Gammage Payam A, Rorbach Joanna, Vincent Anna I, Rebar Edward J, Minczuk Michal
Medical Research Council, Mitochondrial Biology Unit, Cambridge, UK.
EMBO Mol Med. 2014 Apr;6(4):458-66. doi: 10.1002/emmm.201303672. Epub 2014 Feb 24.
We designed and engineered mitochondrially targeted obligate heterodimeric zinc finger nucleases (mtZFNs) for site-specific elimination of pathogenic human mitochondrial DNA (mtDNA). We used mtZFNs to target and cleave mtDNA harbouring the m.8993T>G point mutation associated with neuropathy, ataxia, retinitis pigmentosa (NARP) and the "common deletion" (CD), a 4977-bp repeat-flanked deletion associated with adult-onset chronic progressive external ophthalmoplegia and, less frequently, Kearns-Sayre and Pearson's marrow pancreas syndromes. Expression of mtZFNs led to a reduction in mutant mtDNA haplotype load, and subsequent repopulation of wild-type mtDNA restored mitochondrial respiratory function in a CD cybrid cell model. This study constitutes proof-of-principle that, through heteroplasmy manipulation, delivery of site-specific nuclease activity to mitochondria can alleviate a severe biochemical phenotype in primary mitochondrial disease arising from deleted mtDNA species.
我们设计并构建了线粒体靶向的专一性异源二聚体锌指核酸酶(mtZFNs),用于对致病性人类线粒体DNA(mtDNA)进行位点特异性清除。我们使用mtZFNs靶向并切割携带与神经病变、共济失调、色素性视网膜炎(NARP)相关的m.8993T>G点突变以及“常见缺失”(CD)的mtDNA,“常见缺失”是一种4977 bp的重复序列侧翼缺失,与成人发病的慢性进行性眼外肌麻痹相关,较少与卡恩斯-塞尔综合征和皮尔逊骨髓胰腺综合征相关。mtZFNs的表达导致突变型mtDNA单倍型负荷降低,随后野生型mtDNA的重新增殖恢复了CD细胞杂交模型中的线粒体呼吸功能。这项研究构成了原理验证,即通过异质性操作,将位点特异性核酸酶活性传递到线粒体可以缓解由缺失的mtDNA物种引起的原发性线粒体疾病中的严重生化表型。