Chapman Sean, Stevens Laura J, Boevink Petra C, Engelhardt Stefan, Alexander Colin J, Harrower Brian, Champouret Nicolas, McGeachy Kara, Van Weymers Pauline S M, Chen Xinwei, Birch Paul R J, Hein Ingo
Cell and Molecular Sciences, James Hutton Institute, Invergowrie-Dundee, United Kingdom.
Cell and Molecular Sciences, James Hutton Institute, Invergowrie-Dundee, United Kingdom; Division of Plant Sciences, University of Dundee at James Hutton Institute, Invergowrie-Dundee, United Kingdom; Dundee Effector Consortium, Invergowrie-Dundee, United Kingdom.
PLoS One. 2014 Oct 23;9(10):e110158. doi: 10.1371/journal.pone.0110158. eCollection 2014.
Engineering resistance genes to gain effector recognition is emerging as an important step in attaining broad, durable resistance. We engineered potato resistance gene R3a to gain recognition of the virulent AVR3aEM effector form of Phytophthora infestans. Random mutagenesis, gene shuffling and site-directed mutagenesis of R3a were conducted to produce R3a* variants with gain of recognition towards AVR3aEM. Programmed cell death following gain of recognition was enhanced in iterative rounds of artificial evolution and neared levels observed for recognition of AVR3aKI by R3a. We demonstrated that R3a*-mediated recognition responses, like for R3a, are dependent on SGT1 and HSP90. In addition, this gain of response is associated with re-localisation of R3a* variants from the cytoplasm to late endosomes when co-expressed with either AVR3aKI or AVR3aEM a mechanism that was previously only seen for R3a upon co-infiltration with AVR3aKI. Similarly, AVR3aEM specifically re-localised to the same vesicles upon recognition by R3a* variants, but not with R3a. R3a and R3a* provide resistance to P. infestans isolates expressing AVR3aKI but not those homozygous for AVR3aEM.
工程改造抗性基因以获得效应子识别能力正成为实现广泛、持久抗性的重要一步。我们对马铃薯抗性基因R3a进行了工程改造,使其能够识别致病疫霉的毒性效应子AVR3aEM。对R3a进行了随机诱变、基因改组和定点诱变,以产生对AVR3aEM具有识别能力增强的R3a变体。在人工进化的迭代轮次中,识别能力增强后的程序性细胞死亡得到了增强,接近R3a对AVR3aKI识别时所观察到的水平。我们证明,R3a介导的识别反应,与R3a一样,依赖于SGT1和HSP90。此外,这种反应增强与R3a变体在与AVR3aKI或AVR3aEM共表达时从细胞质重新定位到晚期内体有关,这一机制以前仅在R3a与AVR3aKI共浸润时才出现。同样,AVR3aEM在被R3a变体识别时特异性地重新定位到相同的囊泡,但与R3a共表达时则不会。R3a和R3a*对表达AVR3aKI的致病疫霉分离株具有抗性,但对AVR3aEM纯合的分离株则没有抗性。