Storici Francesca
Georgia Institute of Technology, School of Biology, 310 Ferst Drive, Atlanta, GA 30332, USA.
Curr Opin Mol Ther. 2008 Jun;10(3):224-30.
Oligonucleotides represent the most versatile and high-throughput tool for introducing specific modifications in the genome of living cells. These short nucleic acid molecules can be designed and synthesized in large amounts, dispensing with laborious cloning, in vitro mutagenesis and extensive sequencing procedures. Oligonucleotides, which are utilized for in vivo mutagenesis in organisms ranging from bacteria to mammalian cells, are composed of DNA residues only, or DNA with a complementary RNA tract (chimeras) folded into a double hairpin structure. It is generally believed that the DNA stretch functions to correct the genomic alteration, while the RNA part, when present, serves to stabilize the duplex. RNA bases, as well as RNA molecules, can also have a direct and active role in genome modification and remodeling. The development of strategies that can exploit such unique RNA functions may have important implications in gene targeting and gene therapy, especially considering that RNA molecules mimicking RNA oligonucleotides could be generated directly in the nucleus of targeted cells via transcription from viral vectors.
寡核苷酸是在活细胞基因组中引入特定修饰的最通用且高通量的工具。这些短核酸分子可以大量设计和合成,无需繁琐的克隆、体外诱变和广泛的测序程序。用于从细菌到哺乳动物细胞等生物体体内诱变的寡核苷酸仅由DNA残基组成,或者由带有折叠成双发夹结构的互补RNA片段(嵌合体)的DNA组成。一般认为,DNA片段起到纠正基因组改变的作用,而RNA部分(如果存在)则用于稳定双链体。RNA碱基以及RNA分子在基因组修饰和重塑中也可以发挥直接且积极的作用。开发能够利用此类独特RNA功能的策略可能在基因靶向和基因治疗中具有重要意义,特别是考虑到可以通过病毒载体在靶向细胞核中直接转录产生模拟RNA寡核苷酸的RNA分子。