Site-specific DNA photocleavage and photomodulation by oligonucleotide conjugates.

Oligonucleotides Pub Date : 2010-12-01 Epub Date: 2010-09-23 DOI:10.1089/oli.2010.0247
Netanel Kolevzon, Eylon Yavin
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引用次数: 6

Abstract

Triplex-forming oligonucleotides have been explored in the last 3 decades as highly specific gene-modifying agents. Such agents have been showed to either upregulate or shut down gene expression in vitro, an outcome that depends on the specifically designed biological system. One interesting approach is to tether to the oligonucleotide a photoreactive moiety. After hybridization to the DNA target (typically single- or double-stranded DNA), a site-specific photoinduced reaction may take place at a timely manner. Further, as the light source may be focused at a certain area, one has control on the location at which the phototriggered DNA modification takes place. In this regard, the use of tissue-penetrating photons (typically 630-950 nm) would be most relevant for in vivo applications as photoactivation may lead to site-specific DNA modification at a specific tissue/organ. In this review we highlight the advances made in this field and discuss the hurdles that lay ahead for the realization of phototriggered triplex-forming oligonucleotides as a solid therapeutic approach.

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寡核苷酸偶联物的位点特异性DNA光切割和光调节。
在过去的30年里,三聚体形成的寡核苷酸被作为高度特异性的基因修饰剂进行了探索。这些药物已被证明可以上调或关闭体外基因表达,其结果取决于特定设计的生物系统。一种有趣的方法是将一个光反应片段拴在寡核苷酸上。与靶DNA(通常为单链或双链DNA)杂交后,可及时发生位点特异性光诱导反应。此外,由于光源可以聚焦在某个区域,人们可以控制光触发DNA修饰发生的位置。在这方面,组织穿透光子(通常为630-950 nm)的使用将与体内应用最为相关,因为光激活可能导致特定组织/器官的位点特异性DNA修饰。在这篇综述中,我们强调了在这一领域取得的进展,并讨论了实现光触发三聚体形成寡核苷酸作为一种固体治疗方法的障碍。
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Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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