Title: Genetic foundation for complete mutant allele-specific CRISPR in neurodegenerative diseases Many cases of dominant neurodegenerative disorders defy the development of effective treatments despite their long-known genetic causes and numerous implicated underlying pathways, reflecting difficulty in defining rational drug targets through investigations focusing on mechanisms. Alternatively, development and maturation of gene targeting/lowering approaches have highlighted the value of disease-causing mutation itself as the target of treatments. Although promising, mRNA-lowering approaches suffer from inherent limitations of requirement of repeated treatments, allele-specificity, and dosage controls. We recently developed a complete allele-specific DNA targeting strategy based on CRISPR gene editing technology using PAM-altering SNP to overcome key limitations of conventional mRNA targeting approaches. Our silencing strategy achieves perfect allele specificity by using SNP variations that create CRISPR PAM sites selectively on the mutant allele/haplotype. Importantly, our novel CRISPR gene silencing strategy targets the haplotype backbone that carries the disease-causing mutation, and therefore does not depend on the type, size, and location of the disease allele, providing broadly applicable therapeutic platforms. Here, we propose to determine therapeutic potential of PAM-Altering SNP (PAS)-based CRISPR strategies 1) to prevent the transcription or 2) to induce nonsense-mediated decay of the mutant allele in cells and animal models of Huntington's disease (HD). Briefly, we will: 1) determine whether mutant allele-specific Transcription Prevention by CRISPR (TP-CRISPR) and Nonsense-Mediated Decay by CRISPR (NMD-CRISPR) efficiently introduce knockout mutations in neuronal cells derived from patients and brains of animal models of HD, 2) test whether selective silencing of mutant allele of a developmentally important gene (i.e., HTT) influences neuronal differentiation capability of induced pluripotent stem cells (iPSC), 3) compare targeting efficiency in neurons and glia, and 4) determine molecular/cellular, behavioral consequences, and pre-clinical therapeutic efficacy of mutant allele-specific CRISPR in vivo. We anticipate this research will 1) nominate optimal CRISPR targeting sites and strategies for HD, 2) generate knowledge base regarding efficiency of mutant-specific CRISPR, and 3) evaluate potential of PAS-based allele-specific CRISPR as therapeutic intervention for HD, providing 1) genetic foundation for novel and innovative therapeutic routes for HD and 2) proof-of-concept for other dominant neurodegenerative diseases.

Public Health Relevance

Genetic mutations in certain genes significantly increase the risk for or cause diseases; many of them generate adverse impacts on nervous system in a dominant fashion, resulting in devastation in affected individuals and their family members. We recently developed complete mutant allele-specific CRISPR gene silencing strategies capitalizing on PAM-altering SNPs in order to selectively target the mutation-harboring haplotype (not the mutation itself) and to provide a flexible means to inactivate any disease-causing mutation specifically and permanently. This research project aims at evaluating our promising allele-specific CRISPR DNA targeting strategy using cell and animal models of Huntington's disease as a model system, focusing on determining allele specificity, targeting efficiency, and cellular/molecular/behavioral outcomes to provide knowledge regarding silencing strategies, optimal targets for therapeutic CRISPR treatments, experimental resources, and eventually genetic foundation for precision CRISPR medicine for HD.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS105709-03
Application #
9971598
Study Section
Therapeutic Approaches to Genetic Diseases Study Section (TAG)
Program Officer
Miller, Daniel L
Project Start
2018-09-15
Project End
2023-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114