Active Cells, Biochemistry & Physiology Genetics & Molecular Biology

The Principles of Centriole and Centrosome Biogenesis

In plain English

AI plain-English summary

Every human cell is born with a single centrosome—a tiny protein machine that orchestrates cell division and organisation—and cells can assemble a new one from hundreds of parts in minutes, with near-perfect precision. Yet scientists do not understand how cells achieve this feat. When centrosomes go wrong, the consequences range from cancer to diabetes to microcephaly and dwarfism. This project aims to crack the molecular rules that govern centrosome assembly. The researchers will build a near-complete mathematical model of the process and, separately, reconstitute centrosome assembly on the surface of synthetic structures. If successful, this work will reveal the fundamental principles by which a complex organelle builds itself with such spatial and temporal accuracy. This is fundamentally curiosity-driven science. There is no immediate practical application. But a deep understanding of how cells assemble intricate protein machines could, in the longer term, guide the design of human-made biological nanomachines—tiny devices that might one day perform tasks inside the body or in industrial processes, much as past fundamental research on molecular motors and self-assembly laid the groundwork for today’s synthetic biology.

View original technical description
Almost every cell in the human body is born with a single centrosome. These organelles play an important part in many aspects of cell organisation, and their dysfunction has been linked to a plethora of human pathologies, ranging from cancer to diabetes to microcephaly and dwarfism. Centrosomes are composed of many hundreds of proteins, yet some cells can precisely assemble new centrosomes in just a few minutes, nearly always forming the right number of centrosomes in the right place, at the right time, and growing each centrosome to the right size. Our overarching goal is to understand the molecular mechanisms that allow cells to build such complicated protein machines with such remarkable spatial and temporal precision. We will approach this in two ways: (1) We will generate datasets to construct a near-complete mathematical model of centrosome assembly; (2) We will reconstitute centrosome assembly on the surface of synthetic structures. Together, these approaches will provide both an unparalleled understanding of the principles that govern the biogenesis of a complex organelle, and a conceptual framework with which to probe organelle biogenesis more generally. In the future, these principles may help guide the production of similarly complex human-designed biological nanomachines.

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Researchers

Jordan Raff (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Structural mechanisms of centriole assembly during cell duplication
Centriole and centrosome assembly
Decoding the regulatory mechanisms that govern centriole distal end function in health and disease
Three dimensional organisation and duplication of the eukaryotic basal body
Deciphering the molecular dynamics of centriole and centrosome biogenesis

Original classification

Discovery Award

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