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2025 Beddington Medal Winner: Rory Maizels

The Beddington Medal is the BSDB’s major commendation to promising young biologists, awarded for the best PhD thesis in Developmental Biology defended in the year previous to the award. Rosa Beddington was one of the greatest talents and inspirational leaders in the field of developmental biology. Rosa made an enormous contribution to the field in general and to the BSDB in particular, so it seemed entirely appropriate that the Society should establish a lasting memorial to her. The design of the medal, mice on a stylised DNA helix, is from artwork by Rosa herself.

Like many years, it was a tough decision for the BSBD committee to choose a winner for the 2025 Beddington medal. We are pleased to announce that this goes to Rory Maizels, for his PhD work at the Crick Institute on differential signal interpretation and cell fate decisions in the developing neural tube.

I am writing to enthusiastically support Rory Maizels’s nomination for the Beddington Medal. His PhD work represents a remarkable achievement that advances our field’s long-standing goal: developing dynamical models that capture the full complexity of developmental systems. The central challenge in developmental biology is to understand how complex, multicellular tissues emerge from the coordinated actions of individual cells. While we have made great strides in identifying key molecular players and mapping gene regulatory networks, we still lack the ability to create predictive dynamical models that capture development in its full complexity. Rory’s work represents a critical step toward addressing this fundamental challenge. What sets Rory’s contribution apart is both its comprehensive scope and meticulous execution. Rather than pursuing flashy but superficial advances, he focused on building robust foundations – developing and rigorously validating new experimental and computational approaches that together enable dynamic modelling of development at scale. Remarkably, Rory personally drove every aspect of the project: from optimising molecular biology protocols and establishing automated laboratory workflows, to designing novel machine learning frameworks for analysing the resulting data. This rare combination of experimental and computational expertise allowed him to iterate between theory and practice in a uniquely effective way.

Prior to his PhD, Rory built a strong foundation through diverse research experience: molecular biology at LMCB UCL, developing computational tools for mitochondrial research at Oxford (resulting in an eLife publication), and completing the prestigious Frank Knox Fellowship at Harvard in Computational Science and Engineering. It is important to emphasise that this fellowship was not simply a bioinformatics MSc but a computational course aimed at engineers and data scientists. This unique background prepared him perfectly for tackling the emerging challenges in single-cell genomics and developmental biology. At the Crick, he quickly demonstrated exceptional independence and scientific maturity, showing deep knowledge of the field while working autonomously and effectively communicating complex ideas to others.

In the first months in the lab (during the COVID pandemic), Rory led the computational analysis of a major single-cell RNA sequencing study of human neural development, analysing data from multiple stages of embryonic spinal cord tissue to identify distinct cell types and map differentiation pathways. His analysis not only revealed the diversity of neural cell types and their developmental trajectories but also provided important comparative insights between human and mouse development, demonstrating both his technical capabilities and his ability to collaborate effectively on complex projects. This work is published.

In his main PhD project, Rory developed novel experimental and computational methods. This delivered three major technical innovations that together advance our ability to study developmental dynamics. First, he developed sci-FATE2, an optimized and semi-automated protocol for metabolic labelling and single-cell RNA sequencing that matches commercial platforms in quality while being simpler to implement. This is published as a methods paper. Second, he created Velvet, a deep learning framework that improves upon existing methods for inferring cell state transitions from RNA data by integrating neighbourhood information into its velocity calculations. Finally, he extended this work with VelvetSDE, a cutting-edge neural stochastic differential equation system that can predict long-term cell fate trajectories and identify key decision points in development, while capturing the inherent variability in cellular decision-making. Applying this to data from the neural tube led to the realisation that expression of Shh modulators are crucial for differential signal interpretation and cell fate decision in the developing neural tube. This combination of experimental and computational advances provides a robust framework for studying the complex dynamics of development at unprecedented scale and resolution. The work recasts single-cell analyses from descriptions of observed data to models of the dynamics that generated them, providing a framework for investigating developmental fate decisions. This work is published.

Rory’s unique combination of creativity, determination, and technical expertise is responsible for the success of the project. His exceptional strengths in both experimental and computational approaches, spanning molecular biology to machine learning, gives him an ability to tackle complex biological problems from multiple angles. But his ability is not limited to technical skills. He is a deep thinker and has developed a clear and far-reaching view of the future of developmental biology. These scholarly capabilities are evidenced by his invited review on single-cell transcriptomics, which he authored independently following a well-received presentation at the Royal Society. We are also completing an article that sets out a vision for developmental biology in the single cell genomics era. In short, Rory is both a thinker and a doer.

