An endogenous cluster of target-directed microRNA degradation sites induces decay of distinct microRNA families

内源性靶向microRNA降解位点簇诱导不同microRNA家族的衰变

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作者:Nicholas M Hiers ,Lu Li ,Tianqi Li ,Peike Sheng ,Yuzhi Wang ,Conner M Traugot ,Michael Yao ,Mingyi Xie

Abstract

While much is known about microRNA (miRNA) biogenesis and targeting, relatively less is understood about miRNA decay. Target-directed miRNA degradation (TDMD) is a mechanism in metazoans where certain RNAs can "trigger" miRNA decay. All known TDMD triggers base pair with the miRNA seed, and extensively base pair on the miRNA 3' end, a pattern that is believed to be a requirement for miRNA turnover. Using Ago1-CLASH, we find that the Drosophila transcript Kah contains at least two triggers, a "trigger cluster," against miR-9b and the miR-279 family. One trigger contains minimal/non-canonical 3' end base-pairing but is still sufficient to induce TDMD of the miR-279 family. We find that these clustered triggers lack cooperativity, that minimal 3' pairing is required for miR-279 family turnover, and probed the in-cell structure of the Kah trigger cluster. Overall, we expand the list of endogenous TDMD triggers, which revealed unexpectedly complex regulation in miRNA turnover. Keywords: AGO-CLASH; CP: Molecular biology; SHAPE; TDMD; microRNA.

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