SNARE-protein-mediated disease resistance at the plant cell wall

By N. Collins, H. Thordal-Christensen, Volker Lipka, S. Bau, E. Kombrink, J. Qiu, R. Hückelhoven, Monica Stein, A. Freialdenhoven, S. Somerville and 1 more. Nature, 2003

973 citations recorded by the source corpus.

Subfields: Cell Biology, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/a3507d82ebaebc2685130462e76e4de89591047f

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Citations in the corpus

Priming: getting ready for battle. (2006, background): “This is supported by the high degree of homology between the above-mentioned SNARE genes and tobacco 1066 / Molecular Plant-Microbe Interactions NtSyp121, an ABA-inducible SNARE gene (Collins et al. 2003; Leymann et al. 1999).”
Abscisic Acid and Callose: Team Players in Defence Against Pathogens? (2005, background): “Genetic screens for fungal pathogen resistance in Arabidopsis and barley identified two SNARE encoding genes, PEN1 and ROR2 (Collins et al., 2003).”
Proteomic Identification of S-Nitrosylated Proteins in Arabidopsis1[w] (2005, background): “Conformational changes of cytoskeleton components due to S-nitrosylation might be involved in directing vesicles loaded with toxic metabolites to the infection site and deflating the contents into the extracellular space (Collins et al., 2003).”
Fungal Pathogens: The Battle for Plant Infection (2006, background): “Indeed, these mutants permit, at high frequency, efficient entry of the non-adapted pathogens (Collins et al., 2003).”
The role of abscisic acid in plant-pathogen interactions. (2005, background): “Interestingly, SNAREs have repeatedly been implicated in ABA-dependent responses to abiotic stress and to pathogen resistance [55,56].”
Priming of induced plant defense responses (2009, background): “Mutations in the SNARE genes PENETRATION-1 (PEN1) (encoding syntaxin) and REQUIRED FOR mlo RESISTANCE-2 (ROR2) (Collins et al., 2003; Lipka et al., 2005) caused a partial loss of resistance at the level of the plant cell wall, resulting in a loss of ‘‘basal resistance’’ to the nonadapted parasites B”
Arabidopsis PEN3/PDR8, an ATP Binding Cassette Transporter, Contributes to Nonhost Resistance to Inappropriate Pathogens That Enter by Direct Penetration[W][OA] (2006, background): “…the PEN genes became known, allelism among the various mutants was confirmed by sequencing the appropriate gene (i.e., PEN1, PEN2, orPEN3). pen1-4 (Collins et al., 2003), pen2-3 (Lipka et al., 2005), pen3-1, and pen3-2 were recovered from this screen. pen3-1, like the pen1 and pen2 mutants,…”
Proteome profile and functional classification of proteins in Arabidopsis thaliana (Landsberg erecta) mature pollen (2006, background): “This protein has a role in vesicle-mediated transport and protein-mediated disease resistance (Collins et al. 2003).”
ABA Is an Essential Signal for Plant Resistance to Pathogens Affecting JA Biosynthesis and the Activation of Defenses in Arabidopsis[W] (2007, background): “We analyzed the susceptibility of nonhormonal defense-related mutants, including nonhost-related mutants (pen1 and pen2; Collins et al., 2003; Assaad et al., 2004), mutants affected in responses to biotrophs (edr1, pad4, and eds1; Frye and Innes, 1998; Falk et al., 1999; Jirage et al., 1999), and…”
Roles of reactive oxygen species in interactions between plants and pathogens (2008, background): “Collins et al. (2003) showed that H2O2 was associated with vesicles containing cell wall components which were in transit to CWA, suggesting that H2O2 may play a role upstream of CWA or that compounds of CWA are oxidatively cross-linked on the way to the site of deposition.”