Only two days to go until the “Mitotic Spindle: From Living and Synthetic Systems to Theory” meeting in Dubrovnik! This is the 4th time Nenad Pavin and I are organizing it, and it keeps growing with each edition. Can’t wait to see everyone in Dubrovnik! shorturl.at/35Vff
Gerben Vader
@vaderlab.bsky.social
Cell biologist/Geneticist. Princess Maxima Center for Pediatric Oncology - Utrecht, the Netherlands Investigating the molecular adaptations that drive meiosis, and how meiotic factors are hijacked by cancer cells.
Excited to share our structural insights into how microtubules differentially guide phosphorylation of kinetochore-microtubule regulators, Ndc80 and MCAK, for chromosome segregation. Heroic efforts by Yiming Niu with a fun collaboration with Jennifer DeLuca lab! www.science.org/doi/10.1126/...
Microtubules guide Aurora B substrate geometries for accurate chromosome segregation
Cryo-EM reveals how kinetochore-microtubule attachment is regulated by Aurora B substrate accessibility on microtubules.
science.org
Microtubules have been viewed as passive structural supports, but a study from @hirofunabiki.bsky.social in @science.org Advances redefines microtubules as active regulators, helping to prevent abnormalities in the number of chromosomes, a hallmark of cancer. 🔗: https://bit.ly/4v8miCC
Chromosomes stuck behind the spindle are ticking time bombs for aneuploidy. We uncovered a mechanical rescue mechanism where microtubule pivoting repositions these high-risk chromosomes! Out last week in @natcomms.nature.com, here's a thread 🧵 shorturl.at/OD89x
The newly established NeCEN Utrecht is looking for a #cryoEM scientist! www.uu.nl/en/organisat... Work with a new Krios 5 + pFIB and support cutting-edge life science research. 📍 Utrecht | 🗓 Apply by 30 April Please share with your network!
Cryo-electron microscopy scientist
Join our team to contribute to the operation and innovation of state-of-the-art cryo-electron microscopes and empower groundbreaking research.
uu.nl
Join us at the @themaximacenter.bsky.social! werkenbijprinsesmaximacentrum.nl/en/vacancy/j...
Junior Group Leader (Tenure Track) - Werken bij Prinses Maxima Centrum
The position You will be responsible for establishing and leading your own research group. As a junior group leader you are expected to establish a unique and impactful line of research funded through...
werkenbijprinsesmaximacentrum.nl
Mitosis lovers, get ready for Dubrovnik! 🔬🎉 I’m super excited to be organizing the 4th Mitotic Spindle Conference with Nenad Pavin, and we can’t wait to see you there! Want your abstract to be selected for a talk? Submit by Feb 8! www.phy.pmf.unizg.hr/~mitosis/ #SpindleCroatia2026
Mitosis has a timing system. If chromosomes attach properly, cells divide on schedule and keep proliferating. If attachment is slow or incomplete, the delay is recorded — and daughter cells stop dividing. We explore this link in our new preprint. 🔗 www.biorxiv.org/content/10.6...
Arianna Esposito Verza, @andrea-musacchio.bsky.social et al describe the long-sought-after mechanism of Bora dependency of PLK1 activation by Aurora A kinase during mitotic entry Another #RefereedPreprint ℅ @reviewcommons.org link.springer.com/article/10.1...
Molecular requirements for PLK1 activation by T-loop phosphorylation - The EMBO Journal
Activation of PLK1, a master mitotic kinase, requires phosphorylation of its activation segment on Thr210, within a basic consensus sequence for Aurora kinases. Aurora B-dependent phosphorylation of T...
link.springer.com
Registration is still open for this great meeting! Sign up for the 32nd ‘Dutch Cancer Biology Meeting’, focussed on the biology of cancer, which will be organized on March 5-6, 2026 in Lunteren, NL Registration: lnkd.in/ehKXDtpP More info: www.dutchcancerbiology.nl @marcelvanvugt.bsky.social
Dutch Cancer Biology Meeting | Cancer
Dutch Cancer Biology Meeting: a yearly two-day conference on the biology and genetics of cancer at Hotel de Werelt in Lunteren
dutchcancerbiology.nl
Join us in Lunteren, the Netherlands on March 5 & 6, 2026 for the 32nd Dutch Cancer Biology meeting. We have two fantastic keynote speakers: @andrea-musacchio.bsky.social and @colindascheele.bsky.social and the rest of the program will be by early-career scientists. Info: www.dutchcancerbiology.nl
All living organisms face the problem of parasites - but what happens when DNA has invaded the genome? go.nature.com/3MDiJCq
SOS: RNA-processing mechanism rescues genes from invasive DNA
Transposable elements can insert into genes, disrupting protein-coding potential. Researchers discover a mode of RNA processing, ‘SOS splicing’, that provides a quick fix.
