Altered mRNA transport and local translation in i3Neurons with RNA-binding protein knockdown

Neurons rely on messenger RNA (mRNA) transport and local translation to facilitate rapid protein synthesis in processes far from the cell body. These processes allow precise spatial and temporal control of translation and are mediated by RNA-binding proteins (RBPs), including those associated with neurodegenerative diseases. Here, we use proteomics, transcriptomics, and microscopy to investigate the impact of RBP depletion on mRNA transport and local translation in induced pluripotent stem cell-derived neurons. We find thousands of transcripts enriched in neurites and that many of these transcripts are locally translated, possibly due to the shorter length of transcripts in neurites. Loss of frontotemporal dementia/amyotrophic lateral sclerosis (FTD/ALS)-associated RBPs TDP-43 and hnRNPA1 induce distinct alterations in the neuritic proteome and transcriptome. TDP-43 knockdown (KD) leads to slightly increased neuritic mRNA and translation, while hnRNPA1 loss has more moderate effects on local mRNA profiles, possibly due to compensation by hnRNPA3. These results highlight the crucial role of FTD/ALS-associated RBPs in mRNA transport and local translation in neurons and the importance of these processes in neuron health and disease.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-07-19
DOI
https://doi.org/10.1093/nar/gkaf709
Citations
3
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
4.17

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article

Altered mRNA transport and local translation in i3Neurons with RNA-binding protein knockdown

Puja R. Mehta, Veronica H. Ryan, Christina N. Como, Stephanie L. Sarbanes et al.
3 citations
Nucleic Acids Research
Amyotrophic Lateral Sclerosis Research
4.17
article

Altered mRNA transport and local translation in i3Neurons with RNA-binding protein knockdown

Puja R. Mehta, Veronica H. Ryan, Christina N. Como, Stephanie L. Sarbanes, Colleen Bereda, Nicholas L. Johnson, Yue Qi, Alla Mikheenko, Matthew J. Keuss, Cory A. Weller, Ziyi Li, Ying Hao, Rachael Dargan, Emma J. Craig, Mike A. Nalls, Benjamin Packer
article en
3 citations

Abstract

Neurons rely on messenger RNA (mRNA) transport and local translation to facilitate rapid protein synthesis in processes far from the cell body. These processes allow precise spatial and temporal control of translation and are mediated by RNA-binding proteins (RBPs), including those associated with neurodegenerative diseases. Here, we use proteomics, transcriptomics, and microscopy to investigate the impact of RBP depletion on mRNA transport and local translation in induced pluripotent stem cell-derived neurons. We find thousands of transcripts enriched in neurites and that many of these transcripts are locally translated, possibly due to the shorter length of transcripts in neurites. Loss of frontotemporal dementia/amyotrophic lateral sclerosis (FTD/ALS)-associated RBPs TDP-43 and hnRNPA1 induce distinct alterations in the neuritic proteome and transcriptome. TDP-43 knockdown (KD) leads to slightly increased neuritic mRNA and translation, while hnRNPA1 loss has more moderate effects on local mRNA profiles, possibly due to compensation by hnRNPA3. These results highlight the crucial role of FTD/ALS-associated RBPs in mRNA transport and local translation in neurons and the importance of these processes in neuron health and disease.

Nucleic Acids ResearchVol. 53(14)
Queen Mary University of London (GB), The Francis Crick Institute (GB), National Institute of Neurological Disorders and Stroke (US), All Russian Research Institute of Hydrometeorological information World Data Center (RU), Institute on Aging (US), National Institute on Aging (US), University College London (GB)
U.S. Department of Health and Human Services, National Institutes of Health, National Institute on Aging, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Good health and well-being
Openalex Percentile: Top 6%
Amyotrophic Lateral Sclerosis Research
4.17
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