A role for the cholinergic neuron circadian clock in RNA metabolism and mediating neurodegeneration
Year: 2025
Type: article
Abstract: Circadian clocks are encoded by a transcription-translation feedback loop that aligns physiological processes with the solar cycle. Previous work linking the circadian clock to the regulation of RNA-binding proteins (RBPs) provides a foundation for the vital examination of their mechanistic connections in the context of amyotrophic lateral sclerosis (ALS)-a fatal neurodegenerative disease commonly marked by disrupted RBP function. Here, we reveal that the spinal cord cholinergic neuron rhythmic transcriptome is enriched for genes associated with ALS and other neurodegenerative diseases. We show that there is time-of-day-dependent expression of ALS-linked RBP transcripts and rhythmic alternative splicing of genes involved in microtubule cytoskeleton organization, intracellular trafficking, and synaptic function. Through in silico analysis of RNA sequencing data from sporadic ALS patients, we find that gene expression profiles altered in disease correspond with rhythmic gene networks. Finally, we report that clock disruption through cholinergic neuron-specific deletion of clock activator BMAL1 increases neurodegeneration and drives time-of-day-dependent alternative splicing of RNA processing genes. Our results establish a role for the cholinergic neuron circadian clock in RNA metabolism and mediating neurodegeneration.
Source: Life Science Alliance
Authors: Sharon B Tam, Nathan J Waldeck, Matthew Wright, Jelena Mojsilovic-Petrovic, Erin M Baker, Evangelos Kiskinis, Joseph Bass, Robert G Kalb
Institution: Northwestern University
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,500
Awards: G1284175734, G1382277591, G1697802790, G317886719, G4119534169, SUPPRESSION OF TDP-43 PROTEINOPATHY IN MICE BY TARGETING RAD-23, G5850682332, G6544658276, G9000046704, G9000094325, G9000243610, RAD23 Control of ALS phenotypes, The Robert H. Lurie Comprehensive Cancer Center, Defining mechanisms underlying C9orf72-associated frontotemporal dementia with C. elegans and mammalian models
OpenAlex ID: W4417345529