go.nature.com
2 recent preprints show the mitotic stopwatch monitors more than just mitotic delays - it protects against WGD, cell enlargement and other stresses that mildly activate p53. It may act to amplify p53 signals to suppress tumourigenesis www.biorxiv.org/content/10.1... www.biorxiv.org/content/10.6...
The mitotic stopwatch limits the proliferation of whole genome doubled cells
Whole genome doubling (WGD) is a frequent event in tumourigenesis that promotes chromosomal instability and tumour evolution. WGD is sensed indirectly due to the presence of extra centrosomes, which a...
biorxiv.org
So proud to watch Jana turn a side quest into an entire research programme. Couldn’t imagine a more well-deserved outcome. 😍 The mighty yeast reveals what we believe are general principles of centromere evolution! Behind the curtain: communities.springernature.com/posts/counti... #MEvoSky 🧪🌎
Counting Chromosomes: The Simple Idea That Unlocked the Rules Behind Centromere Evolution
communities.springernature.com
How do new centromeres evolve while staying compatible with the division machinery? Discover it in our new Nature paper! We show centromeres transition gradually via a mix of drift, selection, and sex, reaching new states that still work with the kinetochore. 👉 doi.org/10.1038/s41586-025-09779-1
Why IDPs Are Poor Candidates for Homotypic LLPS 🧵👇A thread
Registration is open!🧬 Join us at Egmond aan Zee (April 19–24, 2026) for the next DNA Repair Meeting. We have an amazing line-up of speakers. 📅 Deadline for early registration: Jan 10, 2026 🔗 dnarepairmeeting-egmond2026.com
They did a great job of validating endogenous repair was not affected. The FRAP data indicates a high on/off rate at damage sites, which is what you probably need to prevent blocking other chromatin readers and repair proteins from accessing the damaged DNA.
Check out this beautiful paper by @richardcsilva.bsky.social et al., out now in @natcomms.nature.com. Great new DSB sensors to track DNA break formation and repair in real-time www.nature.com/articles/s41...
Engineered chromatin readers track damaged chromatin dynamics in live cells and animals - Nature Communications
DNA damage threatens genome stability, but its dynamics in living systems remain difficult to track. Here, the authors engineer MCPH1-based protein probes that specifically recognize γH2AX, enabling r...
nature.com
Join us in Lunteren, the Netherlands on March 5 & 6, 2026 for the 32nd Dutch Cancer Biology meeting. We have two fantastic keynote speakers: @andrea-musacchio.bsky.social and @colindascheele.bsky.social and the rest of the program will be by early-career scientists. Info: www.dutchcancerbiology.nl
Revised version of our original Red1-Hop1-Mek1 story, together with @jweir.bsky.social lab now online @biorxivpreprint.bsky.social Check it out: www.biorxiv.org/content/10.1...
Organizational principles governing assembly and activation of the meiosis-specific Red1-Hop1-Mek1 complex
In mitosis, sister chromatids are preferred repair templates for homologous recombination, whereas in meiosis interhomolog-based repair is promoted. How this switch, which is a defining event in sexua...
biorxiv.org
Pancreatic cancer cells express cryptic peptides shared across patients that may be therapeutic targets, according to new research in Science.
The hunt for common tumor antigens
Pancreatic cancer cells express cryptic peptides shared across patients that may be therapeutic targets
scim.ag
Single kinetochores execute an ordered series of molecular events as the Spindle Assembly Checkpoint is silenced https://www.biorxiv.org/content/10.1101/2025.05.23.655733v1
A Conserved Disruption of the Nuclear Permeability Barrier in Meiosis is Controlled by a Kinase-Phosphatase Pair in Saccharomyces cerevisiae https://www.biorxiv.org/content/10.1101/2025.05.14.654091v1
astounding yet also a reminder of how diverse life is -- often there are many different solutions to the same problem, but we're only aware of the ones on-hand (usually our own)
Wow: check it out; these fungi distribute their chromosomes across different nuclei! Normally each nucleus has a complete set of all chromosomes. Distribution of haploid chromosomes into separate nuclei in two pathogenic fungi | Science www.science.org/doi/10.1126/...
