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Updated: Mar 29, 2026

Real-Time Monitoring of Aurora kinase A Activation using Conformational FRET Biosensors in Live Cells
Published on: July 30, 2020
The Dawn of Aurora Kinase Research: From Fly Genetics to the Clinic
Mar Carmena1, William C Earnshaw1, David M Glover2
1Wellcome Trust Centre for Cell Biology, The University of Edinburgh Edinburgh, UK.
Abstract:
Aurora kinases comprise a family of highly conserved serine-threonine protein kinases that play a pivotal role in the regulation of cell cycle. Aurora kinases are not only involved in the control of multiple processes during cell division but also coordinate chromosomal and cytoskeletal events, contributing to the regulation of checkpoints and ensuring the smooth progression of the cell cycle. Because of their fundamental contribution to cell cycle regulation, Aurora kinases were originally identified in independent genetic screens designed to find genes involved in the regulation of cell division. The first aurora mutant was part of a collection of mutants isolated in C. Nusslein-Volhard's laboratory. This collection was screened in D. M. Glover's laboratory in search for mutations disrupting the centrosome cycle in embryos derived from homozygous mutant mothers. The mutants identified were given names related to the "polar regions," and included not only aurora but also the equally famous polo. Ipl1, the only Aurora in yeast, was identified in a genetic screen looking for mutations that caused chromosome segregation defects. The discovery of a second Aurora-like kinase in mammals opened a new chapter in the research of Aurora kinases. The rat kinase AIM was found to be highly homologous to the fly and yeast proteins, but localized at the midzone and midbody and was proposed to have a role in cytokinesis. Homologs of the equatorial Aurora (Aurora B) were identified in metazoans ranging from flies to humans. Xenopus Aurora B was found to be in a complex with the chromosomal passenger INCENP, and both proteins were shown to be essential in flies for chromosome structure, segregation, central spindle formation and cytokinesis. Fifteen years on, Aurora kinase research is an active field of research. After the successful introduction of the first anti-mitotic agents in cancer therapy, both Auroras have become the focus of attention as targets for the development of new anti-cancer drugs. In this review we will aim to give a historical overview of the research on Aurora kinases, highlighting the most relevant milestones in the advance of the field.
Insights
Aurora kinases are crucial serine-threonine protein kinases regulating cell division. Their pivotal role in cell cycle control makes them key targets for novel anti-cancer drug development.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Aurora kinases are highly conserved serine-threonine protein kinases essential for cell cycle regulation.
- They coordinate chromosomal and cytoskeletal events, ensuring proper cell division progression and checkpoint control.
Purpose of the Study:
- To provide a historical overview of Aurora kinase research.
- To highlight key milestones in understanding their function and therapeutic potential.
Main Methods:
- Review of genetic screens for cell division regulators.
- Identification and characterization of Aurora kinase homologs across species.
- Analysis of Aurora kinase involvement in cell cycle processes.
Main Results:
- Discovery of Aurora kinases through genetic screens in yeast and flies.
- Identification of mammalian homologs (e.g., Aurora B) involved in cytokinesis.
- Demonstration of Aurora B's essential role in chromosome segregation and spindle formation.
Conclusions:
- Aurora kinases are fundamental to cell cycle progression and mitosis.
- Their critical roles establish them as significant targets for anti-cancer therapies.
- Ongoing research continues to advance the understanding and therapeutic application of Aurora kinases.

