Neuid: A Novel Neuron‐Enriched LncRNA that Connects Epigenetic Gene Silencing to Alzheimer's Disease

The increasing evidence that non-coding RNAs can become deregulated during pathogenesis is dramatically expanding the space for drug discovery beyond the protein-coding genome. Long noncoding RNAs (lncRNAs) are emerging as key regulators of cellular function, yet most remain uncharacterized. Here, we identify a previously unstudied lncRNA, which we named Neuronal Identity (Neuid), a conserved, brain-enriched transcript expressed in neurons. Neuid is downregulated in the brains of Alzheimer's disease (AD) patients. Mechanistically, Neuid maintains neuronal identity by repressing developmental and glial genes via interaction with the PRC2 subunit EZH2 and regulation of H3K27me3. Knockdown of Neuid disrupts this repression, leading to impaired neuronal activity and memory formation. Importantly, CRISPRa-mediated Neuid overexpression restores neuronal function in Aβ42-treated neurons. These findings identify NeuID as a critical regulator of neuronal plasticity and position it as a promising therapeutic target for AD.

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Publication Details

Journal
Advanced Science
Published
2026-03-14
DOI
https://doi.org/10.1002/advs.202514972
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
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article

Neuid: A Novel Neuron‐Enriched LncRNA that Connects Epigenetic Gene Silencing to Alzheimer's Disease

Verena Gisa, T. Peter Stein, Farahnaz Sananbenesi, Ivana Delalle et al.
Advanced Science
Cancer-related molecular mechanisms research
article

Neuid: A Novel Neuron‐Enriched LncRNA that Connects Epigenetic Gene Silencing to Alzheimer's Disease

Verena Gisa, T. Peter Stein, Farahnaz Sananbenesi, Ivana Delalle, Ranjit Pradhan, Sophie Schröder, Iga Grządzielewska, Zorica D. Petrović, D. Krüger, K. Toischer, Anna‐Lena Schütz, Jan Krzysztof Blusztajn, Tonatiuh Peña, Andre Fischer, Jelena Radulovic, M. Sadman Sakib, Susanne Burkhardt, Eren Diniz
article en

Abstract

The increasing evidence that non-coding RNAs can become deregulated during pathogenesis is dramatically expanding the space for drug discovery beyond the protein-coding genome. Long noncoding RNAs (lncRNAs) are emerging as key regulators of cellular function, yet most remain uncharacterized. Here, we identify a previously unstudied lncRNA, which we named Neuronal Identity (Neuid), a conserved, brain-enriched transcript expressed in neurons. Neuid is downregulated in the brains of Alzheimer's disease (AD) patients. Mechanistically, Neuid maintains neuronal identity by repressing developmental and glial genes via interaction with the PRC2 subunit EZH2 and regulation of H3K27me3. Knockdown of Neuid disrupts this repression, leading to impaired neuronal activity and memory formation. Importantly, CRISPRa-mediated Neuid overexpression restores neuronal function in Aβ42-treated neurons. These findings identify NeuID as a critical regulator of neuronal plasticity and position it as a promising therapeutic target for AD.

Advanced Science
Boston University (US), Albert Einstein College of Medicine (US), Aarhus University (DK), German Center for Neurodegenerative Diseases (DE), VA Boston Healthcare System (US), Nanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103 (DE), University of Göttingen (DE)
Good health and well-being
Openalex Percentile: Top 22%
Cancer-related molecular mechanisms research
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