Tuesday, December 02, 2025

 

Epigenetics linked to high-altitude adaptation in Andes



Whole methylome data gives new insights into Indigenous people of South America



Emory University





DNA sequencing technology makes it possible to explore the genome to learn how humans adapted to live in a wide range of environments. Research has shown, for instance, that Tibetans living at high altitude in the Himalayas have a unique variant of a gene that expands the oxygen-carrying capacity of their blood.

Scientists, however, have not found a strong signal for this “high-altitude gene” in the genomes of Indigenous people living in the Andes Mountains of South America. It’s been less clear how people adapted to the altitudes greater than 2,500 meters in the Andean highlands, where low-oxygen levels, frigid temperatures and intense ultraviolet radiation make life challenging in the extreme.

A study led by anthropologists at Emory University took a new approach to explore this Andean mystery.

Rather than scan the whole genome of Indigenous people to look for alterations in the genetic code, the researchers scanned the entire methylome. The methylome reveals what are called “epigenetic” changes in the genome — how genes are expressed in response to the environment through a chemical process known as DNA methylation.

The journal Environmental Epigenetics published the research, which adds to the evidence that epigenetics may play a bigger role in adaptation than previously realized.

The researchers compared the methylomes of 39 individuals from two modern-day Indigenous populations: the Kichwa from the Andean highlands of Ecuador and the Ashaninka from the lowland Amazon Basin along the Peruvian border of Ecuador.

“This is the first whole methylome data on these two populations,” says Yemko Pryor, first author of the study, who led the project as an Emory PhD student. “Unlike many methylome studies that focus on just a few hundred thousand sites throughout the genome, we looked at all three million base pairs to see what we would find.”

The results identified strong differences in DNA methylation between the low- and high-altitude populations for the PSMA8 gene, associated with regulation of the vascular system, and for the FST gene, associated with regulating muscles in the heart. 

The second strongest signal detected in the high-altitude population compared to the low-altitude population was for genes within the P13K/AKT pathway, which is associated with muscle growth and the creation of new blood vessels.

The researchers hypothesize that the interplay between these epigenetic differences may help explain the increased muscularization of small arteries and higher blood viscosity that has been found in high-altitude Andean populations. These differences, they explain, may represent a unique vascular adaptation to a low-oxygen environment distinct from those found in Tibetan populations.

And the researchers note that the P13K/AKT pathway has been implicated in arteriole wall thickening under low-oxygen conditions in rats, as well as in human cells. “Arteriole wall thickening in humans has been linked to the development of pulmonary hypertension, which is more common in Andean highlanders compared to other highland populations,” they write.

The current study also identified strong differences between the two populations in the methylation of 39 pigmentation-related genes, which may help explain adaptation by the high-altitude population to strong ultraviolet radiation.

“The findings are particularly interesting because we’re not seeing these strong signals in the genome but when we look at the methylome, we are seeing these changes,” says John Lindo, Emory associate professor of anthropology and senior author of the study.

Gene selection theory holds that a gene that helps a population to adapt over time needs to be reliably inherited and therefore would show up in the genetic code of the genome. An epigenetic change, however, represents a more flexible response to an environmental influence, which would not necessarily be passed down to offspring.

“The Kichwa population that participated in our study did not just arrive in the Andean highlands — their ancestors had been living there for nearly 10,000 years,” Lindo says. “Our findings suggest that epigenetics can contribute to adaptation in a longstanding way.”

Co-authors of the current paper include scientists from Central University of Ecuador; the Institute of Medicine and Forensic Sciences in Lima, Peru; the State University of Rio de Janeiro; and the University of Pavia in Pavia, Italy.

Lindo established the Lindo Ancient DNA Laboratory at Emory in 2020. The state-of-the-art facility is one of the handful of ancient DNA labs in the country and one of the few in the world involved in every step of the complex process of solving mysteries surround ancient remains. A focus of the lab is exploring how environmental changes — including those caused by European contact — affected the biology of Indigenous and other populations of the Americas.

“I was one of the first graduate students to join the lab,” says Pryor, who received her PhD from Emory in June. “I learned how to build a lab from the ground up while also getting hands-on analytical and technical skills.”

While much of the lab’s work centers on ancient DNA, it also spans analyses of modern-day Indigenous populations, both for comparative studies and to fill in gaps around key questions when ancient samples are lacking.

The Emory lab builds relationships with Indigenous populations and local scientists, establishing full collaborations to conduct the research and ensuring that the participating communities have access to the findings.

As part of her Emory experience, Pryor traveled to Ecuador to meet with local archaeologists and members of Indigenous communities participating in some of the lab’s research projects.

