Inhibition of shoot branching by new terpenoid plant hormones

By Mikihisa Umehara, A. Hanada, S. Yoshida, K. Akiyama, Tomotsugu Arite, Noriko Takeda-Kamiya, H. Magome, Y. Kamiya, K. Shirasu, K. Yoneyama and 2 more. Nature, 2008

1,962 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Plant Science

View Paper: https://www.semanticscholar.org/paper/611a7c1adfc278403079efb6d5a2c8f80b509e36

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In Ecology, Evolution, Behavior and Systematics

In Plant Science

Citations in the corpus

The strigolactone story. (2010, background): “Indeed, the ccd8 mutants of pea (rms1) and rice (d10) did not produce detectable levels of SLs, and in addition their excessive branching phenotypes could be rescued by the application of the synthetic SL GR24 (Figure 6b) (46, 128).”
Mechanisms underlying beneficial plant-fungus interactions in mycorrhizal symbiosis. (2010, background): “Strigolactones also have a hormonal role in inhibiting lateral branching of shoot”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “SLs are a novel class of plant hormones involved in controlling shoot branching inhibition (Gomez-Roldan et al., 2008; Umehara et al., 2008).”
Chrysanthemum Biotechnology: Quo vadis? (2013, background): “Strigolactones (SLs) have the ability of inhibiting bud activity but this depends on the presence of a competing auxin source (Umehara et al., 2008).”
The role of strigolactones in host specificity of Orobanche and Phelipanche seed germination (2010, background): “Strigolactones are apocarotenoids that regulate shoot branching (Gómez-Roldán et al., 2008; Umehara et al., 2008) and are exuded by host roots, serving in mycorrhizal symbiosis to branch the mycelium toward the host root (Akiyama et al., 2005).”
DWARF27, an Iron-Containing Protein Required for the Biosynthesis of Strigolactones, Regulates Rice Tiller Bud Outgrowth[W][OA] (2009, background): “Furthermore, application of strigolactones inhibits shoot branching in the ccd mutants of pea, rice, and Arabidopsis, but it has no effect on rms4/max2/d3 signaling mutants (Gomez-Roldan et al., 2008; Umehara et al., 2008 ).”
Phytohormones and their metabolic engineering for abiotic stress tolerance in crop plants (2016, positive): “Application of GR24, a synthetic and biologically active SL [94,95], repressed lateral root formation in wild-type seedlings and SL-synthesis mutants ( max3 and max4 ) but not in the strigolactone-response mutant ( max2 ), suggesting the MAX2 -dependent negative effect of strigolactone on lateral…”
Carotenoid metabolism in plants. (2015, neutral): “, 2003), while CCD7 and CCD8 are involved in the production of strigolactones (Gomez-Roldan et al., 2008; Umehara et al., 2008; Alder et al., 2012; Ruyter-Spira et al., 2013) via the synthesis of carlactone from b-carotene (Alder et al.”
Karrikins: A new family of plant growth regulators in smoke (2009, neutral): “thaliana [39,40].”
Arbuscular mycorrhiza: the mother of plant root endosymbioses (2008, background): “The recent pioneering discovery of strigolactones as novel endogenous plant hormones in diverse angiosperms that range from Arabidopsis thaliana to pea and ric”
Travel advice on the road to carotenoids in plants. (2010, background): “Carotenoids are important ubstrates for a class of cleavage dioxygenases that are responible for the synthesis of phytohormone apocarotenoids such as bscisic acid [19] and the recently discovered hormone strigolacone [20,21].”