The deletion of mutant SOD1 via CRISPR/Cas9/sgRNA prolongs survival in an amyotrophic lateral sclerosis mouse model.

Abstract

The superoxide dismutase 1 (SOD1) mutation is one of the most notable causes of amyotrophic lateral sclerosis (ALS), and modifying the mutant SOD1 gene is the best approach for the treatment of patients with ALS linked to the mutations in this gene. Clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated (Cas9)/sgRNA delivered by the adeno-associated virus (AAV) system is a powerful tool for genome editing in the central nervous system (CNS). Here, we tested the capacity of the AAV-SaCas9-sgRNA system to modify mutant SOD1 in SOD1G93A transgenic mice and found that AAV9-SaCas9-sgRNA5 deleted the SOD1 gene, improved the lifespan of SOD1G93A mice by 54.6%, and notably ameliorated the performance of ALS transgenic mice. An immunochemical analysis showed that the expression of mutant SOD1 was very weak in motor neurons expressing SaCas9-sgRNA5. Consequently, the area showing muscle atrophy was more notably restored in the group treated with SaCas9-sgRNA5 compared with the group treated with SaCas9-sgLacZ. In addition, deep sequencing did not show the indel mutation in the gene highly matched to sgRNA5. Hence, AAV9-SaCas9-sgRNA-based gene editing is a feasible potential treatment for patients with ALS linked to SOD1 mutations.

• Authors: Weisong Duan, Moran Guo, Le Yi, Yakun Liu, Zhongyao Li, Yanqin Ma, Guisen Zhang, Yaling Liu, Hui Bu, Xueqin Song, Chunyan Li
• Journal: Gene therapy (Gene Ther) Vol. 27 Issue 3-4 Pg. 157-169 (04 2020) ISSN: 1476-5462 [Electronic] England
• PMID: 31819203 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• RNA, Guide
• Sod1 protein, mouse
• Superoxide Dismutase-1

Topics

• Amyotrophic Lateral Sclerosis (genetics, therapy)
• Animals
• CRISPR-Cas Systems
• Female
• Gene Deletion
• Gene Editing (methods)
• Genetic Therapy (methods)
• HEK293 Cells
• Humans
• Male
• Mice
• Muscle, Skeletal (metabolism, pathology)
• Mutation, Missense
• RNA, Guide, Kinetoplastida (genetics, metabolism)
• Superoxide Dismutase-1 (genetics, metabolism)