Cyclin B1 is essential for mitosis in mouse embryos, and its nuclear export sets the time for mitosis

J Cell Biol. 2018 Jan 2;217(1):179-193. doi: 10.1083/jcb.201612147. Epub 2017 Oct 26.

Abstract

There is remarkable redundancy between the Cyclin-Cdk complexes that comprise the cell cycle machinery. None of the mammalian A-, D-, or E-type cyclins are required in development until implantation, and only Cdk1 is essential for early cell divisions. Cyclin B1 is essential for development, but whether it is required for cell division is contentious. Here, we used a novel imaging approach to analyze Cyclin B1-null embryos from fertilization onward. We show that Cyclin B1-/- embryos arrest in G2 phase after just two divisions. This is the earliest arrest of any Cyclin known and places Cyclin B1 with cdk1 as the essential regulators of the cell cycle. We reintroduced mutant proteins into this genetically null background to determine why Cyclin B1 is constantly exported from the nucleus. We found that Cyclin B1 must be exported from the nucleus for the cell to prevent premature entry to mitosis, and retaining Cyclin B1-Cdk1 at the plasma membrane precludes entry to mitosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus / physiology
  • Animals
  • CDC2 Protein Kinase / genetics*
  • Cell Cycle Proteins / metabolism
  • Cyclin B1 / genetics*
  • DNA-Binding Proteins / metabolism
  • Embryonic Development / genetics*
  • Mice
  • Mice, Knockout
  • Mitosis / genetics*
  • Nuclear Proteins / metabolism
  • Phosphorylation
  • Protein-Tyrosine Kinases / metabolism
  • Transcription Factors / metabolism
  • cdc25 Phosphatases / metabolism

Substances

  • Ccnb1 protein, mouse
  • Cell Cycle Proteins
  • Cyclin B1
  • DNA-Binding Proteins
  • Myt1 protein, mouse
  • Nuclear Proteins
  • Transcription Factors
  • Protein-Tyrosine Kinases
  • Wee1 protein, mouse
  • CDC2 Protein Kinase
  • Cdk1 protein, mouse
  • Cdc25a protein, mouse
  • cdc25 Phosphatases