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Related Concept Videos

Negative Regulator Molecules01:23

Negative Regulator Molecules

Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
M-Cdk Drives Transition Into Mitosis02:15

M-Cdk Drives Transition Into Mitosis

Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
The Cell Cycle Control System01:28

The Cell Cycle Control System

The cell cycle regulation directs how a cell proceeds from one phase to the next and begins mitosis. The cell cycle control system includes intracellular regulatory molecules and external triggers. They provide "stop" or "advance" signals and operate at specific cell cycle stages termed checkpoints to ensure that a particular process is completed before the cell advances to the next phase.
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Molecular Factors Affecting Cell Division

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Related Experiment Video

Updated: Jul 25, 2026

Methods for Precisely Localized Transfer of Cells or DNA into Early Postimplantation Mouse Embryos
09:04

Methods for Precisely Localized Transfer of Cells or DNA into Early Postimplantation Mouse Embryos

Published on: December 25, 2015

Cell cycle regulation in early mouse embryos.

J Z Kubiak1, M A Ciemerych

  • 1CNRS UMR 6061, University of Rennes 1, Faculty of Medicine, 2 Ave Prof Leon Bernard, CS 34317, 35043 Rennes, France.

Novartis Foundation Symposium
|July 11, 2001
PubMed
Summary

Early mouse embryo cell cycles differ from somatic cells, particularly in meiosis-to-mitosis transition and M phase regulation. These findings impact understanding of cell cycle control and early development.

Area of Science:

  • Developmental Biology
  • Cell Cycle Research
  • Embryology

Background:

  • Classical view: early mouse embryo cell cycles mirror somatic cell cycles.
  • Observation: earliest mitotic divisions suggest significant embryonic differences.
  • Significance: understanding differences impacts general cell cycle mechanisms and embryo development.

Purpose of the Study:

  • Describe differences in the first two cell cycles of the mouse embryo.
  • Investigate the transition from meiotic to mitotic cell cycle.
  • Analyze regulation of mitotic entry and duration in early embryonic divisions.

Main Methods:

  • Studied mouse oocyte activation and cell cycle transition.
  • Examined nucleus-independent activation of M phase-promoting factor (MPF).

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Single-Cell RNA Sequencing of Mutant Whole Mouse Embryos: From the Epiblast to the End of Gastrulation

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09:14

Single-Cell RNA Sequencing of Mutant Whole Mouse Embryos: From the Epiblast to the End of Gastrulation

Published on: June 14, 2024

  • Analyzed regulation of early embryonic mitosis duration.
  • Main Results:

    • Mouse oocytes inactivate cytostatic factor (CSF) to switch from meiotic to mitotic cycles.
    • M phase-promoting factor (MPF) activation is nucleus-independent for mitotic entry.
    • Developmentally regulated phenomena are integrated with cell cycle machinery during early mitoses.

    Conclusions:

    • Early mouse embryonic cell cycles exhibit unique features distinct from somatic cells.
    • The transition from meiosis to mitosis is a key developmental event.
    • Cell cycle regulation in early embryos is tightly coordinated with developmental processes.