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June 5, 2026Genetics0 citations

A single non-coding RNA locus produces small and long regulatory RNAs with distinct biological functions

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TCTravis D. CarneyHSHalyna R. Shcherbata

Key Points

  • This research aims to explore the role of non-coding RNAs, specifically miR-317 and Peony, in stem cell biology and tumorigenesis in Drosophila.
  • Utilized Drosophila melanogaster testes to study non-coding RNA effects.
  • Identified miR-317 and Peony as products of a polycistronic locus with differential expression due to alternative polyadenylation.
  • Assessed the biological impact of miR-317 deficiency on Notch signaling and germ-cell tumors.
  • Absence of miR-317 leads to germ-cell tumors in developing Drosophila.
  • Increased Peony expression disrupts muscle sheath structure around testes.
  • miR-317 deficiency increases Notch signaling activity and upregulates its predicted targets.

Abstract

Abstract The impact of non-coding RNAs on stem cell biology and differentiation processes is an important and incompletely understood area of research. Using the testes of Drosophila melanogaster as a proven model for investigating these processes, we identified a polycistronic locus from which two non-coding transcripts, miR-317 and the long non-coding RNA Peony, are produced, with alternative polyadenylation implicated in regulation of their differential expression levels. We report here that each transcript has a distinct role in Drosophila testes; the absence of miR-317 leads to the emergence of germ-cell tumors in developing flies, and the increased expression of Peony results in the disruption of the muscle sheath covering the testis. We also show that miR-317 deficiency increases Notch signaling activity in somatic cyst cells, upregulates multiple predicted targets of miR-317, and drives germline tumorigenesis. Our findings establish miR-317 as a tumor suppressor controlling Notch signaling strength and uncover alternative polyadenylation as an unrecognized mechanism governing miRNA expression.

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Cite This Study

Carney et al. (2026) studied this question.

synapsesocial.com/papers/6a22698b763171746d5481dehttps://doi.org/10.1093/genetics/iyag141
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