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小干扰RNA种子区域的化学修饰通过空间位阻抑制与靶标的碱基配对来减少脱靶效应。

Chemical Modification of the siRNA Seed Region Suppresses Off-Target Effects by Steric Hindrance to Base-Pairing with Targets.

作者信息

Iribe Hanna, Miyamoto Kengo, Takahashi Tomoko, Kobayashi Yoshiaki, Leo Jastina, Aida Misako, Ui-Tei Kumiko

机构信息

Department of Computational Biology and Medical Science, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8581, Japan.

Center for Quantum Life Sciences and Department of Chemistry, Graduate School of Science, Hiroshima University, Higashi-Hiroshima 739-8526, Japan.

出版信息

ACS Omega. 2017 May 31;2(5):2055-2064. doi: 10.1021/acsomega.7b00291. Epub 2017 May 12.

Abstract

Chemical modifications of 2'-O-methyl (2'-OMe) and locked nucleic acid (LNA) of the nucleotides in the seed region (positions 2-8) of the small interfering RNA (siRNA) guide strand significantly reduced seed-matched (SM) off-target effects. The siRNA with 2'-OMe modifications inhibited the expression of a completely-matched (CM) target gene, whereas that with LNA modifications did not inhibit the expression of the CM target. By computational predictions of conformational changes of siRNA by these modifications, we revealed that both modifications in the siRNA seed region reduce SM off-target effects by steric hindrance to base-pairing with target transcripts but LNA modifications also disturb the association of the siRNA guide strand with the Argonaute (AGO) protein by altering RNA conformation. Thus, chemical modifications of the siRNA guide strand, which alter steric conformation to disturb base-pairing with target transcripts but do not disturb the association with the AGO protein, may successfully suppress off-target effects without substantial loss of RNA silencing activity.

摘要

对小干扰RNA(siRNA)引导链种子区域(第2至8位)核苷酸进行2'-O-甲基(2'-OMe)和锁核酸(LNA)化学修饰,可显著降低种子匹配(SM)脱靶效应。具有2'-OMe修饰的siRNA抑制完全匹配(CM)靶基因的表达,而具有LNA修饰的siRNA则不抑制CM靶基因的表达。通过对这些修饰的siRNA构象变化进行计算预测,我们发现siRNA种子区域的两种修饰均通过空间位阻减少与靶转录本的碱基配对来降低SM脱靶效应,但LNA修饰还通过改变RNA构象干扰siRNA引导链与AGO蛋白的结合。因此,对siRNA引导链进行化学修饰,改变空间构象以干扰与靶转录本的碱基配对,但不干扰与AGO蛋白的结合,可能成功抑制脱靶效应,而不会大幅丧失RNA沉默活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b09/6643817/7ea08e4e66c4/ao-2017-002912_0007.jpg

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