TY - JOUR
T1 - Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair
AU - De La Concepcion, Juan Carlos
AU - Vega Benjumea, Javier
AU - Bialas, Aleksandra
AU - Terauchi, Ryohei
AU - Kamoun, Sophien
AU - Banfield, Mark J.
N1 - Acknowledgements: We thank present and former members of the Banfield and Kamoun laboratories for discussions that have shaped this manuscript, and colleagues at Iwate Biotechnology Research Center for stimulating discussions on NLR biology. We specially thank Dr. Cristina Barragan and Dr. Adam Bentham for critical reading of the manuscript. We also thank Andrew Davies and Phil Robinson from JIC Scientific Photography for the UV pictures of the cell death assays.
Funding Information: This work was supported by the Biotechnology and Biological Sciences Research Council (BBSRC, UK, grant BB/012574, BBS/E/J/000PR9795), the BBSRC Doctoral Training Partnership at Norwich Research Park (grant: BB/M011216/1, project reference 1771322), the European Research Council (proposal 743165), the John Innes Foundation, the Gatsby Charitable Foundation, the European Commission through the Erasmus+ programme, and JSPS Grant 20H05681.
PY - 2021/11/16
Y1 - 2021/11/16
N2 - Cooperation between receptors from the nucleotide-binding, leucine-rich repeats (NLR) superfamily is important for intracellular activation of immune responses. NLRs can function in pairs that, upon pathogen recognition, trigger hypersensitive cell death and stop pathogen invasion. Natural selection drives specialization of host immune receptors towards an optimal response, whilst keeping a tight regulation of immunity in the absence of pathogens. However, the molecular basis of co-adaptation and specialization between paired NLRs remains largely unknown. Here, we describe functional specialization in alleles of the rice NLR pair Pik that confers resistance to strains of the blast fungus Magnaporthe oryzae harbouring AVR-Pik effectors. We revealed that matching pairs of allelic Pik NLRs mount effective immune responses, whereas mismatched pairs lead to autoimmune phenotypes, a hallmark of hybrid necrosis in both natural and domesticated plant populations. We further showed that allelic specialization is largely underpinned by a single amino acid polymorphism that determines preferential association between matching pairs of Pik NLRs. These results provide a framework for how functionally linked immune receptors undergo co-adaptation to provide an effective and regulated immune response against pathogens. Understanding the molecular constraints that shape paired NLR evolution has implications beyond plant immunity given that hybrid necrosis can drive reproductive isolation.
AB - Cooperation between receptors from the nucleotide-binding, leucine-rich repeats (NLR) superfamily is important for intracellular activation of immune responses. NLRs can function in pairs that, upon pathogen recognition, trigger hypersensitive cell death and stop pathogen invasion. Natural selection drives specialization of host immune receptors towards an optimal response, whilst keeping a tight regulation of immunity in the absence of pathogens. However, the molecular basis of co-adaptation and specialization between paired NLRs remains largely unknown. Here, we describe functional specialization in alleles of the rice NLR pair Pik that confers resistance to strains of the blast fungus Magnaporthe oryzae harbouring AVR-Pik effectors. We revealed that matching pairs of allelic Pik NLRs mount effective immune responses, whereas mismatched pairs lead to autoimmune phenotypes, a hallmark of hybrid necrosis in both natural and domesticated plant populations. We further showed that allelic specialization is largely underpinned by a single amino acid polymorphism that determines preferential association between matching pairs of Pik NLRs. These results provide a framework for how functionally linked immune receptors undergo co-adaptation to provide an effective and regulated immune response against pathogens. Understanding the molecular constraints that shape paired NLR evolution has implications beyond plant immunity given that hybrid necrosis can drive reproductive isolation.
UR - http://www.scopus.com/inward/record.url?scp=85120889026&partnerID=8YFLogxK
U2 - 10.7554/eLife.71662
DO - 10.7554/eLife.71662
M3 - Article
VL - 10
JO - eLife
JF - eLife
SN - 2050-084X
M1 - e71662
ER -