*Result*: Compartment-specific transcriptome of motor neurons reveals impaired extracellular matrix signaling and activated cell cycle kinases in FUS-ALS.

Title:
Compartment-specific transcriptome of motor neurons reveals impaired extracellular matrix signaling and activated cell cycle kinases in FUS-ALS.
Authors:
Zimyanin V; Department of Molecular Physiology and Biological Physics, School of Medicine, University of Virginia, Charlottesville, VA 22903, USA; Center for Membrane and Cell Physiology, School of Medicine, University of Virginia, Charlottesville, VA 22903, USA; German Center for Neurodegenerative Diseases (DZNE) Rostock/Greifswald, 18147 Rostock, Germany; Center for Transdisciplinary Neurosciences Rostock (CTNR), University Medical Center Rostock, Rostock, Germany. Electronic address: vlz3f@virginia.edu., Dash BP; Translational Neurodegeneration Section 'Albrecht Kossel', Department of Neurology, University Medical Centre Rostock, University of Rostock, Rostock, Germany. Electronic address: banaja.dash@med.uni-rostock.de., Simolka T; Translational Neurodegeneration Section 'Albrecht Kossel', Department of Neurology, University Medical Centre Rostock, University of Rostock, Rostock, Germany. Electronic address: theresasimolka@gmail.com., Glaß H; Translational Neurodegeneration Section 'Albrecht Kossel', Department of Neurology, University Medical Centre Rostock, University of Rostock, Rostock, Germany. Electronic address: hannes.glass@med.uni-rostock.de., Pal A; Dresden High Magnetic Field Laboratory (HLD-EMFL), Helmholtz-Zentrum Dresden-Rossendorf (HZDR), D-01328 Dresden, Germany. Electronic address: a.pal@hzdr.de., Haidle F; University of Würzburg, Theodor Boveri Institute, Department of Bioinformatics II, Am Hubland, 97074 Würzburg, Germany. Electronic address: felix.haidle@uni-wuerzburg.de., Zarnack K; University of Würzburg, Theodor Boveri Institute, Department of Bioinformatics II, Am Hubland, 97074 Würzburg, Germany. Electronic address: kathi.zarnack@uni-wuerzburg.de., Verma R; Department of Biology, Graduate School of Arts and Sciences, University of Virginia, Charlottesville, VA 22902, USA. Electronic address: rv6bj@virginia.edu., Khatri V; Department of Biology, Graduate School of Arts and Sciences, University of Virginia, Charlottesville, VA 22902, USA; College of Dental Medicine, Columbia University, New York, NY 10032, USA. Electronic address: vnk3zq@virginia.edu., Deppmann C; Department of Biology, Graduate School of Arts and Sciences, University of Virginia, Charlottesville, VA 22902, USA. Electronic address: deppmann@virginia.edu., Zunder E; Department of Biomedical Engineering, School of Medicine, University of Virginia, Charlottesville, VA 22902, USA. Electronic address: ezunder@virginia.edu., Müller-McNicoll M; Goethe University Frankfurt, Institute for Molecular Biosciences, Max-von-Laue-Str. 13, 60438 Frankfurt am Main, Germany. Electronic address: Mueller-McNicoll@bio.uni-frankfurt.de., Redemann S; Department of Molecular Physiology and Biological Physics, School of Medicine, University of Virginia, Charlottesville, VA 22903, USA; Center for Membrane and Cell Physiology, School of Medicine, University of Virginia, Charlottesville, VA 22903, USA; Department of Cell Biology, School of Medicine, University of Virginia, Charlottesville, VA 22903, USA. Electronic address: sz5j@virginia.edu., Hermann A; Translational Neurodegeneration Section 'Albrecht Kossel', Department of Neurology, University Medical Centre Rostock, University of Rostock, Rostock, Germany; German Center for Neurodegenerative Diseases (DZNE) Rostock/Greifswald, 18147 Rostock, Germany; Center for Transdisciplinary Neurosciences Rostock (CTNR), University Medical Center Rostock, Rostock, Germany. Electronic address: andreas.hermann@med.uni-rostock.de.
Source:
Neurobiology of disease [Neurobiol Dis] 2026 Feb; Vol. 219, pp. 107268. Date of Electronic Publication: 2026 Jan 10.
Publication Type:
Journal Article
Language:
English
Journal Info:
Publisher: Academic Press Country of Publication: United States NLM ID: 9500169 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-953X (Electronic) Linking ISSN: 09699961 NLM ISO Abbreviation: Neurobiol Dis Subsets: MEDLINE
Imprint Name(s):
Publication: San Diego, CA : Academic Press
Original Publication: Oxford : Blackwell Science, c1994-
Contributed Indexing:
Keywords: Amyotrophic lateral sclerosis; Axon degeneration; Axonal outgrowth; Axonal transcriptome; Cell cycle; DNA damage, PLK1; ECM; Induced pluripotent stem cells; RNA sequencing
Substance Nomenclature:
0 (RNA-Binding Protein FUS)
0 (Cell Cycle Proteins)
0 (FUS protein, human)
Entry Date(s):
Date Created: 20260112 Date Completed: 20260201 Latest Revision: 20260201
Update Code:
20260202
DOI:
10.1016/j.nbd.2026.107268
PMID:
41525886
Database:
MEDLINE

*Further Information*

*Mutations in FUSED IN SARCOMA (FUS) cause juvenile-onset amyotrophic lateral sclerosis (ALS). Early pathogenesis of FUS-ALS involves impaired transcription and splicing, DNA damage response, and axonal degeneration. However, the molecular pathophysiology and the link between somatic and axonal phenotypes are still poorly understood. We evaluated whether compartment-specific transcriptome differences could distinguish and drive early axonal degeneration. We used iPSC-derived motor neurons (MNs) coupled with microfluidic approaches to generate RNA-sequencing profiles from axonal and somatodendritic compartments. We demonstrate that the axonal transcriptome is unique and distinct, with RNA metabolism, extracellular secretion, and matrix disassembly pathways particularly enriched in distal axonal compartments. FUS mutation leads to changes in distinct pathways that were clustered in only a few distinct protein-protein interaction (PPI) networks. Somatodendritic changes upon FUS mutation include WNT signaling, mitochondrial, extracellular matrix (ECM)-, and synapse-related functions. In contrast, analysis of the axonal transcriptome in mutant MNs centers on the PLK1 pathway, mitochondrial gene expression, and regulation of inflammation. Comparison to CLIP-seq data revealed a significant enrichment for PLK1 and DNA replication pathways in axons. PLK1 upregulation did not activate cell-cycle re-entry but contributed to mutant MNs survival, and its inhibition increased neuronal cell death. We propose that upregulation of PLK1 represents an early event in the pathogenesis of ALS and could act in response to DNA damage, mitochondrial damage, and immune response activation in the affected cells. Additionally, downregulation of ECM pathways in the somatodendritic compartment and axons could explain strongly compromised dynamics of axonal outgrowth. Overall, we provide a novel valuable resource of the potential targets and affected processes changed in the specific compartments of FUS-ALS motor neurons.
(Copyright © 2026 The Authors. Published by Elsevier Inc. All rights reserved.)*

*Declaration of competing interest The authors declare no conflict of interest.*