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- W3015540888 endingPage "160" @default.
- W3015540888 startingPage "139" @default.
- W3015540888 abstract "Focusing on the discovery and characterization of the Arabidopsis disease resistance protein RPS5 and its guardee PBS1, this review discusses work done in the Innes laboratory from the initial identification of the RPS5 gene in 1995 to the recent deployment of the PBS1 decoy system in crops. This is done through discussion of the structure, function, and signaling environment of RPS5 and PBS1, highlighting collaborations and influential ideas along the way. RPS5, a nucleotide-binding leucine-rich repeat (NLR) protein, is activated by the proteolytic cleavage of PBS1. We have shown that the cleavage site within PBS1 can be altered to contain cleavage sites for other proteases, enabling RPS5 activation by these proteases, thereby conferring resistance to different pathogens. This decoy approach has since been translated into crop species using endogenous PBS1 orthologs and holds strong potential for GMO-free development of new genetic resistance against important crop pathogens." @default.
- W3015540888 created "2020-04-17" @default.
- W3015540888 creator A5069476826 @default.
- W3015540888 creator A5083662273 @default.
- W3015540888 date "2020-08-25" @default.
- W3015540888 modified "2023-09-25" @default.
- W3015540888 title "RPS5-Mediated Disease Resistance: Fundamental Insights and Translational Applications" @default.
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