Brain : a journal of neurologyOct 5, 2026

Gene editing screen shows FTO’s m6A modification of ATF3 may protect against stroke damage

CRISPR Gene Editing Weekly Brief ↗PubMed ↗DOI ↗

Updated Oct 6, 2026

Abstract

Fto expression was progressively reduced while global m6A levels increased during ischaemic injury.

Fto was identified as a top negatively selected gene in neuronal cells under oxygen-glucose deprivation/reoxygenation.
Neuron-specific knockout of Fto led to increased infarct size, neurological deficits, cognitive impairment, and neuronal cell death.
RNA sequencing analysis indicated the activation of multiple signaling pathways associated with Fto deficiency.
Atf3 was found to be hypermethylated and upregulated downstream of Fto loss, linking m6A dysregulation to higher neuronal apoptosis.
Knockdown of Fto increased ATF3 mRNA methylation and expression, while Fto overexpression mitigated brain injury and improved neurological outcomes.

Simplified

RNA modifications, especially N6-methyladenosine (m6A), have emerged as pivotal regulators of gene expression in neurological disorders, yet their roles in ischaemic stroke remain unclear. Here, we performed a CRISPR-Cas9 loss-of-function screen targeting 118 RNA modification-related genes in neuronal cells subjected to oxygen-glucose deprivation/reoxygenation (OGD/R) and validated the findings in a mouse model of middle cerebral artery occlusion/reperfusion (MCAO/R). We identified Fto as a top negatively selected gene, with its expression progressively reduced and global m6A levels increased during ischaemic injury. Neuron-specific Fto knockout aggravated infarct size, neurological deficits, cognitive impairment, and neuronal apoptosis, accompanied by activation of multiple signalling pathways revealed by RNA-seq analysis. Integrated m6A-seq and RNA-seq profiling uncovered Atf3 as a hypermethylated and upregulated hub gene downstream of Fto deficiency, linking m6A dysregulation to enhanced neuronal apoptosis. In vitro assays confirmed that FTO knockdown increased ATF3 mRNA methylation and expression under OGD/R conditions, whereas Fto overexpression in vivo alleviated ischaemic brain injury, improved neurological outcomes, reduced Atf3 expression, and lowered global m6A levels. Together, our findings reveal the Fto/m6A/ATF3 axis as a critical mediator of ischaemic injury and highlight Fto restoration as a potential therapeutic strategy for stroke.

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Gene editing screen shows FTO’s m6A modification of ATF3 may protect against stroke damage

Abstract

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