ºÚÁϳԹÏÍø

© 2025 ºÚÁϳԹÏÍø

FCC Public Inspection Files:
· · ·
· · ·
Public Files Contact · ATSC 3.0 FAQ
Play Live Radio
Next Up:
0:00
0:00
0:00 0:00
Available On Air Stations

The unique genetic change that turned horses into athletic powerhouses

Horses are exceptional athletes, able to push their large bodies farther and faster than many other animals.
Darrell Gulin/Getty Images
/
The Image Bank RF
Horses are exceptional athletes, able to push their large bodies farther and faster than many other animals.

Gianni Castiglione did not set out to study horses.

The Vanderbilt University biologist and his colleagues were interested in how different animal species balance the need to produce energy with the harmful byproducts of that production.

"To make energy, we've made a deal with the devil to, basically, have a slow burning fire in our cells," he said. That fire essentially burns oxygen to create energy. But that kicks up a lot of smoke, or oxidative stress, that can harm cells.

Horses, it turns out, have evolved an unusual way of regulating this tradeoff that allows them to without incurring more cellular damage, researchers report in the journal Science. Those genetic changes may, in part, explain how horses became such powerful athletes, able to and outlast virtually all other animals.

"Horses can make this fire burn even hotter and make the damage even less than it would be in a species like a human," said Castiglione.

The changes occurred in a key gene pathway called NRF2/KEAP1. The pathway senses the buildup of oxidative stress and then kickstarts antioxidant production, which can clean it up, said Castiglione. "This is essentially the energy production and fire department, all wrapped in one."

Castiglione and his colleagues were scanning the genomes of nearly 200 mammalian species looking for unusual variants in this pathway. Horses stuck out with a single, highly unusual mutation.

"It's a type of mutation called a nonsense mutation," he said. "That's because it breaks a gene, it inactivates it from doing what the cell needs it to do." It basically put a stop sign, called a stop codon, toward the beginning of the KEAP1 gene. Stop codons generally signal where a gene ends, so having one at the start would "break" the gene.

This mutation kills mice, probably because it allows too much "smoke" to build up in cells. So Castiglione was stumped. "We thought, wow, how are horses dealing with this?"

Through a variety of genomic and molecular techniques, the researchers found an answer.

"Horses have evolved a very intricate strategy for working around this stop codon," said Elia Duh, a study co-author and molecular biologist at Johns Hopkins University. Essentially, a suite of mutations allows them to ignore the stop sign, making the gene work, but in a slightly different way that ends up benefiting the horses.

The researchers found that these mutations, which arose in the ancestors of all modern horses, allow their muscle cells to produce up to five times more energy than mouse cells, while simultaneously ramping up their damage-control system by 200%.

"This provides them with the biochemical means to run fast and over long distances," said Duh. This ultimately helps them become aerobic powerhouses.

"I really love this paper," said Samantha Brooks, a horse genetics researcher at the University of Florida. The mutation, she said, "should have caused a catastrophic loss of function for this protein. But instead, the ancestors of these species somehow managed to really turn that lemon into lemonade."

The way they made lemonade — ignoring a stop codon — has only previously been reported in viruses, the researchers say.

This adaptation could have implications for human health. Many inherited diseases, like and, stem from stop codons arising in important genes. If researchers can better understand how horses manage to ignore such stop codons, said Duh, perhaps they could develop gene therapies that do just that in humans, too.

Copyright 2025 NPR

The independent journalism and non-commercial programming you rely on every day is in danger.

If you’re reading this, you believe in trusted journalism and in learning without paywalls. You value access to educational content kids love and enriching cultural programming.

Now all of that is at risk.

Federal funding for public media is under threat and if it goes, the impact to our communities will be devastating.

Together, we can defend it. It’s time to protect what matters.

Your voice has protected public media before. Now, it’s needed again. Learn how you can protect the news and programming you depend on.

SOMOS CONNECTICUT is an initiative from ºÚÁϳԹÏÍø, the state’s local NPR and PBS station, to elevate Latino stories and expand programming that uplifts and informs our Latino communities. Visit CTPublic.org/latino for more stories and resources. For updates, sign up for the SOMOS CONNECTICUT newsletter at ctpublic.org/newsletters.

SOMOS CONNECTICUT es una iniciativa de ºÚÁϳԹÏÍø, la emisora local de NPR y PBS del estado, que busca elevar nuestras historias latinas y expandir programación que alza y informa nuestras comunidades latinas locales. Visita CTPublic.org/latino para más reportajes y recursos. Para noticias, suscríbase a nuestro boletín informativo en ctpublic.org/newsletters.

The independent journalism and non-commercial programming you rely on every day is in danger.

If you’re reading this, you believe in trusted journalism and in learning without paywalls. You value access to educational content kids love and enriching cultural programming.

Now all of that is at risk.

Federal funding for public media is under threat and if it goes, the impact to our communities will be devastating.

Together, we can defend it. It’s time to protect what matters.

Your voice has protected public media before. Now, it’s needed again. Learn how you can protect the news and programming you depend on.

Related Content