Rare gene explains why some people can thrive on less sleep
05-11-2025

Rare gene explains why some people can thrive on less sleep

Falling asleep and waking up refreshed is something most of us crave. Yet some people appear to thrive on fewer hours, leaving everyone else wondering how they manage it. A new study involving a healthy older adult suggests that a rare gene mutation might be a key to needing fewer hours of sleep.

The research was led by Dr. Hao Chen from the Chinese Academy of Sciences (CAS), whose team investigated a “natural short sleeper” trait linked to a genetic variant in the SIK3 gene.

How genetics influence sleep duration

Scientists who explore patterns of rest have long recognized that people’s genetic makeup can influence how much sleep they need. This latest finding highlights how even a slight genetic tweak might reduce the time required for the brain and body to recover.

Those who qualify as short sleepers function at a normal or high level despite clocking fewer hours in bed. Researchers classify them separately from individuals suffering from insomnia, because these short sleepers typically wake up rested and show no health problems tied to exhaustion.

One older participant reported sleeping around 6.3 hours per night yet displayed sharp cognition and good health. Her genetic profile pointed to a single mutation as the possible reason for her efficient slumber.

These individuals, referred to as natural short sleepers, seem wired to operate on less rest. Specialists are intrigued by how they sail through daily life with no visible drawbacks.

Gene mutation and sleep patterns

The kinase protein produced by the SIK3 gene relays signals that influence various cellular processes. Scientists suspect that changes in kinase function might play a role in controlling how much time the body devotes to sleep.

When Dr. Chen’s team transferred this mutation to lab mice, the animals spent slightly less time resting each day. This observation hinted at a biological mechanism that could be significant across different species.

“Studying human sleep genes not only expands our knowledge regarding the sleep regulatory network, but also may bring the basic research from mouse models to clinical relevance,” noted the researchers.

Brain scans in the test mice revealed that their phosphorylation patterns changed, especially around the areas that oversee rest and wake cycles. This shift aligns with the idea that sleep is coordinated by a web of signals in the brain that might be influenced by tiny chemical tweaks.

Genetic mutations in short sleepers

Scientists have now identified at least five distinct genetic mutations linked to the natural short sleep trait. Each one affects different proteins involved in the brain’s signaling and sleep-wake rhythms, hinting at multiple pathways that might influence rest duration.

The SIK3 variant joins others such as DEC2, ADRB1, NPSR1, and GRM1, each contributing a piece to the sleep efficiency puzzle. Researchers believe that mapping these variants could eventually lead to a full blueprint of how the body regulates its need for sleep.

Treatments for sleep disorders

Researchers think there could be important applications for people who struggle with sleep disorders. Adjusting the pathways linked to this genetic variant might shorten the time needed to feel rested, although practical therapies will likely take time to refine.

Still, scientists caution that these insights do not give an excuse to slash nightly rest. They emphasize that ordinary individuals without the mutation may not reap any benefits from copying a short sleeper’s schedule.

Experts see promise in pursuing treatments that enhance the body’s own efficiency. They hope new knowledge of genetic influences will guide strategies to help those who find it difficult to get restorative rest.

Future research on short-sleep genes

Short-sleep genes have captured the imagination of specialists for years. There is strong interest in mapping out exactly how the human brain resets itself, and why some people get the same benefits in a compressed timeframe.

“These [NSS] people, all these functions our bodies are doing while we are sleeping, they can just perform at a higher level than we can,” said neuroscientist and geneticist Ying-Hui Fu, from the University of California, San Francisco (UCSF).

Scientists aim to uncover the precise factors that grant this group their resilience. Many research teams intend to investigate how broader networks of genes might interact to influence rest.

The SIK3 discovery raises big questions about what else might affect daily energy levels and long-term health.

Fascination with short sleepers is unlikely to fade soon. Unlocking the secrets of their genetics could reshape how we view rest, opening a path to solutions for chronic sleep troubles.

The study is published in the journal PNAS.

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