Perception of the bacterial PAMP EF-Tu by the receptor EFR restricts Agrobacterium-mediated transformation.
By Cyril Zipfel, Gernot Kunze, D. Chinchilla, A. Caniard, Jonathan D. G. Jones, T. Boller, G. Felix. Cell, 2006
1,934 citations recorded by the source corpus.
Subfields: Plant Science
View Paper: https://www.semanticscholar.org/paper/f921ed2830a701b4f89a2f78135f0b2bd370220d
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Plant Science
- Cyril Zipfel
- M. B. Bitonti
- Maria Greco
- A. Chiappetta
- L. Bruno
- P. Bakker
- Heribert Hirt
- L. C. van Loon
Citations in the corpus
- Elicitors, effectors, and R genes: the new paradigm and a lifetime supply of questions. (2007, methodology): “FLS2 and EFR1 respond to entirely different MAMPs yet both activate very similar plant defense responses (197).”
- Plant immunity: towards an integrated view of plant–pathogen interactions (2010, background): “Although the PAMP concept encompasses the idea that all PAMPs should be recognized by all species, this has been found to not always be the case, as perception of the bacterial elongation factor EF-Tu is apparently restricted to the Brassicacea”
- A receptor-like cytoplasmic kinase, BIK1, associates with a flagellin receptor complex to initiate plant innate immunity (2009, methodology): “One gene identified in this way was BIK1, whichwas rapidly induced byflg22 andEF-Tu treatments (21, 22).”
- Roles of Protein Synthesis Elongation Factor EF-Tu in Heat Tolerance in Plants (2012, background): “The innate immunity of the plant cells induces an oxidative burst and ethylene production and results in resistance to subsequent infection of pathogenic microbes [57, 58].”
- The Arabidopsis Leucine-Rich Repeat Receptor–Like Kinases BAK1/SERK3 and BKK1/SERK4 Are Required for Innate Immunity to Hemibiotrophic and Biotrophic Pathogens[W] (2011, methodology): “The expression of >1000 genes is altered within 30min of flg22 or elf18 treatment (Zipfel et al., 2004, 2006).”
- Impact of root exudates and plant defense signaling on bacterial communities in the rhizosphere. A review (2011, background): “Early signaling in recognition of flg22 and EF-Tu by FLS2 and EFR involves calcium-associated membrane anion channel opening (Jeworutzki et al. 2010).”
- Signaling mechanisms in pattern-triggered immunity (PTI). (2015, background): “acid long eliciting epitope called elf18 from Escherichia coli (Zipfel et al., 2006).”
- MAPK cascade signalling networks in plant defence. (2009, background): “Moreover, elf18 and flg22 induce an overlapping set of responses, including extracellular alkalisation, a rapid activation of MAPKs and the induction of similar response genes [27 ].”
- Growth-defense tradeoffs in plants: a balancing act to optimize fitness. (2014, neutral): “Due to space constraints, we focus our discussion on tradeoffs between defenses mediated by pathogen-associated-molecular-pattern (PAMP)-triggered immunity (PTI), salicylic acid (SA), and jasmonate (JA) versus growth mediated by auxin, brassinosteroids (BR), and gibberellins (GA), for which most pro”
- A domain swap approach reveals a role of the plant wall-associated kinase 1 (WAK1) as a receptor of oligogalacturonides (2010, methodology): “2A), confirming previous observations that Arabidopsis EFR is functional in tobacco (32).”