Tuesday, February 03, 2026

 

Scientists unravel vines’ parasitic nature



New study unlocks formula that explains vines’ ability to search for and attach to host plants



New York University

A climbing vine 

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A climbing vine in Oaxaca, Mexico.

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Credit: Lena Hunt/New York University





Twisting upwardly on trees and other plants—along with houses and even lampposts—vines are a wonder of nature. However, their marvels mask their parasitic behavior: in attaching to other life forms, vines block sunlight necessary for growth and strangle their hosts, preventing the flow of water and other nutrients.

While these threats were widely known, less clear is what gives vines their searching, attaching, and climbing capabilities. 

An international team of scientists has now unlocked a formula that enables vines to search for and attach to host plants—rapid elongation, directional movement, and the production of specialized contacting cells—and identified the gene family that engineers this formula. 

“Our research shows how molecular mechanisms are linked to plant movement—something we haven’t clearly understood,” explains Joyce Onyenedum, an assistant professor of environmental studies at New York University and an author of the study, which appears in the journal the New Phytologist. “Crucially, it gives us greater insight into these ropey parasites. They pose an ongoing menace to trees and other plants—among nature’s best tools for storing atmospheric carbon dioxide.”

It has been well-established that large tree branches bend through the production of fiber cells, called “G-fibers”, which are specialized cells that contract. In a study published last year, Onyenedum and her colleagues reported that G-fibers were common within the stems of vines. But the actual role of these cells was unclear.

In the New Phytologist study, Onyenedum and her colleagues, who included Lena Hunt, an NYU postdoctoral researcher, and Charles Anderson, a Penn State biologist, sought to address this question. 

To do so, the scientists studied common bean vines, which are cultivated globally, often seen in home gardens, and grow vertically. Specifically, they studied the role of a particular hormone, brassinosteroid, which is known to regulate plants’ developmental processes, including elongation, by comparing growth in a normal bean vine to one that was engineered to produce an excess amount of this hormone. 

These excess hormones repressed the development of G-fiber cells and produced “lazy vines” that elongate too fast and move in directionless manner.

This timelapse video shows the two bean vines—the left plant has hormone levels typically found in vines and climbs normally; the right plant, by contrast, has an excess amount of hormones, creating an imbalance that stifles climbing (video courtesy of the Onyenedum Lab/New York University).

The researchers also identified a candidate gene, XTH5, which is fundamental in plants’ structural growth and is specifically expressed during G-fiber development—thus potentially spotting the key actor supporting the coiling and gripping of vines.

“Genes like XTH5 allow plants to remodel their cell walls, which are complex structures that provide strength and flexibility to plants. This study demonstrates that cell wall remodeling is a critical component of plant movements such as twining,” says Anderson. 

“Our work shows that rapid elongation, directional movement, and the production of certain cells facilitates the maneuvering and eventual attachment of vines upon their host, thus unlocking the secrets to their behavior,” concludes Onyenedum. 

The study also included researchers from the New York Botanical Garden, Brazil’s Federal University of Rio Grande do Sul, and the University of Michigan.

This research was supported by an CAREER Award from the National Science Foundation (240167).

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Timelapse video shows the two bean vines [VIDEO] 

This timelapse video shows two bean vines—the left plant has hormone levels typically found in vines and climbs normally; the right plant, by contrast, has an excess amount of hormones, creating an imbalance that stifles climbing.

Credit

The Onyenedum Lab/New York University

 

Surgical innovation cuts ovarian cancer risk by nearly 80%



New UBC research shows that a simple surgical add-on can dramatically reduce rates of the most lethal gynaecological cancer




University of British Columbia





A prevention strategy developed by Canadian researchers can reduce the risk of the most common and deadly form of ovarian cancer by nearly 80 per cent, according to a new study published today in JAMA Network Open by researchers at the University of British Columbia (UBC). 

The strategy, known as opportunistic salpingectomy (OS), involves proactively removing a person’s fallopian tubes when they are already undergoing a routine gynaecological surgery such as hysterectomy or tubal ligation, commonly called “having one’s tubes tied”.  

The Canadian province of British Columbia (B.C.) became the first jurisdiction in the world to offer OS in 2010, after a team of researchers from UBC, BC Cancer and Vancouver Coastal Health designed the approach when it was discovered that most ovarian cancers originate in the fallopian tubes rather than the ovaries. OS leaves a person’s ovaries intact, preserving important hormone production so there are minimal side effects from the added procedure.  

The new study, led by a B.C.-based international collaboration called the Ovarian Cancer Observatory, provides the clearest evidence yet that the Canadian innovation saves lives. 

“This study clearly demonstrates that removing the fallopian tubes as an add-on during routine surgery can help prevent the most lethal type of ovarian cancer,” said co-senior author Dr. Gillian Hanley, an associate professor of obstetrics and gynaecology at UBC. “It shows how this relatively simple change in surgical practice can have a profound and life-saving impact.”  

New hope against a deadly cancer 

Ovarian cancer is the most lethal gynaecological cancer. Approximately 3,100 Canadians are diagnosed with the disease each year and about 2,000 will die from it.   

