In a remarkable breakthrough that challenges long-standing paradigms in cell biology, researchers at the Ruđer Bošković Institute (RBI) in Zagreb, Croatia, have revealed a transformative understanding of chromosome movement during cell division. For over two decades, the protein CENP-E was widely regarded as a motor protein—a biological engine hauling chromosomes to their designated positions within dividing cells. However, new rigorous studies led by Dr. Kruno Vukušić and Professor Iva Tolić demonstrate that CENP-E does not function as a force generator but instead plays a critical regulatory role facilitating the initial stabilization of chromosome attachments. This nuanced discovery rewrites the textbook narrative, providing a deeper insight into the exquisite orchestration required for accurate chromosome segregation and highlighting potential avenues for combating diverse diseases including cancer.
The process of mitosis—the accurate division of a single cell’s genetic material into two daughter cells—is one of biology’s most fundamental yet delicate operations. Each human cell must faithfully copy and distribute roughly three billion base pairs of DNA, ensuring complete and error-free inheritance. Missteps in this process have immediate and often devastating consequences, ranging from developmental abnormalities and infertility to the unchecked cellular proliferation characteristic of cancer. One of the most pivotal moments in mitosis occurs during metaphase, where chromosomes must align precisely at the spindle equator before being pulled apart. This alignment, known as chromosome congression, depends on intimate interactions between chromosomes and a dynamic cellular scaffold of microtubules.
For years, CENP-E was depicted as a motor protein physically transporting chromosomes along microtubule tracks to the center of the cell, effectively a biological locomotive dragging cargo to the metaphase plate. The elegant simplicity of this model aligned nicely with known motor proteins’ functions elsewhere in cells, but it failed to fully explain observed behaviors under more nuanced experimental scrutiny. The work emerging from the team in Zagreb instead portrays CENP-E as a sophisticated regulator that stabilizes the initial “end-on” attachments between chromosomes and spindle microtubules. Rather than pulling chromosomes themselves, CENP-E ensures the attachments are robust enough for successful congression to proceed. Without these secure initial contacts, chromosomes hesitate or stall, leaving the entire mitotic process susceptible to catastrophic errors.
To understand this role, it is instructive to envision the cell as a bustling urban traffic network, where chromosomes resemble trains trying to reach a central station via rails formed by microtubules. In this analogy, the old model imagined CENP-E as a powerful locomotive engine towing the trains. The new findings from RBI reveal that CENP-E acts less like an engine and more like an essential coupling mechanism—ensuring that each train securely hitches onto its railcar before departure. Chromosomes that fail to form stable attachments cannot advance, akin to trains stalled at station outskirts unable to proceed to their destination. This shift from imagining CENP-E as a driver to a critical stabilizer reframes our understanding of mitotic mechanics at the molecular level.
Crucially, this regulatory function of CENP-E operates in tandem with a family of proteins known as Aurora kinases, which function analogously to cellular traffic lights controlling the timing and placement of chromosome attachments. Aurora kinases emit “red light” signals that destabilize premature or misplaced connections, preventing chromosomes from anchoring at inappropriate spindle regions near the cell poles. This safety mechanism, while vital, risks over-inhibition, stalling chromosomes in suboptimal locations. CENP-E counterbalances this by modulating the signaling environment—effectively reducing the “red light” intensity just enough to permit chromosomes to establish the necessary end-on attachments. Thus, the interplay between CENP-E and Aurora kinases ensures the fidelity of chromosome alignment without compromising the safeguards that prevent errors.
From a mechanistic perspective, CENP-E’s action involves finely tuned molecular interactions at the kinetochore—the protein complex where chromosomes interface with microtubules. This stabilization initiates proper biorientation, a state where sister chromatids are attached to opposite spindle poles, generating tension essential for checkpoint satisfaction and progression to anaphase. Before this study, it was unclear whether CENP-E contributed mechanical force or regulatory modulation at this juncture. The Zagreb research definitively uncouples CENP-E’s role from cargo transport, positioning it as a molecular switch that enables the progression of congression by stabilizing kinetochore-microtubule attachments.
