Ciencia básica y patogénesis

Neurodegenerative diseases like Alzheimer's disease (AD) and prodromal stages such as Mild Cognitive Impairment involve dysregulated RNA processing. RNA methylation, a post-transcriptional RNA modification, is an important regulator of RNA stability, processing, and transport, and is mediated by RNA-binding proteins known as writers, readers, and erasers. 5-methylcytosine (m⁵C) is abundant in brain mRNAs, tRNAs, rRNAs and mt-RNA, and influences ribosomal activity and translational dynamics.

We examined if changes in the m⁵C RNA methylation system could contribute to neurodegenerative disorders. Human brain RNA-seq data from the Aging, Dementia, and Traumatic Brain Injury (TBI) Study were used to compare m⁵C effector protein expression between AD patients, TBI individuals, and age-matched controls, and correlated with AD neuropathological scores, Braak and CERAD stages. Furthermore, we assessed abundance of NSUN5, a m⁵C rRNA methyltransferase, by using confocal microscopy and brain tissue from individuals with MCI and healthy controls across different cell populations.

Altered expression of m⁵C writers (NSUN6 and NSUN7) and reader (ALYREF) protein transcripts was observed in AD and TBI across different brain regions. NSUN6 expression was found significantly reduced in the superior temporal gyrus (STG) and white matter, while NSUN7 showed increased expression in the hippocampus, correlating with Braak and CERAD stages. TBI tissue also exhibited reduced NSUN6 expression in the STGs, regardless of AD diagnosis. ALYREF showed significant differences in relative expression across Braak stages in the hippocampus and inferior parietal lobe. NSUN5 protein abundance in the human frontal gyrus was higher in pyramidal cells than glial cells overall, and significantly higher in healthy controls compared to MCI tissue.

These findings indicate consistent alterations in transcript expression of the m⁵C RNA methylation machinery in neurocognitive disorders. Our findings are consistent with evidence that mutations of m⁵C effector genes cause neurodevelopmental disorders, directly linking m⁵C and its regulator machinery with neurological processes. Evidence suggests that m⁵C effector proteins might play diverse roles, localizing to compartments such as synaptic processes. As m⁵C modifications regulate synaptic function, mitochondrial metabolism and neuronal health, they are promising novel targets for therapeutic intervention and biomarker development in cognitive diseases.