# Noncoding RNAs and the phytochemical economy: Molecular regulators of secondary metabolism in medicinal plants

**Authors:** Okechukwu Paul-Chima Ugwu, Melvin Nnaaemeka Ugwu, Hope Onohuean, Hilal Ahmad Rather, Ibe Michael Usman

PMC · DOI: 10.1016/j.bbrep.2026.102486 · 2026-02-09

## TL;DR

This paper explores how noncoding RNAs regulate the production of medicinal plant compounds, highlighting their role in controlling specialized metabolites.

## Contribution

The paper systematically reviews how different types of noncoding RNAs regulate secondary metabolism in medicinal plants, identifying gaps and translational opportunities.

## Key findings

- Noncoding RNAs like miRNAs and siRNAs regulate key enzymes and transcription factors in secondary metabolic pathways.
- lncRNAs and circRNAs influence metabolite profiles through chromatin remodeling and ceRNA networks.
- Validation of ncRNA roles in medicinal plants is limited, with a need for better databases and multi-omics approaches.

## Abstract

Medicinal plants produce specialised (secondary) metabolites including alkaloids, terpenoids, flavonoids and phenolics that underpin pharmaceuticals, nutraceuticals and traditional therapeutics. Although enzyme-encoding genes and transcription factors are established regulators of these pathways, accumulating evidence indicates that noncoding RNAs (ncRNAs) provide additional, and in some contexts decisive, regulatory control.

To synthesise and critically appraise evidence on how plant ncRNAs microRNAs (miRNAs), small interfering RNAs (siRNAs), long noncoding RNAs (lncRNAs) and circular RNAs (circRNAs) regulate secondary metabolism in medicinal plants, and to map translational opportunities and unresolved gaps.

We conducted a narrative review with a systematic synthesis across PubMed/MEDLINE, Scopus, Web of Science Core Collection, CAB Abstracts and AGRICOLA, supplemented by Google Scholar screening using SANRA.

Across medicinal and non-model plant systems, miRNAs repeatedly target transcription factors that control biosynthetic pathways (e.g., MYB/bHLH/WRKY families) and, in some cases, key enzymes (e.g., PAL/CHS/DFR modules), thereby supporting stress-responsive and developmentally timed reprogramming of metabolite profiles. siRNAs contribute through RNA-directed DNA methylation (RdDM) and regulation of transposons and gene clusters. lncRNAs modulate chromatin accessibility and function as scaffolds or decoys, including as competing endogenous RNA (ceRNA) ‘sponges’, whereas circRNAs are emerging as relatively stable regulatory hubs that may influence miRNA availability and stress-associated transcriptional states. Evidence quality varies across ncRNA classes and species, and mechanistic validation in medicinal plants remains inconsistent.

ncRNAs constitute a multilayer regulatory system shaping the ‘phytochemical economy’ of medicinal plants. Progress towards translation will require standardised ncRNA annotation resources, rigorous causal validation, and integrated multi-omics study designs to support precision metabolic engineering and sustainable phytochemical production.

Image 1

•NcRNAs (miRNAs, siRNAs, lncRNAs, circRNAs) regulate specialised metabolism.•Evidence supports ncRNA control of MYB/bHLH/WRKY TFs and key enzymes in pathways.•LncRNA/circRNA ceRNA networks and chromatin remodelling shape tissue metabolites.•Gaps: limited validation in medicinal species, ncRNA databases, and causal omics.

NcRNAs (miRNAs, siRNAs, lncRNAs, circRNAs) regulate specialised metabolism.

Evidence supports ncRNA control of MYB/bHLH/WRKY TFs and key enzymes in pathways.

LncRNA/circRNA ceRNA networks and chromatin remodelling shape tissue metabolites.

Gaps: limited validation in medicinal species, ncRNA databases, and causal omics.

## Linked entities

- **Genes:** MYB (MYB proto-oncogene, transcription factor) [NCBI Gene 4602], Bhlha15 (basic helix-loop-helix family, member a15) [NCBI Gene 25334], WRKY (probable WRKY transcription factor 33) [NCBI Gene 103865671], PAM (peptidylglycine alpha-amidating monooxygenase) [NCBI Gene 5066], LYST (lysosomal trafficking regulator) [NCBI Gene 1130], DFR (dihydroflavonol 4-reductase) [NCBI Gene 544150]

## Full-text entities

- **Genes:** MYB (MYB proto-oncogene, transcription factor) [NCBI Gene 4602] {aka Cmyb, c-myb, c-myb_CDS, efg}, LYST (lysosomal trafficking regulator) [NCBI Gene 1130] {aka CHS, CHS1, Mauve}, LRIT1 (leucine rich repeat, Ig-like and transmembrane domains 1) [NCBI Gene 26103] {aka FIGLER9, LRRC21, PAL}
- **Chemicals:** phenolics (-), flavonoids (MESH:D005419), alkaloids (MESH:D000470), terpenoids (MESH:D013729)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12907886/full.md

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Source: https://tomesphere.com/paper/PMC12907886