The impact of Rory’s work is already evident in the catalytic effect it is having in the field. It has attracted substantial funding (three grants: CRUK Development, Crick I2I Funding, BBSRC project grant) and underpins five new projects in the lab, including single-cell screening of glioma transcription factors, timeresolved sequencing of organoids, and targeted sequencing approaches. Beyond our group, it has enabled new collaborations in cancer screening, neurodegeneration research, and immunology with leading labs. Most notably, this work formed the foundation for Rory’s successful fellowship application for post-doc at EBI and Sanger, where he will further develop these approaches.

Rory exemplifies the qualities we hope to cultivate in our field: deep theoretical understanding combined with practical capability, rigorous methodology alongside creative vision, and the ability to both conceive and execute transformative research. He is not just technically accomplished but a profound thinker about the future of developmental biology and a clear communicator. His work demonstrates both the insight to identify fundamental challenges and the skill to address them systematically.

Given the extraordinary breadth and depth of his contributions, his proven ability to execute complex interdisciplinary projects, and the clear impact his work is already having on the field, I believe Rory Maizels is an outstanding recipient of the Beddington Medal. He represents the kind of scientist who will help lead our field into its next phase, where we can finally begin to build a comprehensive understanding of development.

James Briscoe

 

Papers:

Maizels, R. J., and Briscoe, J. (2025). Gene regulatory networks: from correlaCve models to causal explanaCons. In prepara(on.

Maizels, R. J. (2024). A dynamical perspecCve: moving towards mechanism in single-cell transcriptomics. Philos. Trans. R. Soc. B

Maizels, R. J., Snell, D. M., and Briscoe, J. (2024). ReconstrucCng developmental trajectories using latent dynamical systems and Cme-resolved transcriptomics. Cell Systems

Maizels, R. J., Snell, D. M., and Briscoe, J. (2024). A protocol for Cme-resolved transcriptomics through metabolic labeling and combinatorial indexing. STAR Protocols

Rayon, T., Maizels, R. J., Barrington, C., and Briscoe, J. (2021). Single-cell transcriptome profiling of the human developing spinal cord reveals a conserved genetic programme with human-specific features. Development

2025 WOLPERT MEDAL WINNER: PLEASANTINE MILL

Following the sad passing of one of the greats of Developmental Biology, Lewis Wolpert, the BSDB committee has launched a new annual medal in his honour. Lewis was well known for his ability to distil our subject’s most engaging and fundamental problems into concise and well-grounded core concepts of Biology. This led to vastly important contributions to research in our field, but also to the communication of its problems to a broader audience. Through teaching, popular science writing and acting as a spokesperson for Science as a whole, Lewis inspired many of us into the deeper study of Developmental Biology. Therefore, our annual ‘Wolpert medal’ is presented to an individual who has made extraordinary contributions to the teaching and communication of Developmental Biology.We are very happy to announce that this year’s  winner of the BSDB Wolpert medal is Prof. Pleasantine Mill from the University of Edinburgh.

 

We enthusiastically endorse Prof. Pleasantine Mill (Prof. of Cilia Biology at the University of Edinburgh and MRC Investigator at the MRC Human Genetics Unit, Edinburgh) for the Wolpert Medal. Prof. Mill is an outstanding Developmental Biologist who has enthused us and others in our own research topics in developmental biology. The reasons for nominating her are listed below:

• Leadership and community building

Prof. Mill has demonstrated exceptional initiative and leadership by keeping the global cilia community connected. Her efforts since the early 2020 lockdowns have kept lines of scientific communication open and fostered collaborations amongst a global community of researchers.

She has organised over 50 UK Cilia Network e-symposia which ran weekly during the peak of the pandemic lockdowns and now run quarterly. Given the importance of cilia in developmental processes, the e-symposia bring together a global and diverse network of developmental biologists and other scientists working on all aspects of cilia.

A major focus of the cilia e-symposia is to provide a platform and exposure to graduate students, ECRs and junior PIs. Her stewardship during the pandemic promoted scientific communication during challenging times for junior researchers and kept us all going.

• Promotion of understanding of developmental disorders

Prof. Mill has over 20 years of experience as a Developmental Geneticist. Throughout this time, she has advocated and campaigned for more funding for the study of rare developmental ciliopathies.

