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

Cell Rep. 2025 Sep 23;44(9):116162. doi: 10.1016/j.celrep.2025.116162. Epub 2025 Aug 19.

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.

MeSH terms

  • Animals
  • Argonaute Proteins / genetics
  • Argonaute Proteins / metabolism
  • Base Pairing
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / metabolism
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • RNA Stability* / genetics

Substances

  • MicroRNAs
  • Drosophila Proteins
  • Argonaute Proteins
  • AGO1 protein, Drosophila