RNA Molecules Discovered in 39,000-Year-Old Woolly Mammoth Tissue

Researchers have successfully extracted and sequenced ancient RNA from the tissues of 10 woolly mammoths preserved in permafrost. One of these specimens is estimated to be 39,000 years old, making it the oldest ancient RNA sequence recorded to date.

Marmol Sanchez et al. Ancient RNA sequences identified in late Pleistocene woolly mammoth tissue. Image credit: Marmol Sanchez et al., doi: 10.1016/j.cell.2025.10.025.

Investigating prehistoric genes and their activation is crucial for understanding the biology and evolution of extinct species.

For years, scientists have been piecing together the mammoth genome and their evolutionary history through DNA analysis.

However, RNA, which indicates active genes, has remained elusive until now.

“With RNA, we can provide direct evidence of which genes are ‘turned on’ and gain insights into the final moments of mammoths that lived during the last Ice Age,” stated Dr. Emilio Marmol, a researcher at the Globe Institute.

“This kind of information cannot be obtained from DNA alone.”

In this study, Dr. Marmol and colleagues analyzed permafrost-preserved tissue from 10 late Pleistocene woolly mammoths discovered in northeastern Siberia, spanning from the central Indigirka region to the Oyogos Yar coast and the New Siberian Islands.

“We accessed exceptionally well-preserved mammoth tissue excavated from the Siberian permafrost, expecting it to contain RNA molecules that had remained frozen over millennia,” Marmol mentioned.

“We have pushed the limits of DNA recovery for over a million years,” said Professor Rav Dalen from Stockholm University and the Center for Paleogenetics.

“Now we aimed to determine if RNA sequencing could go further back than prior research.”

Researchers successfully identified tissue-specific gene expression patterns in the muscular remains of Yuka, a 39,000-year-old juvenile mammoth.

There are over 20,000 protein-coding genes in the mammoth genome, but not all are actively expressed.

The detected RNA molecules relate to proteins crucial for muscle contraction and metabolic regulation under stress.

Researchers also discovered several RNA molecules that regulate gene activity in mammoth muscle samples.

“We found non-protein-coding RNAs, such as microRNAs, which were among our most intriguing discoveries,” Dr. Mark Friedlander from Stockholm University’s Wenner-Gren Institute remarked.

“The muscle-specific microRNAs identified in mammoth tissue provide concrete evidence of gene regulation occurring in real-time in ancient eras. This is a groundbreaking achievement.”

The identified microRNAs also enabled the authors to confirm their findings originated from mammoths.

“We found a rare mutation in a specific microRNA, providing evidence that it is of mammoth origin,” noted Dr. Bastian Flom from the Norwegian Arctic University Museum.

“We also uncovered novel genes solely based on RNA evidence, a feat not attempted before at such ancient sites.”

“RNA molecules can endure for much longer than previously assumed.”

“Our findings demonstrate that RNA can survive much longer than previously thought,” Professor Dalen added.

“This allows us to not only explore which genes are ‘turned on’ in various extinct creatures but also to sequence RNA viruses like influenza and coronaviruses that are preserved in Ice Age remains.”

These findings were published in the Journal of Cell on November 14, 2025.

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Emilio Marmol-Sanchez et al. Ancient RNA expression profiles from extinct woolly mammoths. Cell published online on November 14, 2025. doi: 10.1016/j.cell.2025.10.025

Source: www.sci.news

Vascular Organoids Rapidly Repair Injured Tissue

Human vascular organoids created from stem cells

Melero Martin Lab at Boston Children’s Hospital

A new method using small, lab-grown vascular structures has effectively restored blood flow to injured tissue in mice, significantly reducing necrosis. This technique shows promise for mitigating damage caused by injuries or blood clots in the future.

Previously, researchers developed vascular organoids by immersing human stem cells in a mix of chemicals, a process that took weeks and often resulted in structures that did not accurately replicate natural blood vessels, according to Juan Melero-Martin from Harvard University.

In a new approach, Melero-Martin and his team genetically modified human stem cells derived from reprogrammed skin cells. By introducing a genetic sequence and the antibiotic doxycycline, they were able to create vascular organoids in just five days. “The resulting blood vessels exhibited protein and gene activity levels closely resembling those of natural human tissues,” notes Melero-Martin.

To evaluate the organoids’ ability to rehabilitate damaged tissue, the researchers surgically obstructed the blood supply to one leg of several mice, reducing blood flow to less than 10% of normal. After an hour, they introduced 1,000 organoids at the injury site.

Two weeks post-implantation, imaging revealed that the new blood vessels had integrated with the existing ones, restoring blood flow to approximately 50% of normal levels, as stated by Oscar Abiles at Stanford University. “In cases of heart attacks, restoring even this amount of blood flow can significantly minimize tissue damage.”

Post-treatment, about 75% of the mice exhibited minimal dead tissue, while in a control group without organoid treatment, nearly 90% experienced severe tissue death.

In additional trials, the team treated mice with type 1 diabetes with organoids, which had caused pancreatic damage and elevated blood glucose levels. They discovered that integrating organoids with pancreatic tissue transplantation greatly enhanced glycemic control compared to transplantation alone.

However, further studies involving larger animals such as pigs are essential before considering human trials, Abirez states. Melero-Martin anticipates that human research could begin within five years.

Besides facilitating tissue repair, these findings may lead to the development of lab-grown mini-organs that more accurately represent bodily functions or even mini-tumors for research and treatment testing.

“Until recently, organoids lacked blood vessels and could only grow to a limited size. Beyond a few millimeters, they began to perish,” explains Abirez. “This study offers a method to incorporate blood vessels into organoids, thus enhancing their fidelity to human physiology and aiding treatment development.”

