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Structural improvement of LidNA: delta-type LidNA is a potent miRNA inhibitor constructed with unmodified DNA

机译:LIDNA的结构改进:Delta型LIDNA是用未改性DNA构建的有效的miRNA抑制剂

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摘要

Many miRNA inhibitors have been developed, including chemically modified oligonucleotides, such as 2 '-O-methylated RNA and locked nucleic acid (LNA). Unmodified DNA has not yet been reported as a miRNA inhibitor due to relatively low DNA/miRNA binding affinity. We designed a structured DNA, LidNA, which was constructed with unmodified DNA, consisting of a complementary sequence to the target miRNA flanked by two structured DNA regions, such as double-stranded DNA. LidNA inhibited miRNA activity more potently than 2 '-O-methylated RNA or LNA. To optimize LidNA, two double-stranded regions were joined, causing the molecule to assume a delta-like shape, which we termed delta-type LidNA. Delta-type LidNAs were developed to target endogenous and exogenous miRNAs, and exhibited potent miRNA inhibitory effects with a duration of at least 10 days. Delta-type LidNA-21, which targeted miR-21, inhibited the growth of cancer cell lines. This newly developed LidNA could contribute to miRNA studies across multiple fields.
机译:已经开发了许多miRNA抑制剂,包括化学改性的寡核苷酸,例如2'-甲基化的RNA和锁定的核酸(LNA)。由于相对低的DNA / miRNA结合亲和力,未经修改的DNA尚未被报告为miRNA抑制剂。我们设计了由未经修改的DNA构建的结构化DNA,其构成,其由彼此侧翼的靶miRNA的互补序列组成,例如双链DNA。 LIDNA抑制比2'-甲基化的RNA或LNA更有效地抑制miRNA活性。为了优化LIDNA,连接了两个双链区域,使分子呈现δ状形状,其达到δ型LIDNA。 δ型LidNAS被开发成靶向内源性和外源性miRNA,并在至少10天的持续时间内表现出有效的miRNA抑制作用。靶向miR-21的Delta型Lidna-21抑制了癌细胞系的生长。这种新开发的LIDNA可以促进多个领域的miRNA研究。

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