دورية أكاديمية

Modulation of prion protein expression through cryptic splice site manipulation.

التفاصيل البيبلوغرافية
العنوان: Modulation of prion protein expression through cryptic splice site manipulation.
المؤلفون: Gentile JE; McCance Center for Brain Health and Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Corridon TL; McCance Center for Brain Health and Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Mortberg MA; McCance Center for Brain Health and Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., D'Souza EN; Big Data Institute and Centre for Human Genetics, University of Oxford, Oxford, UK., Whiffin N; Big Data Institute and Centre for Human Genetics, University of Oxford, Oxford, UK; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Minikel EV; McCance Center for Brain Health and Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Vallabh SM; McCance Center for Brain Health and Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA. Electronic address: svallabh@broadinstitute.org.
المصدر: The Journal of biological chemistry [J Biol Chem] 2024 Aug; Vol. 300 (8), pp. 107560. Date of Electronic Publication: 2024 Jul 11.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID: 2985121R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1083-351X (Electronic) Linking ISSN: 00219258 NLM ISO Abbreviation: J Biol Chem Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : [New York, NY] : Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology
Original Publication: Baltimore, MD : American Society for Biochemistry and Molecular Biology
مواضيع طبية MeSH: Exons* , RNA Splice Sites* , Prion Proteins*/metabolism , Prion Proteins*/genetics, Humans ; RNA Splicing ; Introns ; Gene Expression Regulation ; Animals ; Prions/metabolism ; Prions/genetics ; Prion Diseases/metabolism ; Prion Diseases/genetics ; 5' Untranslated Regions
مستخلص: Lowering expression of prion protein (PrP) is a well-validated therapeutic strategy in prion disease, but additional modalities are urgently needed. In other diseases, small molecules have proven capable of modulating pre-mRNA splicing, sometimes by forcing inclusion of cryptic exons that reduce gene expression. Here, we characterize a cryptic exon located in human PRNP's sole intron and evaluate its potential to reduce PrP expression through incorporation into the 5' untranslated region. This exon is homologous to exon 2 in nonprimate species but contains a start codon that would yield an upstream open reading frame with a stop codon prior to a splice site if included in PRNP mRNA, potentially downregulating PrP expression through translational repression or nonsense-mediated decay. We establish a minigene transfection system and test a panel of splice site alterations, identifying mutants that reduce PrP expression by as much as 78%. Our findings nominate a new therapeutic target for lowering PrP.
Competing Interests: Conflict of interest S. M. V. acknowledges speaking fees from Ultragenyx, Illumina, Biogen, and Eli Lilly, consulting fees from Invitae and Alnylam, and research support from Ionis, Gate, and Sangamo. E.V.M. acknowledges speaking fees from Eli Lilly, consulting fees from Deerfield and Alnylam, and research support from Ionis, Gate, and Sangamo.
(Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)
التعليقات: Update of: bioRxiv. 2023 Dec 19:2023.12.19.572439. doi: 10.1101/2023.12.19.572439. (PMID: 38187635)
معلومات مُعتمدة: United Kingdom WT_ Wellcome Trust; R01 NS125255 United States NS NINDS NIH HHS
فهرسة مساهمة: Keywords: cryptic exon; minigene; prion protein; splice modulation; upstream open reading frame
المشرفين على المادة: 0 (RNA Splice Sites)
0 (Prion Proteins)
0 (PRNP protein, human)
0 (Prions)
0 (5' Untranslated Regions)
تواريخ الأحداث: Date Created: 20240713 Date Completed: 20240904 Latest Revision: 20240904
رمز التحديث: 20240904
مُعرف محوري في PubMed: PMC11342779
DOI: 10.1016/j.jbc.2024.107560
PMID: 39002681
قاعدة البيانات: MEDLINE
الوصف
تدمد:1083-351X
DOI:10.1016/j.jbc.2024.107560