These groundbreaking findings not only dismantle a two-decade-old dogma but also illuminate critical vulnerabilities in the mitotic machinery relevant to disease. Aberrant chromosome segregation is a hallmark of many cancer types, where genomic instability leads to the characteristic patchwork of chromosomal gains and losses. By elucidating the precise molecular function of CENP-E in opposition to Aurora kinases, the researchers have identified a delicate balance that could be therapeutically exploited. Drugs fine-tuning this regulatory equilibrium may suppress uncontrolled mitotic progressions or rescue cells with stalled division, offering novel avenues for cancer treatment and improved diagnostics.
The research’s scientific impact is amplified by its methodological innovation and collaborative scope. Leveraging state-of-the-art imaging techniques that color-code microtubule architecture by depth, and deploying powerful computational modeling at the University of Zagreb’s SRCE center, the team integrated empirical data with predictive simulations. This interdisciplinary approach illustrates the modern paradigm in cell biology, where molecular detail converges with computational rigor to reveal complex cellular behaviors once obscured in noise. This synergy of experimental and theoretical frameworks is epitomized in the leadership of Dr. Kruno Vukušić—a rising star preparing to establish his own research group—and Professor Iva Tolić, an internationally recognized cell biophysicist supported by multiple European Research Council grants.
Beyond the immediate mechanistic revelations, this study challenges how biological education frames mitotic processes, pushing away from simplified mechanical analogies towards appreciating timing, regulation, and molecular crosstalk. It underscores an essential truth in biology: apparent chaos at the cellular level is governed by intricate, finely balanced systems adapted over eons to navigate the constraints of physical law and biological necessity. By redefining CENP-E’s role within this context, the Zagreb researchers have provided a clearer blueprint for how cells maintain genomic integrity under immense systemic pressure.
This discovery also highlights the importance of global collaboration and investment in scientific infrastructure. Supported by one of the most competitive European grants—the ERC Synergy Award—alongside contributions from national science foundations and bilateral international projects, this research underscores Europe’s leading role in advancing frontiers of cellular biology. It demonstrates how pooled resources, combined expertise, and cutting-edge computational infrastructure can yield insights that none could achieve in isolation. As Prof. Tolić stresses, modern biology transcends traditional lab work; it thrives on computation, integration, and cross-border collaboration.
Ultimately, the findings from Zagreb represent a paradigm shift with broad ramifications extending from fundamental biology to clinical applications. By uncovering the interplay between CENP-E and Aurora kinases in stabilizing chromosome attachments—the very first step in the meticulous dance of mitosis—this work advances an understanding of cellular fidelity that moves us closer to deciphering and potentially correcting the molecular underpinnings of diseases rooted in chromosome instability.
The work punctuates the extraordinary elegance and precision of molecular choreography culminating in each cell division, reminding us that life’s continuity hinges on more than mechanical force: it depends on finely tuned regulatory networks that control timing, attachment, and coordination. As research builds on these insights, new therapies designed to modulate these networks may emerge, offering hope for treating genetic disorders and cancers with unprecedented precision and efficacy.
Subject of Research: Cells
Article Title: CENP-E initiates chromosome congression by opposing Aurora kinases to promote end-on attachments
News Publication Date: 21-Oct-2025
Web References: https://doi.org/10.1038/s41467-025-64148-w
Image Credits: Kruno Vukušić, Tolić lab, Ruđer Bošković Institute
Keywords: CENP-E, chromosome congression, Aurora kinases, mitosis, kinetochore-microtubule attachment, cell division, chromosome segregation, cancer, genomic instability, cell biology, molecular regulation, microtubules, cell biophysics
Tags: accurate chromosome segregationcell biology breakthroughscell division mechanismsCENP-E protein functionchallenges in cell division modelschromosome attachment stabilizationchromosome movement regulationgenetic material distributionimplications for disease treatmentmitosis and cancer connectionresearch at Ruđer Bošković Instituteunderstanding cellular processes
