Realistic life size replica model of Woolly Mammoth with skeleton fossil at Shanghai Natural History Museum. (Credit: AKKHARAT JARUSILAWONG on Shutterstock)
Frozen in time, the world’s oldest RNA ever recovered helps reveal the health, diet, and behaviors of extinct animals at time of death.
In A Nutshell
- Researchers successfully extracted RNA from a woolly mammoth that died about 39,000 years ago, more than doubling the previous age record for preserved genetic material of this type.
- The RNA revealed which genes were actively working in the mammoth’s muscle tissue at the time of death, showing an abundance of slow-twitch muscle fibers used for endurance.
- Genetic tests surprisingly revealed the mammoth was male, contradicting the original classification based on external anatomy.
- While DNA acts like a blueprint, RNA provides a snapshot of cellular activity, potentially allowing scientists to determine what extinct animals were eating, their health status, or even seasonal behaviors.
Akin to a text message sent tens of thousands of years ago, scientists have successfully decoded genetic instructions that were actively running inside muscle cells inside a frozen woolly mammoth the moment the animal died close to 40,000 years ago.
A team at Stockholm University successfully recovered RNA molecules from a juvenile mammoth named Yuka, revealing which genes were switched on in its skeletal muscle about 39,000 years ago. The findings, published in Cell, document the oldest ancient RNA recovered to date, more than doubling the previous record.
“We gained access to exceptionally well-preserved mammoth tissues unearthed from the Siberian permafrost, which we hoped would still contain RNA molecules frozen in time,” says lead author Emilio Mármol, formerly a postdoctoral researcher at Stockholm University, now based at the Globe Institute in Copenhagen. “We found signs of cell stress, which is perhaps not surprising since previous research suggested that Yuka was attacked by cave lions shortly before his death.”
DNA may get all the attention because it sticks around in fossils, but DNA is just the instruction manual. RNA is what actually builds proteins, regulates genes, and generally runs the machinery that keeps cells alive. Recovering ancient RNA means scientists can now see what mammoth cells were doing at or near the time of death, not just what they could have done.
Reading a Cellular Snapshot
When researchers analyzed Yuka’s muscle tissue, they found over 300 different messenger RNA molecules. These weren’t random fragments. They were genes with very specific jobs in muscle function.
The most abundant included titin and obscurin, which maintain muscle structure, and nebulin, which controls how muscle fibers assemble. The team even figured out what type of muscle Yuka had been using. Based on which genes were active, the tissue came from slow-twitch muscle fibers. These are the kind used for endurance rather than quick sprints.
“The presence of MYH7, TNNT1, and TNNC1, as well as TPM2 transcripts among the most abundant and reliably detected protein-coding mRNAs is indicative of an enriched presence of slow-twitch skeletal muscle fibers,” the authors wrote.
How Does RNA Even Survive?
Every biology student learns that RNA breaks down fast. It’s a single-stranded molecule that gets destroyed by enzymes within hours, sometimes minutes, of a cell dying. Textbooks say you need special chemicals to preserve it even in modern lab samples.
Permafrost rewrites those rules. When temperatures stay consistently below freezing, enzymes stop working. Bacteria can’t decompose tissue. Fungi can’t grow. Molecules that should disintegrate in hours can last millennia instead.
The research team tested 10 different mammoths. Only three had usable RNA, and Yuka blew the others away in quality. Scientists verified the RNA was genuine by looking for damage patterns that only show up in truly ancient molecules and by comparing it to DNA from the same tissues.
A Mammoth Gender Mystery
While analyzing Yuka’s RNA, researchers spotted something odd: genes from the Y chromosome. Specifically, a gene called USP9Y that only males have.
That was a problem. When Yuka’s frozen body was discovered in 2010, scientists examined the remains and classified the mammoth as female based on what looked like female anatomy.
So the team went back and tested DNA from Yuka multiple times, using different tissue samples. Every single test came back male. They even found mammoth-specific mutations in the SRY gene, which triggers male development.