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Source: www.newscientist.com

Paleontologists Uncover New Connective Tissue Structures in Dinosaurs

Paleontologists have uncovered evidence of previously unrecognized soft tissue structures in the cheek areas of various dinosaur species. This discovery deepens our understanding of dinosaur anatomy and underscores the limitations of current methods for reconstructing anatomical features that are not well preserved.



Soft tissue visualization of Edmontosaurus created through photography, 3D modeling, digital painting, and histology of bones in the Alberta Dinosaur Park, Canada. Image credit: Henry Sharp.

“Such examples of soft anatomy in dinosaurs are rare due to the degradation of muscles and tissue over time,” remarked Henry Sharp, a paleontologist from the University of Alberta.

“While bones can be excavated and assembled into semi-complete skeletons, for a long time, there was no effective way to discern the muscles and tissues present in dinosaurs.”

“In the 1990s, existing systematic brackets utilized the closest living relatives of dinosaurs—alligators and birds—to gain insight into their ’tissues and muscles.’

“However, this approach has its shortcomings: the muscles reconstructed in dinosaurs are those found in alligators and birds.”

“What if dinosaurs possessed their own unique muscles that aren’t present in their modern relatives, or if birds have lost or adapted their original musculature?”

“While examining a skull of Edmontosaurus, affectionately named Gary, I noticed a distinctive flange structure atop the bone near its prominent cheek.”

“As I delved deeper, I struggled to find answers.”

“There were large, corrugated sections of the skull. In a mammalian skull, I would interpret that as cheek muscle attachment. Yet, reptiles are not supposed to exhibit such muscle structures.”

“This sparked intrigue. What if this finding contradicted existing models of dinosaur musculature?”

To gain a clearer understanding of this aspect of dinosaur anatomy, Sharp and his colleagues from the University of Alberta, the University of Toronto, the Royal Museum of Ontario, and the University of New England began investigating similar regions in the skulls of other dinosaur species, uncovering evidence of analogous structures.

“The findings were consistently located in the same area. This strongly suggests that it represents a muscle or ligament,” Sharp explained.

To validate their hypothesis regarding this bone area being a site for some type of soft tissue structure, researchers meticulously cut thin sections of dinosaur bone.

“Soft tissues, such as muscles and ligaments, are anchored to the bone via collagen fibers,” Sharp stated.

“These fibers help secure the muscle or ligament, preventing detachment and potential injury to the animal.”

Once the soft tissue deteriorates, what remains are the collagen fibers, which can be examined through thin slices of bone under polarized light.

“It appears as if someone has fractured a bone at the surface and then scraped it with an X-acto knife,” Sharp noted.

The researchers employed a technique called sleepy to analyze various angles of the zygomatic and mandibular bone slices, enabling them to investigate the 3D orientation of the collagen fibers.

“These collagen fibers don’t insert haphazardly; they align with the angles where muscles attach,” Sharp added.

In all examined dinosaur species, collagen fibers manifested connections between the cheek and lower jaw, reinforcing the idea that the soft tissue structure resembles cheek muscles and ligaments.

Variation in the size and attachment angles across different dinosaur species suggests that this newly identified soft tissue played specialized roles, such as stabilizing the jaw and influencing feeding behavior.

“While we don’t fully understand its precise functions, it is evident that these soft tissues significantly impacted how these dinosaurs chewed.”

“This discovery underscores the importance of comparing dinosaur fossils with those of modern relatives for a more nuanced and accurate comprehension of extinct anatomy.”

“Dinosaurs exhibit considerable diversity, yet we often overlook significant aspects by attempting to interpret the past solely through the lens of contemporary conditions.”

Survey results were published in Journal of Anatomy.

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Henry S. Sharp et al. Skull morphology and histology reveal previously unexpected cheek soft tissue structures in dinosaurs. Journal of Anatomy, published on March 21, 2025. doi:10.1111/joa.14242

This article is a rendition of a press release provided by the University of Alberta.

Source: www.sci.news

Breakthrough in Personalized Medicine: Mini Organs Grown from Fetal Tissue by Scientists

A new breakthrough in medical research could lead to personalized therapy for babies in the womb. Scientists have successfully grown small organs, known as organoids, from fetuses for the first time. This allows for monitoring the health of the fetus by cloning its organs.

Organoids are complex 3D models of organs made from human cells, retaining the DNA of the original cells, in this case, amniotic fluid cells. These organoids mimic human tissue and provide a more detailed view of any malformations compared to traditional imaging techniques like MRI or ultrasound.

Developed by researchers at UCL and Great Ormond Street Hospital (GOSH), this new technology enables a functional assessment of a baby’s congenital condition before birth. This groundbreaking method does not involve access to fetal tissue and is a significant advancement in prenatal diagnosis.

Lead author Dr. Mattia Gerli highlights the potential of organoids to revolutionize the pharmaceutical industry and clinics, particularly in fetal development. The study focuses on utilizing amniotic fluid cells to create organoids for prenatal medicine.

Growth process of mini organs

The process involves extracting cells from amniotic fluid, identifying tissue-specific stem cells, and culturing them to form organoids such as lungs, intestines, and kidneys. These organoids show similar functions and gene expressions to the corresponding organs.

In a study comparing organoids from infants with congenital diaphragmatic hernia to healthy infants, researchers found that treatments could be monitored at the cellular level. This breakthrough enables more information for parents during early pregnancy and expands research in fetal development beyond legal limitations.

Gerli emphasizes the potential of organoids in studying human development and advancing prenatal medicine. This innovation opens up a new field of research that was previously limited due to legal restrictions on fetal sampling.

The future of personalized therapy for babies in the womb looks promising with the use of organoids in medical research and fetal diagnosis.

Source: www.sciencefocus.com