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21 August 2026
Decoding a stinging cell shaped by half a billion years of evolution
Postdoc Profile: Anna Klompen, Ph.D., on her Stowers research experience — "My experience at the Institute has been exceptional."
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Stowers Institute scientists found that the sea anemone Nematostella uses many of the same proteins humans rely on to make eggs and sperm, offering the potential for new insights into infertility, miscarriage, and birth defects
Key Highlights
KANSAS CITY, Mo. – October 23, 2026 – Every egg cell and sperm cell depends on meiosis, a tightly choreographed process in which chromosomes find their partners, exchange genetic material, and then divide. When meiosis goes awry in humans, the consequences can include infertility, miscarriage, and birth defects.
A new study from the Stowers Institute for Medical Research, published in Science Advances, shows that the molecular machinery guiding this process is more widely shared across animals than expected, and more flexible.
“That was one of the broader insights from the paper,” said Stowers Investigator and Graduate School President Matt Gibson, Ph.D. “Proteins and protein complexes may look very much the same, but nevertheless function in different ways.”
The project was led by Stefanie “Steffi” Williams, Ph.D., a Stowers Graduate School alum who is currently a postdoctoral fellow at the European Molecular Biology Laboratory. At the Institute, her work grew from a collaboration between Gibson's lab and the lab of the late R. Scott Hawley, Ph.D., a former Stowers Investigator and a pioneer in the field of meiosis.
In this latest study, Williams found that the sea anemone assembles a ladder-like structure called the synaptonemal complex between paired chromosomes, much as humans do. This structure contained eight of ten proteins known to make up the synaptonemal complex in humans.
“Despite their essential function, many of the proteins that coordinate meiosis show signatures of rapid evolution, changing much faster than normal housekeeping genes do,” said Williams. “So, I was fascinated to find older research showing that cnidarian genomes encode proteins clearly similar to those in humans, and I had to know whether they truly function in the same way.”

Male Nematostella
When Williams disabled three of these proteins, the results were unexpected. Mutations in two of them, sycp1 and syce2, caused female sterility. Males carrying the same mutations remained fertile, and loss of syce2 disrupted the stabilization of paired chromosomes only in females.
“When I first sat at the microscope and saw that some components are not required to synapse chromosomes, I thought I must have made a mistake because it didn’t make any sense,” said Williams. “Finding out that the architectural functions of synaptonemal complex proteins must have changed was totally unexpected.”
Until now, studies of these proteins in animals were largely limited to mice, fruit flies, and roundworms. Because Nematostella is transparent and its eight gonads can be observed directly in live animals, the findings suggest a new way to study meiosis in action, helping answer questions that might be difficult or impossible to address in mammals.
“This work establishes Nematostella as a good experimental system for understanding meiotic processes at a deeper level,” said Gibson. “The potential for live imaging could reveal new biology that’s difficult to observe in mammals, particularly at the cellular level.”

Spawning female Nematostella
As a member of the Stowers Graduate School, Williams first rotated in the Hawley Lab, studying meiosis in the fruit fly Drosophila. Williams then rotated into the Gibson Lab and began to work with Nematostella, a sea anemone and a relative of corals and jellyfish that is the focus of Gibson’s research.
“Scott inspired Steffi’s passion for meiosis,” said Gibson. “When she began working on sea anemones, she became interested in how it worked in these organisms where it hadn’t been explored before. This led to a collaboration between labs, and I felt lucky to benefit all along the way from Scott’s immense knowledge and Steffi’s excitement about the topic, which ultimately led to this new area of research.”
“Scott taught me to follow my passion regardless of what others may think of it, as well as the importance of teaching and good mentorship,” said Williams. “To this day, Scott inspires me to become a better scientist and human being.”
About the Stowers Institute for Medical Research
Founded in 1994 through the generosity of Jim Stowers, founder of American Century Investments, and his wife, Virginia, the Stowers Institute for Medical Research is a non-profit, biomedical research organization with a focus on foundational research. Its mission is to expand our understanding of the secrets of life and improve life’s quality through innovative approaches to the causes, treatment, and prevention of diseases.
The Institute consists of more than 20 independent research programs. Of the approximately 500 members, over 370 are scientific staff that include principal investigators, fellows, technology center directors, postdoctoral scientists, graduate students, and technical support staff. Learn more about the Institute at stowers.org and about its graduate program at stowers.org/gradschool.
Media Contact:
Joe Chiodo
Director of Communications
Stowers Institute for Medical Research
724-462-8529
joe.chiodo@stowers.org
News

21 August 2026
Postdoc Profile: Anna Klompen, Ph.D., on her Stowers research experience — "My experience at the Institute has been exceptional."
Read Article
Press Release
23 October 2026
Stowers Institute scientists found that the sea anemone Nematostella uses many of the same proteins humans rely on to make eggs and sperm, offering the potential for new insights into infertility, miscarriage, and birth defects
Read Article
Press Release

14 October 2026
Tissues constantly add cells as they grow but somehow remain organized. A new study from the Gibson Lab reveals how part of this complex, poorly understood process works — providing new insights into how tissues change during development, regeneration, and disease.
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