Knauert M P, Glazer P M
Department of Therapeutic Radiology, Yale University School of Medicine, PO Box 208040, New Haven, CT 06520-8040, USA.
Hum Mol Genet. 2001 Oct 1;10(20):2243-51. doi: 10.1093/hmg/10.20.2243.
Sequence-specificity is the key to effective genetic targeting. With specificity, targeted genes can be manipulated in multiple ways; without it, gene therapy agents become loose canons within cells. Triplex forming oligonucleotides (TFOs) bind in the major groove of duplex DNA with high specificity and affinity. Because of these characteristics, TFOs have been proposed as homing devices for genetic manipulation in vivo. Here we review work demonstrating the ability of TFOs and related molecules to alter gene expression and mediate genome modification in mammalian cells. Recent studies have established that TFOs can mediate targeted gene knock out in mice, laying the foundation for the potential application of these molecules in human gene therapy.
序列特异性是有效基因靶向的关键。有了特异性,靶向基因就能以多种方式进行操控;没有特异性,基因治疗药物在细胞内就会变得不受控制。三链形成寡核苷酸(TFOs)以高特异性和亲和力结合于双链DNA的大沟中。由于这些特性,TFOs已被提议作为体内基因操控的归巢装置。在此,我们综述了证明TFOs及相关分子能够改变哺乳动物细胞基因表达并介导基因组修饰的研究工作。最近的研究证实,TFOs能够介导小鼠体内的靶向基因敲除,为这些分子在人类基因治疗中的潜在应用奠定了基础。