York researchers publish novel findings on role of tumor suppressor protein in muscle health

research microscope

Researchers out of the Faculty of Health have published novel findings addressing a long-running debate about the role of the tumor suppressor protein p53 in muscle metabolic health.

Ashley Oliviera
Ashley Oliviera
David Hood
David Hood
Jonathan Memme
Jonathan Memme

In a study published in the Journal of Biological Chemistry, Jonathan Memme, lead author, PhD student in Kinesiology and Health Science (KAHS), Ashley Oliveira, contributing author, PhD student in KAHS, and David A. Hood, senior author, professor and Tier I Canada Research Chair, and director of the Muscle Health Research Centre (MHRC), show that the importance of p53 is most evident under stress conditions where the maintenance of mitochondrial function is essential.

Since its discovery in the late 1990s, p53 has been a focal point of research and lauded for its role in regulating the metabolic programming of the cell. While p53 is often studied in the context of cancer as a potent tumor suppressor protein, researchers in the MHRC have focused on understanding how p53 regulates mitochondria in muscle, the organelles responsible for providing energy to muscle cells.

“The contribution of mitochondria to the metabolic health of skeletal muscle is of widespread interest, with implications that extend to not only fitness, but also to healthy aging and the prevention of various diseases,” said Memme.

Previous research has indicated that p53 plays a role in mediating the mechanisms that regulate mitochondrial quality in muscle, such as synthesis of new mitochondria (termed biogenesis), as well as elimination of dysfunctional mitochondria that may become toxic to the cell. However, the degree to which p53 is essential to regulating these mitochondrial adaptations, to this point, has remained controversial. Until now, there have been no studies that examine the role of p53 under conditions of chronic muscle disuse in which mitochondrial dysfunction is evident as part of the atrophy and muscle weakening process.

In this study, York researchers set out to determine the necessity of p53 in maintaining mitochondrial content and function in muscle, both basally as well as following acute and chronic muscle disuse. Using RNA-sequencing technology, among other biochemical assessments of mitochondrial content and function, researchers assessed the effect of p53 ablation from muscle on more than 20,000 genes.

The inquiry led to convincing evidence to suggest that p53 is perhaps not required for basal maintenance of mitochondrial health in muscle; however, under stress conditions such as with chronic disuse, the absence of p53 contributes to exacerbated declines in mitochondrial function brought about by defects in the mitochondrial quality control machinery, particularly mitochondrial clearance via mitophagy.

“Together, our data illustrate exacerbated mitochondrial dysregulation with denervation stress in skeletal muscle in the absence of a functional p53 protein, thus indicating that p53 contributes to organellar maintenance via regulation of MQC pathways during muscle atrophy,” said Hood.

These results address a decades-worth debate about the role of p53 in muscle metabolic health and show that the true importance of p53 is most evident under stress conditions where the maintenance of mitochondrial function is essential.