DCPS modulates TDP-43-linked neurodegeneration through P-body-mediated RNA decay

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Authors: Yingzhi Ye, Zhe Zhang, Yu Xiao, Chengzhang Zhu, Noelle Wright, J Asbury, Yongxin Huang, Wei Wang, Laura Gómez-Isaza, Juan C. Troncoso, Chuan He, Shuying Sun
Cited by: 3
References: 98

Abstract

The proteinopathy of the RNA-binding protein TDP-43, characterized by nuclear clearance and cytoplasmic inclusion, is a hallmark of multiple neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), and Alzheimer's disease (AD). Through CRISPR interference (CRISPRi) screening in human neurons, we identified the decapping scavenger enzyme (DCPS) as a novel genetic modifier of TDP-43 loss-of-function (LOF)-mediated neurotoxicity. Our findings reveal that TDP-43 LOF leads to aberrant mRNA degradation via dysregulating the properties and activity of processing bodies (P-bodies). TDP-43 interacts with P-body component proteins, potentially influencing their dynamic equilibrium and assembly into ribonucleoprotein (RNP) granules. Loss of TDP-43 hyperactivates P-bodies, increasing mRNA association and RNA decay. Reducing DCPS restores P-body integrity and RNA turnover, ultimately improving neuronal survival. Overall, this study highlights a novel role of TDP-43 in RNA processing through P-body regulation and identifies DCPS as a potential therapeutic target for TDP-43 proteinopathy-related neurodegenerative diseases.

Fields of Study & Subjects

Amyotrophic Lateral Sclerosis Research Neurogenesis and neuroplasticity mechanisms Genetic Neurodegenerative Diseases

Publication details

Journal / source
Neuron
Publisher
Elsevier BV
Volume
114
Issue
11
Pages
1970–1985.e12
Publication date
9 March 2026
Language
EN