In:
PLOS ONE, Public Library of Science (PLoS), Vol. 18, No. 3 ( 2023-3-9), p. e0282822-
Abstract:
A common cause of frontotemporal dementia (FTD) are nonsense mutations in the progranulin (GRN) gene. Because nonsense mutations activate the nonsense-mediated RNA decay (NMD) pathway, we sought to inhibit this RNA turnover pathway as a means to increase progranulin levels. Using a knock-in mouse model harboring a common patient mutation, we tested whether either pharmacological or genetic inhibition of NMD upregulates progranulin in these Grn R493X mice. We first examined antisense oligonucleotides (ASOs) targeting an exonic region in Grn R493X mRNA predicted to block its degradation by NMD. As we previously reported, these ASOs effectively increased Grn R493X mRNA levels in fibroblasts in vitro . However, following CNS delivery, we found that none of the 8 ASOs we tested increased Grn mRNA levels in the brains of Grn R493X mice. This result was obtained despite broad ASO distribution in the brain. An ASO targeting a different mRNA was effective when administered in parallel to wild-type mice. As an independent approach to inhibit NMD, we examined the effect of loss of an NMD factor not required for embryonic viability: UPF3b. We found that while Upf3b deletion effectively perturbed NMD, it did not increase Grn mRNA levels in Grn +/R493X mouse brains. Together, our results suggest that the NMD-inhibition approaches that we used are likely not viable for increasing progranulin levels in individuals with FTD caused by nonsense GRN mutations. Thus, alternative approaches should be pursued.
Type of Medium:
Online Resource
ISSN:
1932-6203
DOI:
10.1371/journal.pone.0282822
DOI:
10.1371/journal.pone.0282822.g001
DOI:
10.1371/journal.pone.0282822.g002
DOI:
10.1371/journal.pone.0282822.g003
DOI:
10.1371/journal.pone.0282822.s001
DOI:
10.1371/journal.pone.0282822.s002
DOI:
10.1371/journal.pone.0282822.s003
DOI:
10.1371/journal.pone.0282822.s004
DOI:
10.1371/journal.pone.0282822.s005
Language:
English
Publisher:
Public Library of Science (PLoS)
Publication Date:
2023
detail.hit.zdb_id:
2267670-3
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