Würtele H, Little K C E, Chartrand P
Programme de Biologie Moléculaire, Université de Montréal, Montréal, Canada.
Gene Ther. 2003 Oct;10(21):1791-9. doi: 10.1038/sj.gt.3302074.
Foreign DNA integration is one of the most widely exploited cellular processes in molecular biology. Its technical use permits us to alter a cellular genome by incorporating a fragment of foreign DNA into the chromosomal DNA. This process employs the cell's own endogenous DNA modification and repair machinery. Two main classes of integration mechanisms exist: those that draw on sequence similarity between the foreign and genomic sequences to carry out homology-directed modifications, and the nonhomologous or 'illegitimate' insertion of foreign DNA into the genome. Gene therapy procedures can result in illegitimate integration of introduced sequences and thus pose a risk of unforeseeable genomic alterations. The choice of insertion site, the degree to which the foreign DNA and endogenous locus are modified before or during integration, and the resulting impact on structure, expression, and stability of the genome are all factors of illegitimate DNA integration that must be considered, in particular when designing genetic therapies.
外源DNA整合是分子生物学中应用最为广泛的细胞过程之一。其技术应用使我们能够通过将一段外源DNA片段整合到染色体DNA中,从而改变细胞基因组。这一过程利用了细胞自身的内源性DNA修饰和修复机制。存在两类主要的整合机制:一类是利用外源序列与基因组序列之间的序列相似性来进行同源定向修饰;另一类是外源DNA非同源或“非法”插入基因组。基因治疗程序可能导致导入序列的非法整合,从而带来不可预见的基因组改变风险。插入位点的选择、外源DNA与内源性基因座在整合前或整合过程中被修饰的程度,以及对基因组结构、表达和稳定性产生的影响,都是非法DNA整合时必须考虑的因素,尤其是在设计基因治疗时。