# miRNA-targeted auxin nuclear signalling elements orchestrate flower fate and drought response in yellow lupine

**Authors:** Milena Kulasek, Paulina Glazińska

PMC · DOI: 10.1038/s41598-025-22989-x · Scientific Reports · 2025-11-10

## TL;DR

This study explores how miRNAs and auxin signaling influence flower development and drought response in yellow lupine.

## Contribution

The study identifies miRNA-regulated auxin signaling elements that influence flower fate and drought response in yellow lupine.

## Key findings

- PCIB treatment increased retention of generative organs, highlighting auxin nuclear signaling's role in flower fate.
- miRNAs like MIR393, MIR160, and MIR167 regulate auxin pathway genes during flower development and drought stress.
- miRNA-target expression lacked a strictly negative correlation, suggesting other regulatory factors are involved.

## Abstract

Yellow lupine (Lupinus luteus L.) is a promising protein crop, but domestication has increased flower abscission. Flowers in higher whorls are more likely to abscise, providing a model to study factors influencing flower fate before abscission zone formation. We hypothesise that auxin localisation and miRNA-modulated signal transduction orchestrate flower development and abscission, particularly under drought. We investigated the indole-3-acetic acid (IAA) distribution in ovules and tested the effects of IAA, NPA (auxin transport inhibitor), and PCIB (auxin signalling blocker) on flower retention. Bioinformatic analyses of transcriptome data profiled miRNA-regulated auxin pathway elements (TIR1/AFBs, ARFs), with domain structures analysed for functional divergence. Selected miRNA-mRNA modules were analysed for their role in inflorescence drought response. IAA accumulation exhibited slight differences in upper pre-anthesis flowers. In the field experiment, PCIB treatment led to increased retention of generative organs, suggesting the vital role of auxin nuclear signalling in flower fate. Bioinformatic analyses identified miRNAs (MIR393, MIR160, MIR167, one novel) regulating TIR1/AFB and ARF6,8,17,18. qPCR revealed the differential expression of AFB3-, ARF6-, and ARF18-encoding transcripts and corresponding miR393, miR167, and miR160 during flower development and drought stress. However, miRNA-target expression lacked a strictly negative correlation, indicating other regulating players.

The online version contains supplementary material available at 10.1038/s41598-025-22989-x.

## Linked entities

- **Genes:** AFB3 (auxin signaling F-box 3) [NCBI Gene 837838], ARF6 (ARF GTPase 6) [NCBI Gene 382], ARF18 (auxin response factor 18) [NCBI Gene 825356]
- **Chemicals:** indole-3-acetic acid (PubChem CID 802), IAA (PubChem CID 802), NPA (PubChem CID 8594), PCIB (PubChem CID 2797)

## Full-text entities

- **Chemicals:** NPA (-), IAA (MESH:C030737), auxin (MESH:D007210)
- **Species:** Lupinus luteus (yellow lupine, species) [taxon 3873]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12603313/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12603313/full.md

## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12603313/full.md

---
Source: https://tomesphere.com/paper/PMC12603313