【摘 要】
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We here report a genome-editing strategy to correct spinal muscular atrophy (SMA).Rather than directly targeting the pathogenic exonic mutations,our strategy em
【机 构】
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Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical
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We here report a genome-editing strategy to correct spinal muscular atrophy (SMA).Rather than directly targeting the pathogenic exonic mutations,our strategy employed Cas9 and guide-sgRNA for the targeted disruption ofintronic splicing-regulatory elements.We disrupted intronic splicing silencers (ISSs,including ISS-N1 and ISS + 100) of survival motor neuron (SMN) 2,a key modifier gene of SMA,to enhance exon 7 inclusion and full-length SMN expression in SMA iPSCs.Survival of splicing-corrected iPSC-derived motor neurons was rescued with SMN restoration.Furthermore,co-injection of Cas9 mRNA from Streptococcus pyogenes (SpCas9) or Cas9 from Staphylococcus aureus (SaCas9) alongside their corresponding sgRNAs targeting ISS-N1 into zygotes rescued 56% and 100% of severe SMA transgenic mice (Smn-/-,SM-N2tg/-).The median survival of the resulting mice was extended to >400 days.Collectively,our study provides proof-of-principle for a new strategy to therapeutically intervene in SMA and other RNA-splicing-related diseases.
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