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WASHINGTON: Although the brain is thought to regulate sleep-how much, when, and how much sleep occurs-sleep deprivation affects the body, and body signals can affect sleep. The mechanisms that the body uses to regulate sleep, on the other hand, are largely unknown.
According to a recent study published in ‘Cell Reports,’ the body regulates sleep in worms through cellular pathways that ensure optimal protein function from synthesis to breakdown.
It can be difficult to know where to begin when studying the body’s sleep regulation. The researchers from the University of Tsukuba chose an unbiased investigative technique known as forward genetic screening. To accomplish this, they first used a chemical to cause random mutations in 500 worms and then used a video-based monitoring system to identify the worms that slept much more or less than average. When they identified such worms, they looked at what mutations they had and how the mutations affected sleep.
“Using this method, we were able to identify that mutations in the sel-1 and sel-11 genes were associated with longer sleep duration,” said senior author of the study Professor Yu Hayashi, adding, “Both genes code for proteins that are part of the endoplasmic-reticulum-associated protein degradation pathway, which helps cells to get rid of proteins that are misfolded.”
The researchers also found that mutations in mars-1, which is important for protein synthesis, were associated with prolonged sleep in the worms. Moreover, although sel-1, sel-11, and mars-1 were expressed in a wide range of tissues when the researchers made the worms express normal versions of some of these genes in skin cells led to normal sleep patterns. These results indicated that protein-regulating pathways in the body are indeed important for controlling sleep.
“We were also able to identify some downstream pathways that are involved in sleep regulation by modifying the expression of proteins in the worms,” said Professor Hayashi, adding, “Furthermore, when we tested our results from worms in mice, we found that these pathways also seem to regulate sleep in mammals.”Sleep disturbances are widely considered to influence inflammation and immunity, and may contribute to diseases such as inflammatory bowel disease and arthritis. A better understanding of how sleep is regulated is thus key to disease prevention. The results of this study add to a growing body of literature on sleep regulation and are hoped to improve sleep disturbance therapies in the near future that may prevent inflammatory diseases such as arthritis.
According to a recent study published in ‘Cell Reports,’ the body regulates sleep in worms through cellular pathways that ensure optimal protein function from synthesis to breakdown.
It can be difficult to know where to begin when studying the body’s sleep regulation. The researchers from the University of Tsukuba chose an unbiased investigative technique known as forward genetic screening. To accomplish this, they first used a chemical to cause random mutations in 500 worms and then used a video-based monitoring system to identify the worms that slept much more or less than average. When they identified such worms, they looked at what mutations they had and how the mutations affected sleep.
“Using this method, we were able to identify that mutations in the sel-1 and sel-11 genes were associated with longer sleep duration,” said senior author of the study Professor Yu Hayashi, adding, “Both genes code for proteins that are part of the endoplasmic-reticulum-associated protein degradation pathway, which helps cells to get rid of proteins that are misfolded.”
The researchers also found that mutations in mars-1, which is important for protein synthesis, were associated with prolonged sleep in the worms. Moreover, although sel-1, sel-11, and mars-1 were expressed in a wide range of tissues when the researchers made the worms express normal versions of some of these genes in skin cells led to normal sleep patterns. These results indicated that protein-regulating pathways in the body are indeed important for controlling sleep.
“We were also able to identify some downstream pathways that are involved in sleep regulation by modifying the expression of proteins in the worms,” said Professor Hayashi, adding, “Furthermore, when we tested our results from worms in mice, we found that these pathways also seem to regulate sleep in mammals.”Sleep disturbances are widely considered to influence inflammation and immunity, and may contribute to diseases such as inflammatory bowel disease and arthritis. A better understanding of how sleep is regulated is thus key to disease prevention. The results of this study add to a growing body of literature on sleep regulation and are hoped to improve sleep disturbance therapies in the near future that may prevent inflammatory diseases such as arthritis.
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