Active Cells, Biochemistry & Physiology Genetics & Molecular Biology

How does the cell assemble the mitotic trigger?

In plain English

AI plain-English summary

Every time a human cell divides, it must first assemble a molecular switch—a protein complex called cyclin B1/Cdk1—that flips to trigger the entire process. Without this switch, division never starts. Despite decades of study, scientists have not understood exactly how cells build this trigger. Traditional biochemical methods could not capture the fleeting, step-by-step assembly of the complex inside living cells. The researchers now plan to use gene editing, advanced imaging, and proteomics to watch these steps in real time. They will focus on two unresolved questions: how cyclin B1 and Cdk1 first bind together, and how the activated complex then rushes into the cell’s nucleus to start division. This is fundamental science. It will not produce a drug or a diagnostic tool tomorrow. But cell division sits at the heart of development, tissue repair, and cancer—where the trigger gets stuck in the “on” position. Understanding how the cell assembles its mitotic switch could, in the longer term, reveal new points of vulnerability in cancer cells or explain how tissues shape themselves during embryonic growth. Past work on cell cycle mechanics has already led to cancer therapies; this project digs deeper into the machinery itself.

View original technical description
Cyclin B1/Cdk1 is both the regulatory hub and the trigger for cell division. Despite this crucial role, key aspects of cyclin B1/Cdk1 regulation have remained elusive due to the limitations of traditional biochemical studies. Recent technical advances mean we are now able to address these long-standing questions, and our work has revealed unsuspected regulatory steps in how the cell assembles the machinery to trigger mitosis. Here, we propose to apply gene editing, advanced cell imaging and proteomics to further our understanding of how the cell assembles the mitotic trigger, specifically: the regulation of cyclin B1-Cdk1 binding; and the how activating cyclin B1/Cdk1 moves it rapidly into the nucleus. The insights gained from this research will deepen our understanding of cell cycle mechanics and provide important implications for tissue morphogenesis and cancer biology.

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Researchers

Jonathon Pines (Principal Investigator)

Related Research

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CDK-containing macromolecular assemblies

Original classification

Research and Innovation

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