Stella Cesari, John Moore, Chunhong Chen, Daryl Webb, Sambasivam Periyannan, Rohit Mago, Maud Bernoux, Evans S. Lagudah, and Peter N. Dodd

Significance

Stem rust caused by the fungus Puccinia graminis f. sp. tritici (Pgt) remains the major disease threat to wheat production. The Sr33 and Sr50 resistance proteins protect wheat against a broad spectrum of field isolates of Pgt and are closely related to the barley powdery mildew-resistance protein MLA10. Like MLA10, Sr33 and Sr50 possess signaling N-terminal domains that self-associate in planta and initiate cell-death signaling from the cytosol. However, Sr33 induces disease-resistance signaling from the cytosol but not from the nucleus of wheat cells, suggesting cytosolic activation of both cell death and stem rust resistance. 

Abstract

Plants possess intracellular immune receptors designated “nucleotide-binding domain and leucine-rich repeat” (NLR) proteins that translate pathogen-specific recognition into disease-resistance signaling. The wheat immune receptors Sr33 and Sr50 belong to the class of coiled-coil (CC) NLRs. They confer resistance against a broad spectrum of field isolates of Puccinia graminis f. sp. tritici, including the Ug99 lineage, and are homologs of the barley powdery mildew-resistance protein MLA10. Here, we show that, similarly to MLA10, the Sr33 and Sr50 CC domains are sufficient to induce cell death in Nicotiana benthamiana. Autoactive CC domains and full-length Sr33 and Sr50 proteins self-associate in planta. In contrast, truncated CC domains equivalent in size to an MLA10 fragment for which a crystal structure was previously determined fail to induce cell death and do not self-associate. Mutations in the truncated region also abolish self-association and cell-death signaling. Analysis of Sr33 and Sr50 CC domains fused to YFP and either nuclear localization or nuclear export signals in N. benthamiana showed that cell-death induction occurs in the cytosol. In stable transgenic wheat plants, full-length Sr33 proteins targeted to the cytosol provided rust resistance, whereas nuclear-targeted Sr33 was not functional. These data are consistent with CC-mediated induction of both cell-death signaling and stem rust resistance in the cytosolic compartment, whereas previous research had suggested that MLA10-mediated cell-death and disease resistance signaling occur independently, in the cytosol and nucleus, respectively.

See: http://www.pnas.org/content/113/36/10204.full

PNAS September 6, 2016 vol. 113 no. 36: 10204–10209

Fig. 1. The full CC domains of MLA10, Sr33, and Sr50 are sufficient for autoactivity in planta. Indicated fragments of the MLA10, Sr33, and Sr50 proteins fused to HA or CFP were transiently expressed in N. benthamiana leaves by Agrobacterium tumefaciens infiltration along with the autoactive RGA4:HA or RGA4:CFP positive controls and the inactive rga4_TYG/MHD:HA or rga4_TYG/MHD:CFP or mock inoculation as negative controls. Pictures were taken 3 d (A) or 5 d (B and C) after infiltration. Equivalent results were obtained in three independent experiments.