Cryptic inclusions UNCover losses driving neurodegeneration
- PMID: 35773026
- DOI: 10.1016/j.tig.2022.06.004
Cryptic inclusions UNCover losses driving neurodegeneration
Abstract
Pathology formed by the protein TDP-43 (TAR DNA binding protein 43) is the hallmark of several neurodegenerative diseases. Recent studies by Ma et al. and Brown et al. reveal that loss of TDP-43 function causes inclusion of cryptic exons in specific mRNAs, including the synaptic gene UNC13A, a known genetic risk factor for amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). These findings suggest new disease mechanisms.
Keywords: TDP-43; amyotrophic lateral sclerosis; cryptic exons; frontotemporal dementia; motor neuron; splicing.
Copyright © 2022 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests No interests are declared.
Comment on
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TDP-43 represses cryptic exon inclusion in the FTD-ALS gene UNC13A.Nature. 2022 Mar;603(7899):124-130. doi: 10.1038/s41586-022-04424-7. Epub 2022 Feb 23. Nature. 2022. PMID: 35197626 Free PMC article.
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TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A.Nature. 2022 Mar;603(7899):131-137. doi: 10.1038/s41586-022-04436-3. Epub 2022 Feb 23. Nature. 2022. PMID: 35197628 Free PMC article.
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