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Single amino acid change alters specificity of the multi-allelic wheat stem rust resistance locus SR9

Author

Listed:
  • Jianping Zhang

    (CSIRO Agriculture & Food
    University of Sydney
    Henan Agricultural University)

  • Jayaveeramuthu Nirmala

    (University of Minnesota)

  • Shisheng Chen

    (Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agricultural Sciences at Weifang)

  • Matthias Jost

    (CSIRO Agriculture & Food)

  • Burkhard Steuernagel

    (John Innes Centre, Norwich Research Park)

  • Mirka Karafiatova

    (Centre of the Region Haná for Biotechnological and Agricultural Research)

  • Tim Hewitt

    (CSIRO Agriculture & Food)

  • Hongna Li

    (Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agricultural Sciences at Weifang)

  • Erena Edae

    (University of Minnesota)

  • Keshav Sharma

    (Cereal Disease Laboratory)

  • Sami Hoxha

    (University of Sydney)

  • Dhara Bhatt

    (CSIRO Agriculture & Food)

  • Rea Antoniou-Kourounioti

    (University of Glasgow)

  • Peter Dodds

    (CSIRO Agriculture & Food)

  • Brande B. H. Wulff

    (King Abdullah University of Science and Technology (KAUST)
    Centre for Desert Agriculture, KAUST)

  • Jaroslav Dolezel

    (Centre of the Region Haná for Biotechnological and Agricultural Research)

  • Michael Ayliffe

    (CSIRO Agriculture & Food)

  • Colin Hiebert

    (Agriculture and Agri-Food Canada, Morden Research and Development Centre)

  • Robert McIntosh

    (University of Sydney)

  • Jorge Dubcovsky

    (University of California
    Howard Hughes Medical Institute)

  • Peng Zhang

    (University of Sydney)

  • Matthew N. Rouse

    (University of Minnesota
    Cereal Disease Laboratory)

  • Evans Lagudah

    (CSIRO Agriculture & Food
    University of Sydney)

Abstract

Most rust resistance genes thus far isolated from wheat have a very limited number of functional alleles. Here, we report the isolation of most of the alleles at wheat stem rust resistance gene locus SR9. The seven previously reported resistance alleles (Sr9a, Sr9b, Sr9d, Sr9e, Sr9f, Sr9g, and Sr9h) are characterised using a synergistic strategy. Loss-of-function mutants and/or transgenic complementation are used to confirm Sr9b, two haplotypes of Sr9e (Sr9e_h1 and Sr9e_h2), Sr9g, and Sr9h. Each allele encodes a highly related nucleotide-binding site leucine-rich repeat (NB-LRR) type immune receptor, containing an unusual long LRR domain, that confers resistance to a unique spectrum of isolates of the wheat stem rust pathogen. The only SR9 protein effective against stem rust pathogen race TTKSK (Ug99), SR9H, differs from SR9B by a single amino acid. SR9B and SR9G resistance proteins are also distinguished by only a single amino acid. The SR9 allelic series found in the B subgenome are orthologs of wheat stem rust resistance gene Sr21 located in the A subgenome with around 85% identity in protein sequences. Together, our results show that functional diversification of allelic variants at the SR9 locus involves single and multiple amino acid changes that recognize isolates of wheat stem rust.

Suggested Citation

  • Jianping Zhang & Jayaveeramuthu Nirmala & Shisheng Chen & Matthias Jost & Burkhard Steuernagel & Mirka Karafiatova & Tim Hewitt & Hongna Li & Erena Edae & Keshav Sharma & Sami Hoxha & Dhara Bhatt & Re, 2023. "Single amino acid change alters specificity of the multi-allelic wheat stem rust resistance locus SR9," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42747-9
    DOI: 10.1038/s41467-023-42747-9
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    References listed on IDEAS

    as
    1. Sean Walkowiak & Liangliang Gao & Cecile Monat & Georg Haberer & Mulualem T. Kassa & Jemima Brinton & Ricardo H. Ramirez-Gonzalez & Markus C. Kolodziej & Emily Delorean & Dinushika Thambugala & Valent, 2020. "Multiple wheat genomes reveal global variation in modern breeding," Nature, Nature, vol. 588(7837), pages 277-283, December.
    2. Kathryn Tunyasuvunakool & Jonas Adler & Zachary Wu & Tim Green & Michal Zielinski & Augustin Žídek & Alex Bridgland & Andrew Cowie & Clemens Meyer & Agata Laydon & Sameer Velankar & Gerard J. Kleywegt, 2021. "Highly accurate protein structure prediction for the human proteome," Nature, Nature, vol. 596(7873), pages 590-596, August.
    3. John Jumper & Richard Evans & Alexander Pritzel & Tim Green & Michael Figurnov & Olaf Ronneberger & Kathryn Tunyasuvunakool & Russ Bates & Augustin Žídek & Anna Potapenko & Alex Bridgland & Clemens Me, 2021. "Highly accurate protein structure prediction with AlphaFold," Nature, Nature, vol. 596(7873), pages 583-589, August.
    4. Jianping Zhang & Timothy C. Hewitt & Willem H. P. Boshoff & Ian Dundas & Narayana Upadhyaya & Jianbo Li & Mehran Patpour & Sutha Chandramohan & Zacharias A. Pretorius & Mogens Hovmøller & Wendelin Sch, 2021. "A recombined Sr26 and Sr61 disease resistance gene stack in wheat encodes unrelated NLR genes," Nature Communications, Nature, vol. 12(1), pages 1-8, December.
    5. Guotai Yu & Oadi Matny & Nicolas Champouret & Burkhard Steuernagel & Matthew J. Moscou & Inmaculada Hernández-Pinzón & Phon Green & Sadiye Hayta & Mark Smedley & Wendy Harwood & Ngonidzashe Kangara & , 2022. "Aegilops sharonensis genome-assisted identification of stem rust resistance gene Sr62," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
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