Induced cross-linking reactions to target genes using modified oligonucleotides

被引:18
|
作者
Nagatsugi, Fumi [1 ]
Imoto, Shuhei [2 ]
机构
[1] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Sendai, Miyagi 9808577, Japan
[2] Sojo Univ, Fac Pharmaceut Sci, Kumamoto 8600082, Japan
关键词
ANTISENSE OLIGONUCLEOTIDES; DNA; SITE; INHIBITION; SEQUENCE; 2-AMINO-6-VINYLPURINE; SELECTIVITY; ACTIVATION; SENSITIZES; EFFICIENT;
D O I
10.1039/c0ob00819b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Synthetic oligonucleotides (ONs) are valuable tools that interfere with gene expression by specifically binding to target genes in a sequence-specific manner. Reactive ONs containing cross-linking agents are expected to induce efficient inhibition because they bind covalently to target genes. In recent years, researchers have reported several cross-linking reactions that target DNA induced by external stimuli. This short review highlights recently developed novel cross-linking reactions, focusing particularly on nucleoside derivatives developed by our group.
引用
收藏
页码:2579 / 2585
页数:7
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