Department of Life Science, Tokyo Institute of Technology, 4259 Nagatsuta, Midoriku, Yokohama 226-8501, Japan.
Org Lett. 2013 Sep 6;15(17):4386-9. doi: 10.1021/ol401917r. Epub 2013 Aug 16.
U1 snRNA is an interesting biological tool for splicing correction and regulation of gene expression. However, U1 snRNA has never been chemically synthesized. In this study, the first chemical synthesis of U1snRNA and its analogues was carried out. Moreover, it was found that the binding affinity of the modified U1 snRNA with an ethylene glycol linkage to snurportin 1 (nuclear import adaptor) was as high as that of the unmodified RNA.
U1 snRNA 是一种用于剪接校正和基因表达调控的有趣的生物工具。然而,U1 snRNA 从未被化学合成过。在本研究中,首次进行了 U1snRNA 及其类似物的化学合成。此外,还发现具有乙二醇键的修饰 U1 snRNA 与 snurportin 1(核导入接头)的结合亲和力与未修饰的 RNA 一样高。