Alterations in RNA editing in skeletal muscle following exercise training in individuals with Parkinson's disease.
Heather Milliken MercerAiswarya Mukundan NairAngela RidgelHelen PiontkivskaPublished in: PloS one (2023)
Parkinson's Disease (PD) is the second most common neurodegenerative disease behind Alzheimer's Disease, currently affecting more than 10 million people worldwide and 1.5 times more males than females. The progression of PD results in the loss of function due to neurodegeneration and neuroinflammation. The etiology of PD is multifactorial, including both genetic and environmental origins. Here we explored changes in RNA editing, specifically editing through the actions of the Adenosine Deaminases Acting on RNA (ADARs), in the progression of PD. Analysis of ADAR editing of skeletal muscle transcriptomes from PD patients and controls, including those that engaged in a rehabilitative exercise training program revealed significant differences in ADAR editing patterns based on age, disease status, and following rehabilitative exercise. Further, deleterious editing events in protein coding regions were identified in multiple genes with known associations to PD pathogenesis. Our findings of differential ADAR editing complement findings of changes in transcriptional networks identified by a recent study and offer insights into dynamic ADAR editing changes associated with PD pathogenesis.
Keyphrases
- crispr cas
- skeletal muscle
- end stage renal disease
- genome wide
- chronic kidney disease
- physical activity
- traumatic brain injury
- dna methylation
- metabolic syndrome
- adipose tissue
- risk assessment
- body composition
- oxidative stress
- peritoneal dialysis
- mild cognitive impairment
- lipopolysaccharide induced
- prognostic factors
- human health
- subarachnoid hemorrhage
- protein kinase
- bioinformatics analysis