category
bioRxiv
date
Feb 20, 2026
slug
status
Published
summary
发现哺乳动物Dicer中保守的带负电荷无序区域(IDR)通过与底物结合沟槽的电荷相互作用,稳定预切割状态以确保miRNA生成保真度,同时抑制RNAi活性;IDR的缺失会改变酶活性和底物特异性,揭示了无序蛋白区域在调控RNA酶功能中的关键作用。
tags
核酸蛋白工具酶
蛋白质进化
type
Post

📄 原文题目

A negatively charged unstructured loop autoinhibits mammalian Dicer and supports fidelity of miRNA biogenesis.

🔗 原文链接

💡 AI 核心解读

发现哺乳动物Dicer中保守的带负电荷无序区域(IDR)通过与底物结合沟槽的电荷相互作用,稳定预切割状态以确保miRNA生成保真度,同时抑制RNAi活性;IDR的缺失会改变酶活性和底物特异性,揭示了无序蛋白区域在调控RNA酶功能中的关键作用。

📝 英文原版摘要

Dicer RNases produce small RNAs for RNA interference (RNAi) and microRNA (miRNA) pathways. Although vertebrate Dicers share a conserved overall architecture with other eukaryotic Dicers, they are uniquely adapted for the production of gene-regulating miRNAs. We report here this adaptation extends beyond the structured core of the enzyme and relies on an intrinsically disordered region (IDR) conserved across jawed vertebrates. This negatively charged IDR supports fidelity of miRNA biogenesis while inhibiting RNAi. The IDR projects into a positively charged substrate-binding groove of Dicer and stabilizes a pre-dicing state, which effectively licenses authentic miRNA precursors. Electron cryo-microscopy shows that removal of the IDR shifts the equilibrium from the pre-dicing to the dicing state, thus increasing enzymatic activity and broadening substrate accessibility. In cells, deletion, replacement or variations of the IDR affect fidelity of microRNA biogenesis, change substrate specificity, and enhance RNAi. Altogether, our work highlights functional relevance of unstructured protein parts, which escape attention in structural analyses, and introduces an autoinhibitory IDR element mimicking negative RNA charge as a component of the molecular grammar governing IDRs in RNA-binding proteins.
造血祖细胞中HIV潜伏机制:GFI1作为关键调节因子剪接激活因子U2AF2在长非编码RNA PURPL和MALAT1内含子滞留中的非经典功能
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