Pérez-Luz Sara, Díaz-Nido Javier
Departamento de Biología Molecular, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
J Biomed Biotechnol. 2010;2010. doi: 10.1155/2010/642804. Epub 2010 Aug 24.
Artificial chromosomes and minichromosome-like episomes are large DNA molecules capable of containing whole genomic loci, and be maintained as nonintegrating, replicating molecules in proliferating human somatic cells. Authentic human artificial chromosomes are very difficult to engineer because of the difficulties associated with centromere structure, so they are not widely used for gene-therapy applications. However, OriP/EBNA1-based episomes, which they lack true centromeres, can be maintained stably in dividing cells as they bind to mitotic chromosomes and segregate into daughter cells. These episomes are more easily engineered than true human artificial chromosomes and can carry entire genes along with all their regulatory sequences. Thus, these constructs may facilitate the long-term persistence and physiological regulation of the expression of therapeutic genes, which is crucial for some gene therapy applications. In particular, they are promising vectors for gene therapy in inherited diseases that are caused by recessive mutations, for example haemophilia A and Friedreich's ataxia. Interestingly, the episome carrying the frataxin gene (deficient in Friedreich's ataxia) has been demonstrated to rescue the susceptibility to oxidative stress which is typical of fibroblasts from Friedreich's ataxia patients. This provides evidence of their potential to treat genetic diseases linked to recessive mutations through gene therapy.
人工染色体和类微型染色体附加体是能够包含整个基因组位点的大型DNA分子,并能作为非整合、复制的分子在增殖的人类体细胞中维持。真正的人类人工染色体由于与着丝粒结构相关的困难而很难构建,因此它们没有广泛用于基因治疗应用。然而,基于OriP/EBNA1的附加体缺乏真正的着丝粒,它们可以在分裂细胞中稳定维持,因为它们能与有丝分裂染色体结合并分离到子细胞中。这些附加体比真正的人类人工染色体更容易构建,并且可以携带整个基因及其所有调控序列。因此,这些构建体可能有助于治疗性基因表达的长期维持和生理调节,这对一些基因治疗应用至关重要。特别是,它们是治疗由隐性突变引起的遗传性疾病(如甲型血友病和弗里德赖希共济失调)的有前景的载体。有趣的是,携带frataxin基因(弗里德赖希共济失调中缺失)的附加体已被证明能挽救弗里德赖希共济失调患者成纤维细胞典型的氧化应激易感性。这为它们通过基因治疗治疗与隐性突变相关的遗传疾病的潜力提供了证据。