“As a scientist doing research on humans, it’s also important to go beyond the data and be in community with people,” she says. “As much as I love doing analyses in the lab, it was a beautiful experience for me to get to go into the field and engage directly with people there.”

A key component of the current paper will be workshops that the team will hold to convey their findings directly to the Kichwa and Ashaninka communities. Co-author Daniel Rivas Alava, an Emory graduate student of anthropology and a native of Ecuador, is currently developing the Kichwa workshop.

Pryor graduated from Emory in June and is now a postdoctoral fellow in the lab of Tina Lasisi at the University of Michigan, researching the evolution and genetic basis of variation in human characteristics, with a focus on pigmentation and hair.

“I’m applying many of the techniques I learned at Emory, especially computational skills,” Pryor says. “My dream is to stay in academia and start my own ancient DNA lab one day.”

Language mixing has no negative effect on toddlers’ vocabulary development, Concordia research shows



Parents in bilingual families often switch languages when talking to young children, for a variety of reasons




Concordia University

Krista Byers-Heinlein and Alexandra Paquette 

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Krista Byers-Heinlein, left, and Alexandra Paquette

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Credit: Concordia University




Parents in bilingual and multilingual families can wrestle with when and how to expose infants and toddlers to words in different languages. However, a new paper from the Concordia Infant Research Lab shows that language mixing does not harm a child’s ability to learn words.

In fact, switching languages, even mid-sentence or to introduce a single word, is considered both a common and flexible way to communicate in multilingual homes.

“We found that language mixing is often an intentional strategy rather than something parents do subconsciously,” says PhD student Alexandra Paquette, the study’s lead author. “There was no strong evidence that vocabulary size was tied to language mixing. We found that children were able to successfully navigate two languages, even when they appeared in the same sentence. Parents don’t need to worry that mixing harms their child’s ability to learn new words.”

Franglais begins at home

The study, published in the journal Behavioral Sciences, looks at data from almost 400 Montreal children being raised in bilingual homes. The Canadian metropolis benefits from a linguistically diverse population. French and English are both societal languages, meaning large portions of the population speak one or both. The city’s linguistic makeup is also enriched by its significant immigrant population, who speak multiple heritage languages. The most common are Spanish, Arabic and Italian.

The researchers analyzed two groups: French-English bilingual families and families who speak a heritage language along with English and/or French. Parents completed detailed questionnaires about how often they mixed languages, their reasons for doing so and how much of each language their child heard. They also documented their children’s understanding and use of words.

The results show that language mixing is common, but its frequency varies depending on the family’s linguistic background. French-English parents tended to mix less than heritage-language parents, likely because both societal languages are well supported in Montreal. Heritage-language parents mixed more often, especially borrowing English or French terms while speaking their heritage language.

Parents of all backgrounds said they switched languages for several reasons: they could not find the right word in English, French or their heritage language; no good translation was available; or they wanted to introduce a new word to their child. Parents in French-English families with older toddlers were more likely to deliberately mix languages to encourage language development.

The researchers point out that language mixing had almost no effect on a child’s vocabulary score in either French-English or English- or French-heritage language families. Even if parents mixed often, children knew the same number of words.

A unique linguistic environment

Montreal’s particular makeup as a city with two status languages supplemented by many heritage languages shapes how parents raise their bilingual children. Language mixing is a byproduct of a cultural context in which language mixing is common in daily life in both English and French communities.

“This project shows us how flexible children when it comes to language development,” says co-author Krista Byers-Heinlein, a professor in the Department of Psychology.

“Rather than confuse children, language mixing can be a real teaching tool that parents have in their toolbox. Parents are strategic about it, and our research finds that it is either neutral or beneficial when it comes to vocabulary.”

Read the cited paper: “Parental Language Mixing in Montreal: Rates, Predictors, and Relation to Infants’ Vocabulary Size


Ants signal deadly infection in altruistic self-sacrifice

Early disease detection in the colony: Ants signal incurable sickness to save others

Institute of Science and Technology Austria

Unpacking of a fatally-infected pupa from its cocoon 

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When an ant pupa signals its imminent death caused by an incurable infection, worker ants unpack it from its cocoon and disinfect it, leading to its demise.

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Credit: © Christopher D. Pull / ISTA





Ant colonies operate as tightly coordinated “superorganisms” with individual ants working together, much like the cells of a body, to ensure their collective health. Researchers at the Institute of Science and Technology Austria (ISTA) have now discovered that terminally ill ant brood, like infected cells, release an odor signaling their impending death and the risk they pose. This sophisticated early warning system facilitates rapid detection and removal of pathogenic infections. The study was published in Nature Communications.

