用于治疗性RNA切割和去靶向的哺乳动物microrna的绝对定量。

IF 4.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
RNA Pub Date : 2025-05-28 DOI:10.1261/rna.080566.125
Carolyn Kraus, Jiayi Wang, Haiying Zheng, Jennifer Broderick, Nandagopal Ajaykumar, Mina Zamani, Mengqi Yang, Katharine Cecchini, Shun-Qing Liang, Olena Kolumba, Kathryn Chase, Jooyoung Lee, Wen Xue, Erik Sontheimer, Ildar Gainetdinov
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引用次数: 0

摘要

MicroRNAs (miRNAs)是一种小的调控rna,它可以破坏部分互补的转录物的稳定性,并切割完美配对的靶标。mirna通常在特定的组织中表达,允许mirna定向切割用于防止无意的细胞类型的基因组编辑或基因替代疗法,这种策略称为去靶向。细胞内miRNA浓度影响基因沉默的效力,但在哺乳动物组织中仅确定了少数miRNA的绝对稳态水平。在这里,我们报告了14种人和小鼠细胞系以及17种小鼠组织(包括8个大脑区域)中mirna的绝对丰度。我们在人类培养细胞中的实验表明,miRNA和靶水平都会影响完全互补转录本的切割效果。我们报告了高表达转录物高效切割所需的miRNA浓度,并鉴定了在体内达到该阈值的小鼠miRNA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Absolute Quantification of Mammalian MicroRNAs for Therapeutic RNA Cleavage and Detargeting.

MicroRNAs (miRNAs) are small regulatory RNAs that destabilize partially complementary transcripts and cleave perfectly paired targets. miRNAs are often expressed in a specific tissue, allowing miRNA-directed cleavage to be used to prevent genome editing or gene replacement therapy in unintended cell types, a strategy called detargeting. miRNA intracellular concentration influences the potency of gene silencing, yet the absolute steady-state levels of just a few miRNAs have been determined in mammalian tissues. Here, we report the absolute abundance of miRNAs in 14 human and mouse cell lines and 17 mouse tissues, including eight brain regions. Our experiments in human cultured cells demonstrate that both miRNA and target levels influence efficacy of cleavage of fully complementary transcripts. We report the miRNA concentration required for productive cleavage of highly expressed transcripts and identify mouse miRNAs that reach this threshold in vivo.

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来源期刊
RNA
RNA 生物-生化与分子生物学
CiteScore
8.30
自引率
2.20%
发文量
101
审稿时长
2.6 months
期刊介绍: RNA is a monthly journal which provides rapid publication of significant original research in all areas of RNA structure and function in eukaryotic, prokaryotic, and viral systems. It covers a broad range of subjects in RNA research, including: structural analysis by biochemical or biophysical means; mRNA structure, function and biogenesis; alternative processing: cis-acting elements and trans-acting factors; ribosome structure and function; translational control; RNA catalysis; tRNA structure, function, biogenesis and identity; RNA editing; rRNA structure, function and biogenesis; RNA transport and localization; regulatory RNAs; large and small RNP structure, function and biogenesis; viral RNA metabolism; RNA stability and turnover; in vitro evolution; and RNA chemistry.
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