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Cyclin B2 can compensate for Cyclin B1 in oocyte meiosis I.

Jian LiJi-Xin TangJin-Mei ChengBian HuYu-Qian WangBatool AaliaXiao-Yu LiCheng JinXiu-Xia WangShou-Long DengYan ZhangSu-Ren ChenWei-Ping QianQing-Yuan SunXing-Xu HuangYi-Xun Liu
Published in: The Journal of cell biology (2018)
Mammalian oocytes are arrested at the prophase of the first meiotic division for months and even years, depending on species. Meiotic resumption of fully grown oocytes requires activation of M-phase-promoting factor (MPF), which is composed of Cyclin B1 and cyclin-dependent kinase 1 (CDK1). It has long been believed that Cyclin B1 synthesis/accumulation and its interaction with CDK1 is a prerequisite for MPF activation in oocytes. In this study, we revealed that oocyte meiotic resumption occurred in the absence of Cyclin B1. Ccnb1-null oocytes resumed meiosis and extruded the first polar body. Without Cyclin B1, CDK1 could be activated by up-regulated Cyclin B2. Ccnb1 and Ccnb2 double knockout permanently arrested the oocytes at the prophase of the first meiotic division. Oocyte-specific Ccnb1-null female mice were infertile due to failed MPF activity elevation and thus premature interphase-like stage entry in the second meiotic division. These results have revealed a hidden compensatory mechanism between Cyclin B1 and Cyclin B2 in regulating MPF and oocyte meiotic resumption.
Keyphrases
  • cell cycle
  • cell proliferation
  • cell cycle arrest
  • cell death
  • type diabetes
  • skeletal muscle
  • metabolic syndrome
  • signaling pathway
  • transcription factor
  • pi k akt
  • tyrosine kinase
  • high fat diet induced