In many social animals, group members try to conceal their sickness to prevent social exclusion. Ant brood, however, take the opposite approach. When facing an incurable infection, ant pupae actively emit an alarm signal that warns the colony of the contagion risk they are about to pose.

Upon receiving the signal, worker ants respond swiftly by unpacking the terminally ill pupae from their cocoon, creating small openings in their body surface and applying their antimicrobial poison, formic acid, which functions as a self-produced disinfectant. While this treatment immediately kills the pathogens multiplying inside the pupa, it also results in the pupa’s own demise.

“What appears to be self-sacrifice at first glance is, in fact, also beneficial to the signaler: it safeguards its nestmates, with whom it shares many genes. By warning the colony of their deadly infection, terminally ill ants help the colony remain healthy and produce daughter colonies, which indirectly pass on the signaler’s genes to the next generation,” explains Erika Dawson, first author of the study and former postdoc in the Social Immunity’ research group headed by Sylvia Cremer at ISTA.

Their collaborative study with chemical ecologist Thomas Schmitt from the University of Würzburg in Germany describes this altruistic disease signaling in social insects for the first time. If a fatally ill ant were to conceal its symptoms and die undetected, it could become highly infectious, endangering not only itself but the entire colony. Active signaling of the incurably infected instead allows effective disease detection and pathogen removal by the colony.

Altruistic self-sacrifice

At the colony level, ants function as a “superorganism,” effectively forming a single living entity. While one or more queens are responsible for producing offspring, the non-fertile workers take on all tasks related to colony maintenance and health. This mirrors cell specialization in the human body, where germline cells in the reproductive organs are dedicated to offspring production while somatic cells carry out all other essential functions.

In both organisms and superorganisms, reproductive and non-reproductive components are fully interdependent, with each essential for the survival of the whole. Cooperation is therefore crucial. Much like cells in our body, individual ants collaborate closely, even engaging in altruistic self-sacrifice for the benefit of the colony.

Find-me and eat-me signal

Why would a complex early warning system evolve if sick animals can simply isolate themselves from the colony? “Adult ants that approach death leave the nest to die outside the colony. Similarly, workers that have been exposed to fungal spores practice social distancing,” explains Cremer. “Yet, this is only possible for mobile individuals. Ant brood within the colony, like infected cells in tissue, are largely immobile and lack this option.”

Body cells and ant brood, such as developing pupae, both rely on external assistance to safeguard the colony. Intriguingly, both address this challenge in similar ways: they emit a chemical signal that attracts either the body’s immune cells or the colony’s workers, allowing these helpers to detect and eliminate them as potential sources of infection. Immunologists call this the “find-me and eat-me signal.”

“The signal must be both sensitive and specific,” explains Cremer. “It should help to identify all terminally-sick ant pupae but be precise enough to avoid triggering the unpacking of healthy pupae or those capable of overcoming the infection with their own immune system.” What properties must such a signal have to achieve this level of precision?

Changes in pupal scent profile

Schmitt, whose research focus is on chemical communication in social insects, explains that workers specifically target individual pupae out of the brood pile. “This means the scent cannot simply diffuse through the nest chamber but must be directly associated with the diseased pupa. Accordingly, the signal does not consist of volatile compounds but instead is made up of non-volatile compounds on the pupal body surface.”

In particular, the intensity of two odor components from the ants’ natural scent profile increases when a pupa is terminally ill. To test whether this odor change alone could trigger the workers’ disinfection behavior, the researchers transferred the signal odor to healthy pupae and observed the workers’ reaction.

“We extracted the smell from the signaling pupae and applied it to healthy brood,” Cremer says in describing the experimental approach. The results were conclusive: Transfer of the signal scent alone was sufficient to induce unpacking by the ants, revealing that the altered body odor of fatally-infected pupae serves the same function as the ‘find-me and eat-me’ signal of infected body cells.

Signaling only in uncontrollable cases

According to Dawson, the fascinating aspect is that ants do not signal infection indiscriminately. “Queen pupae, which have stronger immune defenses than worker pupae and can limit the infection on their own, were not observed to emit this warning signal to the colony,” she explains. “Worker brood, on the other hand, were unable to control the infection and signaled to alert the colony.”

By signaling only when an infection becomes uncontrollable, the sick brood enable the colony to respond proactively to real threats. At the same time, this approach ensures that individuals capable of recovery are not sacrificed unnecessarily. “This precise coordination between the individual and colony level is what makes this altruistic disease signaling so effective,” Cremer concludes.

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Information on animal studies

To better understand fundamental processes, for example in the fields of behavioral biology, immunology or genetics, the use of animals in research is indispensable. No other methods, such as in silico models, can serve as an alternative. The animals are collected, reared, and used in the experiments in accordance with strict legal regulations.