PlMYB51 and PlMYB1R1 switch PlABI5 - PlCesA6 function to regulate seed dormancy and germination in Paeonia lactiflora

Clicks: 7
ID: 337814
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #642 of 650 articles by views in Plant physiology and biochemistry : PPB

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 650 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Seed dormancy is a key strategy for plants to adapt to fluctuating environments and ensure population propagation. Paeonia lactiflora seeds exhibit typical double dormancy, characterized by a prolonged germination cycle and low emergence rate that severely restrict their large-scale propagation. Although ABI5, the core transcription factor (TF) in the abscisic acid (ABA) signaling pathway, acts as a critical hub in maintaining seed dormancy, its upstream dynamic regulatory mechanism and downstream cell-wall-related target genes remain largely unknown. In this study, two upstream regulators of PlABI5, PlMYB51 and PlMYB1R1, were identified via yeast one-hybrid screening, and their regulatory mechanism was characterized. The results showed that both PlMYB51 and PlMYB1R1 belonged to the R2R3-MYB family. When acting alone, they directly bound to and activated the PlABI5 promoter, inhibiting seed germination. Upon forming a protein complex in the nucleus, their regulatory function was reversed and they repressed PlABI5 transcription to promote germination, supporting a proposed monomer activation-complex inhibition switch model. Furthermore, PlABI5 specifically targeted the PlCesA6 promoter and inhibited its expression without affecting the homolog PlCesA3. PlCesA6 positively regulated seed germination by promoting hypocotyl cell elongation, and its overexpression rescued the inhibition caused by PlMYB51/PlMYB1R1 overexpression. Collectively, this study proposes a working model for the PlMYB51/PlMYB1R1-PlABI5-PlCesA6 cascade in controlling seed dormancy and germination, and identifies a putative functional switching mode of MYB TFs mediated by protein-protein interactions. These findings provide key gene resources and a theoretical basis for artificial dormancy breaking and molecular breeding in P. lactiflora.
Reference Key
openalex_W7224633579 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors
Journal Plant physiology and biochemistry : PPB
Year 2026
DOI
10.1093/plphys/kiag804
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.