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A fluid biomarker reveals loss of TDP-43 splicing repression in pre-symptomatic ALS

Irwin, K. E.; Jasin, P.; Braunstein, K. E.; Sinha, I.; Bowden, K. D.; Moghekar, A.; Oh, E. S.; Raitcheva, D.; Bartlett, D.; Berry, J. D.; Traynor, B.; Ling, J. P.; Wong, P. C.

2023-01-24 molecular biology
10.1101/2023.01.23.525202 bioRxiv
Show abstract

Loss of TAR DNA-binding protein 43 kDa (TDP-43) splicing repression is well-documented in postmortem tissues of amyotrophic lateral sclerosis (ALS), yet whether this abnormality occurs during early-stage disease remains unresolved. Cryptic exon inclusion reflects functional loss of TDP-43, and thus detection of cryptic exon-encoded peptides in cerebrospinal fluid (CSF) could reveal the earliest stages of TDP-43 dysregulation in patients. Here, we use a newly characterized monoclonal antibody specific to a TDP-43-dependent cryptic epitope (encoded by the cryptic exon found in HDGFL2) to show that loss of TDP-43 splicing repression occurs in C9ORF72-associated ALS, including pre-symptomatic mutation carriers. In contrast to neurofilament light and heavy chain proteins, cryptic HDGFL2 accumulates in CSF at higher levels during early stages of disease. Our findings indicate that loss of TDP-43 splicing repression occurs early in disease progression, even pre-symptomatically, and that detection of HDGFL2s cryptic neoepitope may serve as a prognostic test for ALS which should facilitate patient recruitment and measurement of target engagement in clinical trials.

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