Either Yuka had a developmental condition that gave a genetically male mammoth female-appearing anatomy, or the original examination simply got it wrong. The mystery remains unsolved.
Why RNA Changes Everything
DNA sequencing has revolutionized our understanding of extinct animals. Scientists have mapped woolly mammoth genomes, tracked how populations changed over thousands of years, and discovered new species.
But DNA only tells you what was possible. Every cell in a mammoth’s body had the same DNA whether it was muscle, liver, brain, or skin. What makes cells different isn’t their genetic code but which genes they turn on or off.
That’s what RNA reveals. A muscle cell makes different RNA than a liver cell. A stressed cell makes different RNA than a healthy one. RNA shows what was actually happening at a specific moment in time.
When researchers compared Yuka’s muscle RNA to modern human tissues, it matched human skeletal muscle, not brain or liver or anything else. The RNA also showed abundant ribosomal and transfer RNA molecules involved in making proteins, plus lots of mitochondrial genes. It’s exactly what you’d expect in muscle tissue with high energy demands.
The technique also identified two candidate microRNA genes. One appears in elephants, mammoths, and some other mammals but not in marsupials or sloths. The other may be specific to elephantids (elephants and mammoths). Both need laboratory validation.
What Comes Next
Yuka pushes the timeline back dramatically, but raises new questions. Could researchers determine what an extinct animal ate by looking at digestive enzyme RNA? Whether it was sick based on immune genes? Whether it was pregnant based on hormones? Maybe even figure out migration patterns from seasonal gene expression changes?
There is, however, a catch. This only works under very specific conditions. Seven of the 10 mammoths tested produced no usable RNA at all. Moreover, the fragments that do survive are tiny. Yuka’s longest was only 97 nucleotides compared to hundreds or thousands in fresh tissue. That makes analysis tough.
“Our results demonstrate that RNA molecules can survive much longer than previously thought. This means that we will not only be able to study which genes are ‘turned on’ in different extinct animals, but it will also be possible to sequence RNA viruses, such as influenza and coronaviruses, preserved in Ice Age remains,” explains study co-author Love Dalén, a professor of Evolutionary Genomics at Stockholm University and the Centre for Palaeogenetics.
So far, this approach only works with soft tissue preserved in permafrost. Most fossils are bones and teeth, not frozen muscle. Expanding beyond mummified specimens remains a major challenge.
For the specimens that do have preserved RNA, scientists now have access to information they never thought possible. Put succinctly, a molecular snapshot of cellular life from tens of thousands of years ago, revealing not just what extinct animals were, but what they were doing when they died.
Paper Summary
Limitations
The study only examined permafrost-preserved soft tissues from woolly mammoths. Most fossils consist of bones or teeth rather than mummified soft tissue, and whether the technique works on skeletal remains is unknown.
RNA isolation methods weren’t fully optimized and may benefit from improvements. The 23 PCR cycles used during sequencing may have favored certain RNA types over others. Some DNA contamination occurred in RNA samples, though amounts were minimal and likely unavoidable given low RNA yields.
Funding and Disclosures
Research was funded by Villum Fonden, Swedish Research Council, European Union (ERC grant PrimiGenomes), Tromsø forskningsstiftelse, Knut and Alice Wallenberg Foundation, Austrian Science Funds, European Molecular Biology Organization, and SciLifeLab programs.
One author (L.D.) serves on the scientific advisory board at Colossal Biosciences. No other conflicts were declared.
Publication Information
Authors: Emilio Mármol-Sánchez, Bastian Fromm, Nikolay Oskolkov, Kevin J. Peterson, Marc R. Friedländer, Love Dalén, and 12 co-authors from Stockholm University, Centre for Palaeogenetics, University of Tromsø, Lund University, Dartmouth College, and other institutions.
Journal: Cell, published online November 14, 2025 (open access)
Data: NCBI BioProject PRJNA1190340 and PRJNA1256124; code at github.com/emarmolsanchez/aRNA







