Solaiman F, Zink M A, Xu G, Grunkemeyer J, Cosgrove D, Saenz J, Hodgson C P
Creighton University School of Medicine, Omaha, Nebraska, USA.
Mol Reprod Dev. 2000 Jun;56(2 Suppl):309-15. doi: 10.1002/(SICI)1098-2795(200006)56:2+<309::AID-MRD22>3.0.CO;2-Y.
Retroviruses have been used for many years as vectors for human gene therapy as well as for making transgenic animals. However, the efficient insertion of genes by retroviruses is often complicated by transcriptional inactivation of the retroviral long terminal repeats (LTRs) and by the production of replication-competent retroviruses (RCR). Solutions to these and other difficulties are being found in modular vectors, in which the desirable features of different vector systems are combined. Examples of synergistic vectors include virosomes (liposome/virus delivery), adeno-retro vectors, and MLV/VL30 chimeras. As gene delivery systems become increasingly complex, methodology is also needed for precise assembly of modular vectors. Gene self-assembly (GENSA) technology permits seamless vector construction and simultaneous, multifragment assembly.
逆转录病毒多年来一直被用作人类基因治疗以及制造转基因动物的载体。然而,逆转录病毒高效插入基因的过程常常因逆转录病毒长末端重复序列(LTRs)的转录失活以及复制能力强的逆转录病毒(RCR)的产生而变得复杂。在模块化载体中正在找到这些及其他难题的解决方案,其中不同载体系统的理想特性被结合在一起。协同载体的例子包括病毒体(脂质体/病毒递送)、腺病毒-逆转录病毒载体和MLV/VL30嵌合体。随着基因递送系统变得越来越复杂,精确组装模块化载体也需要方法学。基因自组装(GENSA)技术允许无缝载体构建以及同时进行多片段组装。