Survivin regulates chromosome segregation by modulating the phosphorylation of Aurora B during porcine oocyte meiosis

Cell Cycle. 2018;17(21-22):2436-2446. doi: 10.1080/15384101.2018.1542894. Epub 2018 Nov 14.

Abstract

SURVIVIN is an essential chromosomal passenger complex (CPC) subunit and participates in cell division. In this study, we used porcine oocyte as a model to investigate the roles of Survivin during porcine oocyte maturation. Survivin was highly expressed in germinal vesicle (GV) and germinal vesicle breakdown (GVBD) stages oocytes, mainly localized in the GV at GV stage and on the chromosomes after GVBD. We have used RNA interference to specifically deplete Survivin in oocytes during in vitro maturation (IVM). Immunofluorescence assay showed that Survivin-depleted oocytes failed to produce polar body in meiosisⅠ (failed to complete cytokinesis), and they were arrested in metaphaseⅠwith misaligned chromosomes. The homologous chromosomes in Survivin-depleted oocytes could not be separated normally. Moreover, both the phosphorylation levels of Aurora B and the mRNA level of Mad2L1 related to spindle assembly checkpoint (SAC) was decreased in Survivin-depleted oocytes, which thus inhibited the degradation of Cyclin B1 (CCNB1) to complete meiosis. Taken together, we conclude that Survivin is an important mediator of centromere and midbody docking of Aurora-B as well as its activity and regulates SAC and MPF activity during meiosis in porcine oocytes.

Keywords: Survivin; chromosomes; metaphase I; oocyte; pig; spindle assembly checkpoint.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aurora Kinase B / metabolism*
  • Cells, Cultured
  • Chromosome Segregation*
  • Female
  • Gene Expression Regulation, Developmental
  • Meiosis*
  • Oocytes / enzymology*
  • Phosphorylation
  • Signal Transduction
  • Spindle Apparatus / enzymology
  • Spindle Apparatus / genetics
  • Survivin / genetics
  • Survivin / metabolism*
  • Sus scrofa

Substances

  • Survivin
  • Aurora Kinase B

Grants and funding

This research was supported by the Natural Science Foundation of Hubei Province (Grant# 2018CFA015); National Key Research and Development Program of China; Stem Cell and Translational Research (Grant# 2016YFA0100203); National Project for Breeding of Transgenic Pig (2016ZX08006-002).