Excited to share our latest from my postdoc at @mskcancercenter.bsky.social in the Sfeir Lab, in collaboration with the Simon Powell Lab! We uncovered a novel genome repair mechanism in human cells: RNA-templated DNA double-strand break repair (RT-DSBR). (1/5)
Super excited to share my latest review! In this piece, I dive into how cells cleverly reuse proteins for mitosis-specific tasks — a fascinating and still underexplored area. There’s so much more to uncover, and I hope this review sparks new ideas and discussions! pubs.acs.org/doi/10.1021/...
Multitasking Proteins: Exploring Noncanonical Functions of Proteins during Mitosis
This review provides a comprehensive overview of how mitotic cells drive the repurposing of proteins to fulfill mitosis-specific functions. To ensure the successful completion of cell division, the cell strategically reallocates its “workforce” by assigning additional functions to available proteins. Protein repurposing occurs at multiple levels of cellular organization and involves diverse mechanisms. At the protein level, proteins may gain mitosis-specific functions through post-translational modifications. At the structural level, proteins that typically maintain cellular architecture in interphase are co-opted to participate in mitotic spindle formation, chromosome condensation, and kinetochore assembly. Furthermore, the dynamic reorganization of the nuclear envelope and other organelles relies on the temporary reassignment of enzymes, structural proteins, and motor proteins to facilitate these changes. These adaptive mechanisms underscore the remarkable versatility of the cellular proteome in responding to the stringent requirements of mitosis. By leveraging the existing proteome for dual or multiple specialized roles, cells optimize resource usage while maintaining the precision needed to preserve genomic integrity and ensure the survival of the next generation of cells.
pubs.acs.org
It’s out! The evolutionary origins of yeast point centromeres uncovered! “Ancient co-option of LTR retrotransposons as yeast centromeres” www.biorxiv.org/content/10.1...
Ancient co-option of LTR retrotransposons as yeast centromeres
The evolutionary origins of the genetic point centromere in the brewer's yeast Saccharomyces cerevisiae, a member of the order Saccharomycetales, are still unknown. Competing hypotheses suggest that t...
biorxiv.org
Looking for a student or postdoc! Want to combine evolutionary analysis + structural modeling with in vitro biochemistry & fluorescence microscopy? Help us uncover new protein-protein interactions — from in silico to in vitro. Join us at @istaresearch.bsky.social 👉 looselab.org 🧬💡🔬🎡
looselab.org
A must for all DNA repair aficionados! Egmond DNA Repair Meeting → April 19–24, 2026 🇳🇱 ✔️ Confirmed top speakers ✔️ Ample opportunities for talks & posters Don’t miss it: dnarepairmeeting-egmond2026.com
In vitro reconstitution by Peter Bieling, William Bement and collaborators reveals mechanistic principles of Rho GTPase activity patterning at cellular membranes, and stage-specific roles of regulators www.embopress.org/doi/full/10....
New preprint drop! Check out work from @jimmy-ly.bsky.social et al for how protein isoforms generated by alternate translation initiation create dual localization, contribute to mitochondrial function, and are mutated in disease. "Blue-tutorial" thread below. www.biorxiv.org/content/10.1...
Alternative start codon selection shapes mitochondrial function during evolution, homeostasis, and disease
Mitochondrial endosymbiosis was a pivotal event in eukaryotic evolution, requiring core proteins to adapt to function both within the mitochondria and in the host cell. Here, we systematically profile...
biorxiv.org
Countdown to an epic new pre-print. Mitochondria are cells within our cells. They need the same core activities - replication, transcription, translation. How do cells enable these diverse activities in both compartments? We uncover an unexpected + broad strategy with ancient origins. Stay tuned!
Wonderful, thought-provoking review by Sir Adrian Bird on cohesin loop extrusion as disrupter of chromatin organisation rather than generator. Great read! www.sciencedirect.com/science/arti...
Cohesin as an essential disruptor of chromosome organization
Cohesin is a multi-subunit molecular machine that is able to create lateral chromatin loops within a linear chromosome fiber. Despite intense study, a…
sciencedirect.com