MYC2 Differentially Modulates Diverse Jasmonate-Dependent Functions in Arabidopsis[W]

By B. Dombrecht, G. Xue, S. Sprague, J. Kirkegaard, J. Ross, J. B. Reid, G. Fitt, N. Sewelam, Peer Schenk, John Manners and 1 more. The Plant Cell Online, 2007

1,045 citations recorded by the source corpus.

Subfields: Insect Science, Plant Science

View Paper: https://www.semanticscholar.org/paper/104c9a7b9f59baf832ec039b4fb13c14d1b639f9

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In Insect Science

1. C. Wasternack
2. B. Hause
3. C. Pieterse
4. Susheng Song
5. Jonathan D. G. Jones
6. G. Howe
7. Rajendra Bari
8. J. Chico

In Plant Science

1. Kazuko Yamaguchi-Shinozaki
2. Kazuo Shinozaki
3. C. Wasternack
4. M. Fujita
5. Y. Fujita
6. C. Pieterse
7. Motoaki Seki
8. B. Hause

Citations in the corpus

• Role of plant hormones in plant defence responses (2009, background): “This indicates that MYC2 differentially regulates JA-responsive pathogen defence and wound response genes in Arabidopsis (Lorenzo and Solano 2005; Dombrecht et al. 2007).”
• ABA-mediated transcriptional regulation in response to osmotic stress in plants (2011, background): “2005), and 50-CACHTG-30 (Dombrecht et al. 2007), apparently indicating that the MYC2 core binding sequence is 50-CACNTG-30.”
• Regulation of Photosynthesis during Abiotic Stress-Induced Photoinhibition. (2015, neutral): “…Gossypium hirusitum dehydration-1355 responsive element binding protein 1 (Shan et al., 2007); JA, jasmonic acid; MYC 2, 1356 myelocytomatosis 2 TF (Dombrecht et al., 2007); PSI, photosystem I; PSII, photosystem II; ROS, 1357 reactive oxygen species; SA, salicylic acid; SL, strigolactone; SlZF2,…”
• Jasmonate Regulates the INDUCER OF CBF EXPRESSION–C-REPEAT BINDING FACTOR/DRE BINDING FACTOR1 Cascade and Freezing Tolerance in Arabidopsis[W] (2013, background): “…MYC3, and MYC4 function as direct targets of JAZ proteins to modulate a subset of jasmonate-regulated responses, such as the inhibition of root elongation and defense responses (Boter et al., 2004; Lorenzo et al., 2004; Chini et al., 2007; Dombrecht et al., 2007; FernándezCalvo et al., 2011).”
• Biosynthesis and biological functions of terpenoids in plants. (2015, background): “TPS21 and the second floral sesquiterpene synthase, TPS11 [187], also respond more directly to JA by the direct binding of their promoters to the bHLH transcription factor MYC2 [231], which is a central regulator of the JA signaling pathway in developmental and stress responses [232, 233].”
• Hormonal modulation of plant immunity. (2012, background): “Moreover, when the ERF branch was activated and the MYC branch suppressed by ORA59 overexpression, plants became more attractive to P. rapae larvae (Verhage et al. 2011).”
• Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. (2013, background): “This is supported by the fact that all the three MYC TFs show identical DNA binding specificities and bind preferentially to the G-box (Fernández-Calvo et al., 2011), the cis-element to which most bHLH proteins can potentially bind (Dombrecht et al., 2007).”
• Arabidopsis MYC2 Interacts with DELLA Proteins in Regulating Sesquiterpene Synthase Gene Expression[W][OA] (2012, background): “Previous in vitro and in vivo binding assays showed that MYC2 binds to the G-box cis-element (CACGTG) and G-box– like motifs (AACGTG or CATGTG) (Boter et al., 2004; Dombrecht et al., 2007; Hou et al., 2010).”
• Hormone crosstalk in plant disease and defense: more than just jasmonate-salicylate antagonism. (2011, background): “Exogenous JA application induces broad transcriptional reprogramming, a significant proportion of which is attributable to AtMYC2, a basic helix loop helix transcription factor and a key regulator of JA responses in plant-microbe interactions (49, 101, 113).”
• Ecological costs of biotrophic versus necrotrophic pathogen resistance, the hypersensitive response and signal transduction (2008, neutral): “2 gene and genes associated with production of anti-microbial defense metabolites such as indole glucosinolates and the phytoalexin camalexin [65-67].”
• The Arabidopsis bHLH Transcription Factors MYC3 and MYC4 Are Targets of JAZ Repressors and Act Additively with MYC2 in the Activation of Jasmonate Responses[C][W] (2011, background): “2 (Lorenzo et al., 2004; Dombrecht et al., 2007).”
• The JAZ Proteins: A Crucial Interface in the Jasmonate Signaling Cascade (2011, background): “Interestingly, the MYC2/MYC3/MYC4 complex is also involved in the JA-mediated induction of anthocyanin biosynthesis (Lorenzo et al., 2004; Dombrecht et al., 2007; Niu et al., 2011), but trichome induction seems to be independent of the MYC2 presence (Yoshida et al., 2009).”