Biological clocks are an organism's innate timing device. It is composed of specific proteins called clock proteins, which interact in cells throughout the body. Biological clocks produce and regulate circadian rhythms - the physical, mental, and behavioural changes that follow a daily cycle. Understanding the molecular mechanisms of the circadian clock provides a huge potential to identify therapeutic interventions to mitigate circadian disruption, and its long-term consequences such as diabetes, obesity and cancer among shift workers, who undergo frequent circadian disruption and are more prone to these diseases.
The Duke-NUS scientists had previously discovered that mutations in a specific protein (called casein kinase 1) alters the core clock protein (called PERIOD or PER), and this changes the timing of the biological clock. In this study, preclinical models were used to investigate the role of PER2 (a type of PER protein) in clock regulation to further understand and strengthen the model.
"The study findings clearly demonstrated that targeted mutations in the PER2 protein can alter the balance of biological clock and can significantly lengthen the circadian period in preclinical models," said Dr Rajesh Narasimamurthy, Principal Research Scientist at the Duke-NUS' Cancer and Stem Cell Biology (CSCB) programme.
"People's sleep/wake patterns play a significant role in determining their cognitive skills, social behavior and their responses to drug," said Professor David Virshup, Director of the Duke-NUS' CSCB programme and corresponding author of this study.
"Our study helps us understand and validate the genetic and biochemical regulation of our circadian sleep/wake cycles, which can produce a morning lark or night owl effect. Understanding how the clock works can help in the development of new therapeutic interventions for treating people with sleep disorders," Prof Virshup added.
"Sleep disorders are increasingly recognised as a major public health concern. This important study by our researchers could open new possibilities and strategies to treat sleep disorders, and improve the quality of life among affected individuals in Singapore and beyond," said Professor Patrick Casey, Senior Vice Dean for Research at Duke-NUS.
The team is currently investigating other factors that can cause mutation in PER2 protein and regulate the clock speed.
Reference: Masuda, S., Narasimamurthy, R., Yoshitane, H., Kim, J. K., Fukada, Y., & Virshup, D. M. (2020). Mutation of a PER2 phosphodegron perturbs the circadian phosphoswitch. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.2000266117
This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.