytes
Author(s) -
Janet K. Jang,
Amy C. Gladstein,
Arunika Das,
Joanatta G. Shapiro,
Zachary Sisco,
Kim S. McKim
Publication year - 2021
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.254037
Subject(s) - biology , kinetochore , microbiology and biotechnology , meiosis , meiosis ii , spindle apparatus , anaphase , chromosome segregation , aurora b kinase , protein phosphatase 2 , establishment of sister chromatid cohesion , oocyte , genetics , cohesin , cell division , chromosome , phosphatase , embryo , phosphorylation , gene , cell
Meiosis in female oocytes lacks centrosomes, the microtubule-organizing centers. In Drosophila oocytes, meiotic spindle assembly depends on the chromosomal passenger complex (CPC). To investigate the mechanisms that regulate Aurora B activity, we examined the role of protein phosphatase 2A (PP2A) in Drosophila oocyte meiosis. We found that both forms of PP2A, B55 and B56, antagonize the Aurora B spindle assembly function, suggesting that a balance between Aurora B and PP2A activity maintains the oocyte spindle during meiosis I. PP2A-B56, which has a B subunit encoded by two partially redundant paralogs, wdb and wrd, is also required for maintenance of sister chromatid cohesion, establishment of end-on microtubule attachments, and metaphase I arrest in oocytes. WDB recruitment to the centromeres depends on BUBR1, MEI-S332 and kinetochore protein SPC105R. Although BUBR1 stabilizes microtubule attachments in Drosophila oocytes, it is not required for cohesion maintenance during meiosis I. We propose at least three populations of PP2A-B56 regulate meiosis, two of which depend on SPC105R and a third that is associated with the spindle.

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