2011
DOI: 10.1016/j.biochi.2011.04.006
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Involvement of putative glutamate receptors in plant defence signaling and NO production

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Cited by 67 publications
(73 citation statements)
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References 32 publications
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“…The NO-induced Pro accumulation was a result of enhanced Pro synthesis and decreased degradation in maize (Yang and Gong, 2009). Although a relationship between the NO and the Pro precursor Glu was found in tobacco cells, where the involvement of a Glu-receptor in NO production and plant defence signalling was observed (Vatsa et al, 2011), the pattern of saltand NO-dependent changes for Pro and Glu was not similar in maize in the present experiment. This difference can be explained by the possible simultaneous use of Glu for Pro, GSH and/or polyamine synthesis.…”
Section: Gene Expression Studiescontrasting
confidence: 77%
“…The NO-induced Pro accumulation was a result of enhanced Pro synthesis and decreased degradation in maize (Yang and Gong, 2009). Although a relationship between the NO and the Pro precursor Glu was found in tobacco cells, where the involvement of a Glu-receptor in NO production and plant defence signalling was observed (Vatsa et al, 2011), the pattern of saltand NO-dependent changes for Pro and Glu was not similar in maize in the present experiment. This difference can be explained by the possible simultaneous use of Glu for Pro, GSH and/or polyamine synthesis.…”
Section: Gene Expression Studiescontrasting
confidence: 77%
“…Interestingly, it is possible that glutamate itself is a GLR-activating ligand (Chiu et al, 2002;Qi et al, 2006;Forde and Lea, 2007;Stephens et al, 2008). The fungal PAMP cryptogein can elicit an extracellular rise in glutamate and [Ca 2+ ] cyt that is driven by exocytosis (Vatsa et al, 2011), suggesting that glutamate release from the cell is downstream of PAMP perception (Weiland et al, 2016). This might provide a mechanism by which BAK1-mediated glutamate release could stimulate GLR activation.…”
Section: Discussionmentioning
confidence: 99%
“…Although DND1 is important for cytosolic Ca 2+ elevation in response to bacterial lipopolysaccharides and endogenous danger peptides (Ma et al, 2009;Qi et al, 2010), it is not required for flg22 and elf18 activation of Ca 2+ (Jeworutzki et al, 2010). Similarly, the recently suggested Glu receptor-like-type Ca 2+ channels have been implicated in cryptogein-and flg22-triggered responses by pharmacological approaches; however, genetic evidence for their involvement in MAMP signaling is still lacking (Kwaaitaal et al, 2011;Michard et al, 2011;Vatsa et al, 2011). Ca 2+ homeostasis is also controlled through the function of Ca 2+ ATPases, and our data show that FLS2 forms a complex with ACA8.…”
Section: Discussionmentioning
confidence: 99%
“…A number of ion channels have been identified, some of which have roles in plant immunity, such as DEFENSE NO DEATH1 (DND1; Clough et al, 2000;Lamotte et al, 2004;Kudla et al, 2010). Recently, ionotropic Glu receptor-like proteins were shown to regulate Ca 2+ influx at the plasma membrane and were also implicated in MAMP-induced responses (Cho et al, 2009;Kwaaitaal et al, 2011;Michard et al, 2011;Vatsa et al, 2011), and an endoplasmic reticulum-localized P2A-type Ca 2+ ATPase was described to contribute to pathogen-induced cell death and to alter the MAMP-triggered Ca 2+ burst (Zhu et al, 2010). The relevance of the Ca 2+ influx in MAMPelicited responses is underlined by polysaccharides secreted from bacterial pathogens to chelate Ca 2+ in the apoplastic space (Aslam et al, 2008).…”
mentioning
confidence: 99%