There is currently no reliable screening test for ovarian cancer, meaning that most cases are diagnosed at advanced stages when treatment options are limited and survival rates are low. 

The OS approach was initially developed and named by Dr. Dianne Miller, an associate professor emerita at UBC and gynaecologic oncologist with Vancouver Coastal Health and BC Cancer. She co-founded B.C.’s multidisciplinary ovarian cancer research team, OVCARE.  

"If there is one thing better than curing cancer it's never getting the cancer in the first place," said Dr. Miller.   

The new study is the first to quantify how much OS reduces the risk of serous ovarian cancer—the most common and deadly subtype of the disease. It builds on previous research demonstrating that OS is safe, does not reduce the age of menopause onset, and is cost-effective for health systems. 

The study analyzed population-based health data for more than 85,000 people who underwent gynaecological surgeries in B.C. between 2008 and 2020. The researchers compared rates of serous ovarian cancer between those who had OS and those who had similar surgeries but did not undergo the procedure.  

Overall, people who had OS were 78 per cent less likely to develop serous ovarian cancer. In the rare cases where ovarian cancer occurred after OS, those cancers were found to be less biologically aggressive. The findings were validated by data collected from pathology laboratories from around the world, which suggested a similar effect. 

From B.C. innovation to global impact 

Since its introduction in B.C. in 2010, OS has been widely adopted, with approximately 80 per cent of hysterectomies and tubal ligation procedures in the province now including fallopian tube removal. 

Globally, professional medical organizations in 24 countries now recommended OS as an ovarian cancer prevention strategy, including the Society of Obstetrics and Gynaecology of Canada, which issued guidance in 2015.   

“This is the culmination of more than a decade of work that started here in B.C.,” said co- senior author Dr. David Huntsman, professor of pathology and laboratory medicine and obstetrics and gynaecology at UBC and a distinguished scientist at BC Cancer. “The impact of OS that we report is even greater than we expected.”  

The researchers say expanding global adoption of OS could prevent thousands of ovarian cancer cases worldwide each year.  

Extending OS to other abdominal and pelvic surgeries where appropriate could further increase the number of people who could benefit from the prevention strategy. B.C. recently became the first province to expand OS to routine surgeries performed by general and urologic surgeons through a project supported by the Government of B.C. and Doctors of BC.  

“Our hope is that more clinicians will adopt this proven approach, which has the potential to save countless lives,” said Dr. Huntsman. “Not offering this surgical add-on may leave patients unnecessarily vulnerable to this cancer.” 

Interview language(s): English 

 

New discovery sheds light on evolutionary crossroads of vertebrates   




University of St. Andrews
Juvenile Ciona Seasquirt 

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Juvenile Ciona Seasquirt

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Credit: Shunsuke Sogabe





New research from the University of St Andrews has discovered a crucial piece in the puzzle of how all animals with a spine - including all mammals, fish, reptiles and amphibians - evolved.   

In a paper published today (2nd February) in BMC Biology, researchers found an intriguing pattern of gene evolution which appears to be significant for the evolutionary origin and diversification of vertebrates.   

All animals have major signalling pathways that their cells use to communicate with each other, which control things like how their embryos and organs develop. The signalling pathways are fundamental to animal development and are major targets in disease-causing mutations and for the development of pharmaceuticals.   

Proteins at the base of these signalling pathways are crucial as they control the final output from them, like a traffic system, directing cells into specific responses and gene expression.   

Researchers created new gene sequencing data in sea squirts, a lamprey and a type of frog. They found the genes that make these signalling output proteins have evolved in a distinctive way. The sea squirt is an invertebrate that helped to distinguish the change when moving from invertebrates to vertebrates. Lampreys are an early branch in the vertebrate group, which pinpoints that this change happened at the invertebrate-to-vertebrate transition.  

Researchers used long-molecule DNA sequencing, which allowed them to distinguish the different transcripts from each gene. Long-molecule sequencing had never been done on the genes expressed in these particular animals before. Therefore, researchers were able to characterise the real range of the transcripts and proteins produced from these genes in vertebrate development for the first time ever.  

Unlike the invertebrate sea squirt, the lamprey and frog made higher numbers of different forms of proteins from the individual signalling output genes, compared to all sorts of other types of genes.    

This significant change with the evolution of vertebrates is very striking. Given the importance of these pathways in how animals decide what types of cells, tissues and organs to make, it is highly likely these proteins have had a major role in making vertebrates (animals with backbones) different and more complex than invertebrates.   

Lead author of the study Professor David Ferrier from the School of Biology, said: “It was very surprising to us to see how this small selection of very particular genes stands out in the way that they are behaving compared to any other sort of gene we looked at.It will be exciting to determine how these various different protein forms work in distinct ways to generate the diversity of cell types we now see in vertebrates.”  

These diverse protein variations not only shed light on the origins of how we, and most other animals with backbones have evolved, but will also be important for future work on understanding how these proteins and pathways might be manipulated in disease management.  

 ENDS 

  

Adult Lamprey

Credit

Sebastian Shimeld



Xenopus Tadpole

Credit

Marika Salonna