MdKIM1-MdMYB306 enhances apple resistance to Cytospora mali via brassinosteroid biosynthesis under sufficient potassium status

Clicks: 13
ID: 328074
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 #367 of 379 articles by views in The Plant cell

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 379 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
Potassium (K) supplementation enhances apple (Malus ×domestica) resistance to Cytospora mali, thereby reducing apple Cytospora canker occurrence in the field. Nevertheless, the molecular mechanisms underlying this K-enhanced resistance remain largely unelucidated. Here, we found that brassinosteroid (BR) biosynthesis was active in apple tissues under sufficient K (SK) conditions, resulting in an elevation of brassinolide (BL), the bioactive BR. Exogenous BL application under low K (LK) conditions restored apple resistance in both detached branches and field-grown trees, while the BR inhibitor brassinazole (BRZ) attenuated SK-dependent resistance. Notably, BR biosynthetic gene MdBR6ox2 was upregulated under SK conditions. Silencing of MdBR6ox2 reduced BL content and consequently compromised resistance to C. mali in SK apple calli. Furthermore, we identified that MdMYB306 is responsible for transactivating MdBR6ox2 expression via binding to the MBS cis-element in its promoter. Gene function analysis confirmed the positive role of MdMYB306 in regulating BR biosynthesis. Importantly, K supplementation facilitated the recruitment of MdKIM1, which interacts with MdMYB306 and induces conformational changes in MdMYB306, and enhances its transactivation capacity toward MdBR6ox2. Genetic evidence confirmed the importance of the MdKIM1-MdMYB306 module in initiating BR biosynthesis and increasing resistance in apple under SK status. Collectively, our findings uncovered a MdKIM1-MdMYB306-MdBR6ox2 module that promotes BR accumulation under SK conditions, providing a promising strategy for managing Cytospora canker via combined application K and BR.
Reference Key
openalex_W7212115968 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors
Journal The Plant cell
Year 2026
DOI
10.1093/plcell/koag261
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.