She is on the Scientific Advisory Board for Ciliopathy Alliance and Primary Ciliary Dyskinesia (PCD) Research (UK Patient Charities), member of the leadership team for the UK Cilia Network and the MRCs Congenital Anomalies Cluster. Through her many leadership roles, she has directed her efforts to promote research on rare developmental diseases. Her group has also undertaken important public engagement activities including the PCD Awareness Day in 2018 and PCD Family Day 2019.

• Championing voices for ECRs and junior PIs

Prof. Mill’s drive in her field of modeling rare developmental disorders and her passion for equitable science has inspired a diverse generation of new cell and developmental biologists, including us. As minority scientists with fledgling independent groups, we have both especially benefited from the platforms she created for research conducted by junior PIs. We are certain, like us, she has inspired countless other emerging developmental biologists.

For these and many other reasons, we feel strongly that Prof. Mill is fully deserving of a Wolpert Medal in recognition of her heroic efforts to promote equitable and open scientific communication and for inspiring a new wave of developmental biologists.

  • Girish Ram Mali
  • Raman Das

Join us to celebrate the 100-year anniversary of the Company of Biologists!

Biologists @ 100 – incorporating the BSDB spring meting

Registration Now Open

  • Dates: 24th-27th March 2025
    Primary location: ACC Liverpool, UK
    BSDB Organisers: Véronique Azuara, Anahi Binagui-Casas, Shankar Srinivas, Abigail Tucker
  • BSDB conference grants are available to attend this meeting. Apply here.

 

2025 will mark the 100-year anniversary of The Company of Biologists. As part of their celebrations, the Company will be organising Biologists @ 100, a unique conference that will bring together their different communities.

The conference will incorporate the Spring Meetings of the British Society for Developmental Biology (BSDB) and the British Society for Cell Biology (BSCB). It will further include a Society for Experimental Biology (SEB) one-day Satellite Meeting ‘Experimental biology and impact: solutions to climate change and biodiversity loss’, the Journal of Experimental Biology (JEB) Symposium ‘Sensory perception in a changing world’, and a one-day Disease Models & Mechanisms (DMM) programme ‘Interdisciplinary approaches to combatting antimicrobial resistance’.

In the plenary sessions, the keynote speakers will consider topics of importance to the whole biological community: climate change and biodiversity, health and disease and emerging technologies.

Registration and abstract submission are now open. To view the programme and register your interest, visit https://biologists.com/100-years/conference.

This conference provides the chance to network and socialise with a wide cross-section of the Cell and Developmental Biology community. We hope you can join us in March 2025 and we look forward to welcoming you!

BSDB Organising Committee

 

In memory of my mentor, colleague and friend, David Ish-Horowicz FRS

David Ish-Horowicz, who died on July 19th just two weeks short of his 76th birthday, pioneered the application of molecular biology to the analysis of Drosophila development in the UK. His laboratory at the Imperial Cancer Research Fund (ICRF) unit in Mill Hill performed ground-breaking studies that paved the way for the molecular revolution that has driven our subject over the last 40 years. He began by cloning and characterising the Drosophila gene hairy, identified as one of the pair-rule class by his friends and colleagues Christiane Nüsslein-Volhard and Eric Wieschaus, with whom he had worked in the laboratory of Walter Gehring in Basel. Later, in his lab at the legendary ICRF DBU (Developmental Biology Unit) in Oxford, he applied his skills to the identification and analysis of the Notch ligand, Delta, in vertebrates. His many accomplishments were recognized by the BSDB through the award of the Waddington Medal in 2007. He leaves an indelible mark on the field, both through his research and through the many PhD students and post-docs that he mentored.

 

I first met David exactly 44 years ago this month, at the 1980 EMBO Drosophila Workshop in Crete. This was a meeting reserved for principal investigators to which I had somehow gained admission, despite still being a mere PhD student. As I entered the reception on the first evening, I was feeling extremely nervous and intimidated by all the senior scientists gathered around chatting in groups and was desperately looking around the room for someone who might speak to me. And then I came across David, who, with his characteristic smile, engaged me in conversation about my research interests. He immediately put me at my ease and gave me the confidence to make the most of the meeting, something I will never forget.

