Crosstalk between cytosolic and plastidial pathways of isoprenoid biosynthesis in Arabidopsis thaliana

By Oliver Laule, A. Fürholz, Hur-Song Chang, Tong Zhu, Xun Wang, P. Heifetz, Wilhelm Gruissem, M. Lange. Proceedings of the National Academy of Sciences of the United States of America, 2003

686 citations recorded by the source corpus.

Subfields: Biochemistry, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/2b6298b19adaea9cebbe13e36da1db0e5ca412fa

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Citations in the corpus

Hydrogen isotope fractionation in freshwater and marine algae: II. Temperature and nitrogen limited growth rate effects (2009, background): “Laule et al. (2003) provided indirect support for the presence of such an export mechanism in the vascular plant Arabidopsis thaliana.”
Early Steps in Isoprenoid Biosynthesis: Multilevel Regulation of the Supply of Common Precursors in Plant Cells (2006, methodology): “Since the complete block of the MEP pathway in Arabidopsis null mutants with defective MEP pathway genes leads to downregulated expression of MEP pathway genes (Laule et al., 2003; Guevara-Garcı́a et al., 2005), it is possible that a moderate decrease in the level of some isoprenoid metabolites pref”
Metabolic Engineering of Terpenoid Biosynthesis in Plants (2006, background): “In recent years several studies showed that transport of terpenoid precursors occurs between subcellular compartments (McCaskill and Croteau, 1998; Bick and Lange, 2003; Hemmerlin et al., 2003; Laule et al., 2003; Schuhr et al., 2003; Dudareva et al., 2005).”
Regularized rank-based estimation of high-dimensional nonparanormal graphical models (2012, background): “The selected models support the biological arguments that the interactions be-tween the pathways do exist although they operate independently under normal conditions [Laule et al. (2003), Rodr´ıguez-Concepci´on et al. (2004)].”
Sparse graphical Gaussian modeling of the isoprenoid gene network in Arabidopsis thaliana (2004, background): “Although both pathways operate independently under normal conditions, interaction between them has been repeatedly reported [16,17].”
A unified mechanism of action for volatile isoprenoids in plant abiotic stress. (2009, background): “The two pathways can be linked through exchange of metabolic precursors across the plastid membran”
Advances in Fruit Aroma Volatile Research (2013, background): “However, cross-talk between these two IPP biosynthetic pathways is prevalent, particularly in the direction from plastids to cytosol [153,154].”
The Strigolactone Germination Stimulants of the Plant-Parasitic Striga and Orobanche spp. Are Derived from the Carotenoid Pathway1 (2005, background): “Both compounds have been demonstrated to be quite efficiently inhibiting the cytosolic or plastidic isoprenoid biosynthetic pathway, respectively (Laule et al., 2003); hence, we might expect a clear effect of fosmidomycin, which in principle should also block carotenoid biosynthesis.”
Genes, enzymes and chemicals of terpenoid diversity in the constitutive and induced defence of conifers against insects and pathogens. (2006, background): “However, recent studies have revealed a sesquiterpene synthase in the plastid (Aharoni et al., 2004), and also plastid-derived IPP crossing over to the cytosol (Laule et al., 2003; Dudareva et al., 2005).”
Isoprene emission from plants: why and how. (2007, background): “It was originally assumed that the mevalonic acid pathway was the source of substrate (Sharkey et al., 1991; Sanadze, 2004), but it was demonstrated that a newly discovered pathway for making isoprenoids was the real source (Zeidler et al., 1997).”
Light-dependent regulation of carotenoid biosynthesis in plants (2009, background): “Crosstalk exists between the cytosolic and the plastidial pathways of isoprenoid biosynthesis, such that plastidial IPP can be exported to the cytosol (Rodríguez-Concepción and Gruissem, 1999; Laule et al., 2003).”
Biosynthesis of essential oils in aromatic plants: A review (2016, methodology): “It leads to the terpenes produced in plastids that can be partially derived from the intermediates of cytosolic mevalonate pathway and vice versa.((33,35))”
The iridoid pathway in Catharanthus roseus alkaloid biosynthesis (2007, background): “First, a few cell suspensions and compact callus cluster cultures are known to respond to tryptophan and/or tryptamine additions by an increased accumulation of MIAs (Zenk et al. 1977; Krueger and Carew 1978 ; Z hao et al. 2001).”
Tanshinone production and isoprenoid pathways in Salvia miltiorrhiza hairy roots induced by Ag+ and yeast elicitor (2005, background): “012 In higher plants, terpenes or isoprenoids are synthesized via at least two different pathways, the mevalonate (MVA) pathway occurring in the cytosol and the non-MVA, 1-deoxy-D-xylulose 5-phosphate (DXP) pathway in the plastids of cell [4,5] (Fig.”