内源性靶向microRNA降解位点集群诱导不同microRNA家族的衰变。

Nicholas M Hiers, Lu Li, Tianqi Li, Peike Sheng, Yuzhi Wang, Conner M Traugot, Michael Yao, Mingyi Xie
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引用次数: 0

摘要

虽然对miRNA的生物发生和规范的miRNA靶向有很多了解,但对miRNA衰变的了解相对较少。在后生动物中,主要的miRNA衰变途径是通过靶定向miRNA降解(TDMD)介导的,其中某些rna可以“触发”miRNA衰变。所有已知的触发miRNA种子的TDMD碱基对,以及miRNA 3 '端广泛的碱基对,这种模式被认为诱导了Argonaute (Ago)的TDMD-competent构象变化,允许miRNA的转换。在这里,我们利用Ago1-CLASH发现果蝇转录本Kah包含至少两个触发器,一个“触发簇”,针对miR-9b和miR-279家族。其中一个触发器包含最小/非规范的3 '端碱基配对,但仍然足以诱导整个miR-279家族的TDMD。我们发现这些集群触发器可能缺乏协同性,最小的3'配对是miR-279家族周转所必需的,并探索了Kah触发簇的细胞内RNA结构。总的来说,这项研究扩展了内源性触发因素的列表和意想不到的复杂的miRNA降解调控网络。
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An endogenous cluster of target-directed microRNA degradation sites induces decay of distinct microRNA families.

While much is known about miRNA biogenesis and canonical miRNA targeting, relatively less is understood about miRNA decay. The major miRNA decay pathway in metazoans is mediated through target-directed miRNA degradation (TDMD), in which certain RNAs can "trigger" miRNA decay. All known triggers for TDMD base pair with the miRNA seed, and extensively base pair on the miRNA 3' end, a pattern that supposedly induces a TDMD-competent conformational change of Argonaute (Ago), allowing for miRNA turnover. Here, we utilized Ago1-CLASH to find that the Drosophila transcript Kah contains at least two triggers, a "trigger cluster", against miR-9b and the miR-279 family. One of these triggers contains minimal/non-canonical 3' end base pairing but is still sufficient to induce TDMD of the entire miR-279 family. We found that these clustered triggers likely lack cooperativity, the minimal 3' pairing is required for miR-279 family turnover, and probed the in-cell RNA structure of the Kah trigger cluster. Overall, this study expands the list of endogenous triggers and the unexpectedly complex regulatory network governing miRNA degradation.

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