Abstract
Cloning of resistance genes expands our understanding of their function and facilitates their deployment in breeding. Here we report the cloning of two genes from wild emmer wheat (Triticum turgidum ssp. dicoccoides) underlying Yr84-mediated stripe rust resistance using a combination of fine mapping, long-read sequencing and mutation-induced functional validation. In contrast to all previously cloned stripe rust genes, the incompletely dominant Yr84 phenotype is conferred through the coordinated function of paired nucleotide-binding leucine-rich repeat (NLR) genes CNL and NL. We reason that based on their genomic organization, annotation, expression profiles and predicted protein structure, CNL functions as a sensor NLR, responsible for effector recognition, and NL acts as a helper NLR, initiating downstream resistance cascades. Both the CNL and NL lack an integrated domain(s) previously implicated in effector recognition by paired NLRs; therefore, these findings contribute insights into the structure and molecular mechanisms of the function of plant paired NLRs.
| Original language | English |
|---|---|
| Pages (from-to) | 1535-1542 |
| Number of pages | 8 |
| Journal | Nature Genetics |
| Volume | 57 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 2025 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© The Author(s), under exclusive licence to Springer Nature America, Inc. 2025.
ASJC Scopus subject areas
- Genetics
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