封面:2-氨基-6-乙烯基-7-脱氮嘌呤脱氧核苷在 RNA 中的尿嘧啶选择性交联和对 miRNA 功能的抑制(ChemBioChem 21/2024)

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
ChemBioChem Pub Date : 2024-11-06 DOI:10.1002/cbic.202482101
Nadya Soemawisastra, Hidenori Okamura, Ahmed Mostafa Abdelhady, Kazumitsu Onizuka, Mamiko Ozawa, Fumi Nagatsugi
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引用次数: 0

摘要

微RNA(miRNA)通过RNA干扰调节基因表达。因此,miRNA 抑制剂,如抗 miRNA 寡核苷酸(AMOs),在治疗 miRNA 过度表达方面备受关注。在文章 10.1002/cbic.202400417 中,Fumi Nagatsugi 及其合作者证明了可交联核苷(2-氨基-7-脱氮-7-丙炔基-6-乙烯基嘌呤脱氧核苷;dADpVP)在双链杂交时与反尿嘧啶发生高反应性。此外,含有 dADpVP 的寡核苷酸靶向 mRNA 3′UTR 中的 miRNA 结合位点,通过共价形成有效抑制细胞中 miR21 的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Front Cover: Uracil-Selective Cross-Linking in RNA and Inhibition of miRNA Function by 2-Amino-6-vinyl-7-deazapurine Deoxynucleosides (ChemBioChem 21/2024)

Front Cover: Uracil-Selective Cross-Linking in RNA and Inhibition of miRNA Function by 2-Amino-6-vinyl-7-deazapurine Deoxynucleosides (ChemBioChem 21/2024)

MicroRNAs (miRNAs) regulate gene expression through RNA interference. Consequently, miRNA inhibitors, such as anti-miRNA oligonucleotides (AMOs), have attracted attention for treating miRNA overexpression. In article 10.1002/cbic.202400417, Fumi Nagatsugi and co-workers demonstrate that the cross-linkable nucleoside (2-amino-7-deaza-7-propynyl-6-vinylpurine deoxyriboside; dADpVP) reacted to counter uridine with high reactivity upon duplex hybridization. Moreover, the oligonucleotide containing dADpVP targeting the miRNA binding site in mRNA 3′UTR effectively inhibit the miR21 function in cells by covalent formation.

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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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