Eighteen months later I saw an advertisement for a research fellowship in David’s lab and did not hesitate to apply. David invited me for interview at the ICRF labs in Mill Hill, an experience that for me was both exhilarating and life-changing. We talked all day about how fruit fly embryos develop and his plans to understand the function of the “hairy” gene that he had just succeeded in cloning – one of the first of the so-called segmentation genes to be isolated molecularly. The combination of David’s razor-sharp mind and child-like enthusiasm was irresistible and I did not think twice about accepting when he offered me the post. So began three of the most exciting years of my scientific career. David’s thirst for knowledge was infectious and I could not wait to get into the lab each day to see what new phenomena we would uncover.

The joy of making new discoveries – be they inside or outside the lab – is something David never lost. Indeed, only a few weeks ago when I last visited David and Ros, his wife, in their flat in London, he excitedly told me that he had discovered a new entrance to the Barbican Arts Centre! When he explained that this was located half-way down the ramp to the underground car park, I must admit that I did wonder if his illness (glioblastoma) might be playing tricks with his memory. But I happily agreed to go for a walk with him so that he could show me – and sure enough, as we descended the ramp into the carpark, there was the door that led us straight into the entrance foyer of the centre!

David’s satisfaction at having found the best route into the Barbican from his flat was palpable, a reflection of his constant quest to find the best way of doing everything. This trait was worth its weight in gold to those who worked in his lab – he consumed the scientific literature obsessively and could always tell you the latest and best ways of doing things, often prefaced by “what you should have done”! It was David who introduced me to SP6 polymerase, which revolutionized the synthesis of probes for in situ hybridization. The fact that this superseded the single stranded DNA probes, the synthesis of which David himself had perfected with his post doc, Julian Burke, was of no concern to him – he thrived on technological progress.

Outside the lab, David could always tell you the best places to ski, the best restaurants to eat at, the best wines to drink – the list was endless, informed by his voracious appetite for reading “Which”! There was only one occasion when he got things badly wrong: I had wanted to buy a HiFi so naturally sought his advice. He told me which turntable, amplifier and speakers to buy and which audio store to buy them from, in West Hampstead as it happened, which I duly visited one Saturday afternoon. The next Monday David asked excitedly if I had got everything – “yes” I replied “and I bought a CD player too!” David’s expression immediately changed and he shook his head: “no, no” he exclaimed, “CDs will be obsolete in a couple of years when Sony launch DAT (Digital Audio Tape)” That was in 1984!

Not only was David always happy to give advice, he was also incredibly generous with his time. I recall him staying late one evening to show me how to do colony lifts of a phage library that he had helped me construct in an effort to clone the trithorax gene, something he encouraged me to do in my “spare” time. We did this in his cramped and cluttered lab-cum-office whilst listening to the Archers on the radio! Many years later, after I had moved away from the DBU in Oxford – where we had been colleagues for nearly 10 years – and established what was to become an MRC Centre in Sheffield, I asked David if he would serve on its Scientific Advisory Board. He agreed without hesitation; and most recently it was David to whom I turned when I needed an external assessor on an appointments panel for the Living Systems Institute in Exeter, a role he fulfilled with his customary thoroughness, insight and good humor.

David began his scientific career sequencing a tRNA – he has left us enriched by the qualities denoted by the much shorter sequence of a well-known restriction site, CCGG: Caring, Compassionate, Generous, Genius.

Thank you for everything David – I will miss you.

Philip Ingham FRS

Raymond Schinazi and Family Chair of Life Sciences

University of Bath

2024 BSDB BEDDINGTON MEDAL WINNER: DELAN ALASAADI

The Beddington Medal is the BSDB’s major commendation to promising young biologists, awarded for the best PhD thesis in Developmental Biology defended in the year previous to the award. Rosa Beddington was one of the greatest talents and inspirational leaders in the field of developmental biology. Rosa made an enormous contribution to the field in general and to the BSDB in particular, so it seemed entirely appropriate that the Society should establish a lasting memorial to her. The design of the medal, mice on a stylised DNA helix, is from artwork by Rosa herself.

Like many years, it was a tough decision for the BSBD committee to choose a winner for the 2024 Beddington medal. We are pleased to announce that this goes to Delan Alasaadi, for his PhD work at UCL on the role of tissue mechanics in neural crest induction.

 

I have written many letters on behalf of numerous students to support their applications for various prizes, jobs, and positions, including several previous Beddington Medal applications. However, writing a letter supporting Delan Alasaadi for this award comes with great ease, as Delan has been an excellent Ph.D. student.

