Parts of Our DNA May Evolve Much Faster Than Previously Thought
The most comprehensive atlas of genetic change through generations shows the areas of the genome that evolve the fastest.
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Knowing how human DNA changes over generations is essential to estimating genetic disease risks and understanding how we evolved. But some of the most changeable regions of our DNA have been off-limits to researchers—until now.
A team of researchers from University of Utah Health, University of Washington, PacBio, and other institutions has used multiple DNA sequencing technologies to develop the most comprehensive atlas yet of genetic change through generations.
The new investigation revealed that parts of the human genome change much faster than was previously known, laying the foundations for new insights into the roots of human disease and evolution.
“It’s mutations that ultimately differentiate us from other species,” says author Lynn Jorde, PhD. “We’re getting at a very basic property of what makes us human.”
The biological “speed of light”
By comparing the genomes of parents to their children, the researchers could detect how often new mutations occurred and were passed down, a rate that Jorde says is as fundamental to understanding human biology as the speed of light is for understanding physics. “This is something you really need to know—the speed at which variation comes into our species,” says Jorde, professor of human genetics in the Spencer Fox Eccles School of Medicine (SFESOM) at the University of Utah. “All of the genetic variation that we see from individual to individual is a result of these mutations.” Over time, these changes have led to everything from differences in our eye color to the ability to digest lactose to rare genetic diseases.
The researchers estimate that every human has nearly 200 new genetic changes that are different from either parent. Many of these changes occur in regions of DNA that are especially difficult to study.
Aaron Quinlan, PhD, professor and chair of human genetics in SFESOM and an author on the study, says that previous efforts to study human genetic change were limited to the parts of the genome that mutate the least. But the new study used advanced sequencing technologies to reveal the most rapidly changing regions of human DNA—regions that Quinlan describes as “previously untouchable.”
“We saw parts of our genome that are crazy mutable, almost a mutation every generation,” he says. Other segments of DNA were more stable.
Jorde says that the new resource can be an important support for genetic counseling by helping answer the question, “If you have a child who’s affected with a disease, is it likely to be inherited from a parent, or is it likely to be a new mutation?” Diseases caused by changes in “mutation hotspots” are more likely to be unique to the child, rather than having been passed down from their parents. This means that the risk of the parents having other kids with the same disease is lower. But if a genetic change was inherited from the parents, those parents’ future kids have a higher risk of having the disease.
The platinum pedigree
The researchers’ discovery hinged on a Utah family that has worked with genetics researchers since the 1980s as part of the Centre d’Etude du Polymorphisme Humain consortium, proving invaluable for the Human Genome Project.
Four generations of the family have donated DNA and consented to its analysis, which allowed the researchers an extraordinarily in-depth look at how new changes arise and are inherited from parents to children. “A large family with this breadth and depth is an incredibly unique and valuable resource,” says Deborah Neklason, PhD, research associate professor of internal medicine in SFESOM and an author on the study. “It helps us understand variation and changes to the genome over generations in incredible detail.”
Reference: Porubsky D, Dashnow H, Sasani TA, et al. Human de novo mutation rates from a four-generation pedigree reference. Nature. 2025. doi: 10.1038/s41586-025-08922-2
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