Exploring PIEZO1 DNA methylation in infants with neurodevelopmental disorders

TL;DR

This study explores DNA methylation patterns of the PIEZO1 gene in infants with neurodevelopmental disorders, suggesting hypomethylation may contribute to brain development issues.

Contribution

The study is the first to investigate PIEZO1 DNA methylation in infants with neurodevelopmental disorders, identifying potential epigenetic markers.

Findings

Hypomethylation of PIEZO1 was observed in infants with neurodevelopmental disorders compared to typically developing infants.

Principal component analysis revealed distinct methylation patterns at specific CpG sites in the PIEZO1 gene.

Altered PIEZO1 methylation may impact brain tissue mechanical properties and contribute to neurodevelopmental disorders.

Abstract

Neurodevelopmental disorders (NDs) are a range of heterogeneous clinical conditions associated with dysfunctional brain development. Variations in DNA methylation (DNAm) have been reported in patients with NDs. Piezo1, which is encoded by the PIEZO1 gene, is a mechanosensitive ion channel protein involved in mechanotransduction across many physiological systems. Its regulation is involved in several diseases of the Central Nervous System (CNS) during adulthood and aging. Although PIEZO1 gene expression is susceptible to epigenetic regulation associated with pathological phenotypes during development, no previous study has explored PIEZO1 DNAm in infants with NDs.

PIEZO1 methylation in 15 CpG sites was assessed in 24 infants with NDs and in 22 infants with typical development (TD) aged between 3 and 36 months.

A principal component analysis (PCA) was run and yielded two factors: principal component1 (PC1) comprising 7 CpG sites and principal component2 (PC2) comprising 8 CpG sites. In PC2, DNAm levels were lower in infants with NDs compared to TD, suggesting hypomethylation in the clinical group, which, in turn, might impact the degree of Piezo1 protein expression.

We speculate that PIEZO1 hypomethylation as a potential epigenetic mark could contribute to the poorer mechanical properties of brain tissue in infants with NDs by altering the Piezo1 expression patterns. These findings suggest that the PIEZO1 DNAm status could serve as an early epigenetic marker of NDs, offering promising implications for identifying underlying mechanisms involved in their onset.

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