Delan developed great curiosity; he continuously engaged with his colleagues in discussions during our lab meetings and beyond. With unique ambition, he sought novel ideas to test in his project. With impeccable determination, breaking the physical barrier, he established collaborations and sought expertise across Europe and other continents, learning the most challenging techniques and valuable lessons.

Delan’s PhD thesis was about the role that tissue mechanics could play in neural crest induction. This was a risky project because of the lack of tools to measure and modify mechanics in vivo. Delan spent the first part of his Ph.D. designing biophysical tools to investigate the feasibility of the question at hand, showing great creativity in his experimental approaches. Embryonic induction is the process by which a group of cells sends signals to adjacent tissues, changing their differentiation fate. An important aspect of embryonic induction, which has been poorly studied, is how the receiving tissue regulates the response to the inductive signals—a process known as ‘competence.’ Additionally, while the molecules involved in embryonic induction have been identified, the role of mechanical cues in this process has remained largely unexplored. Delan found that during early development, the hydrostatic pressure of the blastocoel cavity increases. This increase is sensed by the ectoderm cells above the cavity, modulating Yap activity, which in turn regulates the response to Wnt signaling—a key player during neural crest induction. Thus, Delan found, for the first time, the mechanism that could explain the loss of neural crest competence during development: the increased hydrostatic pressure leads to the retention of Yap/b-catenin in the cytoplasm, impairing neural crest induction even in the presence of the inducer Wnt (loss of competence). Delan showed that this mechanism is conserved in embryos of different species (e.g., amphibians, mice, humans). This work has been recently accepted in Nature Cell Biology (2024), with Delan as the sole first author.

There are two important aspects of how Delan approaches research that make him a deserving winner of the Beddington Medal:

Fearless and ambitious: There was not a single technique or experiment that Delan did not learn if he considered it necessary to address his PhD project. Consequently, he set up in my lab many techniques that we did not have, such as micropipette aspiration, microcomputed tomography, Micro-pressure probe (servo-null) to measure hydrostatic pressure, and in vivo biophysical tools among others.

 Commitment: Not only did he work countless hours and overcome the limitations of developing his PhD during the COVID-19 pandemic, but he also showed a commitment to his work and experiments that is difficult to find. Just one example: he wanted to measure the hydrostatic pressure inside the embryo, but there are only a few labs worldwide that have the equipment and expertise to do it. He found a lab in the Netherlands that could teach him the technique, but we failed to get a source of Xenopus embryos from the Netherlands; instead, we got embryos from Belgium. So, every day, Delan had to travel to Belgium in the morning, get recently fertilized embryos that he kept in a low-temperature incubator on the train, and rush back to the lab in the Netherlands to conduct the experiments. He succeeded!

In addition to his main Ph.D. work accepted in Nature Cell Biology, he is the co-first author of another paper published in Developmental Biology about neural crest migration and the first author in a two-author review to be published in the journal Cellular and Molecular Life Sciences titled “Mechanically guided cell fate determination in early development,” written entirely by Delan.

In conclusion, Delan has been the only and mighty driving force behind his PhD work, identifying for the first time that mechanics (hydrostatic pressure) controls embryonic competence. His findings resolve a 100-year-old question: how embryonic competence is regulated, and which implications in stem cell research and cell therapy approaches? He is a motivated and dedicated young researcher, and all his efforts deserve to be recognized with an award such as the Beddington Medal. Therefore, I support this application in the strongest way possible.

  • Roberto Mayor

Published work:

Alasaadi DN, Mayor R. Mechanically guided cell fate determination in early development. Cell Mol Life Sci. 2024 May 30;81(1):242. doi: 10.1007/s00018-024-05272-6. PMID: 38811420; PMCID: PMC11136904.

Alasaadi DN, et.al. Competence for neural crest induction is controlled by hydrostatic pressure through Yap. Nat Cell Biol. 2024 Apr;26(4):530-541. doi: 10.1038/s41556-024-01378-y. Epub 2024 Mar 18. PMID: 38499770; PMCID: PMC11021196.

Barriga EH, Alasaadi DN, et. al. RanBP1 plays an essential role in directed migration of neural crest cells during development. Dev Biol. 2022 Dec;492:79-86. doi: 10.1016/j.ydbio.2022.09.010. Epub 2022 Oct 4. PMID: 36206829.