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.2008 May;147(1):415-28.
doi: 10.1104/pp.107.115279. Epub 2008 Mar 21.

Genotype, age, tissue, and environment regulate the structural outcome of glucosinolate activation

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Genotype, age, tissue, and environment regulate the structural outcome of glucosinolate activation

Adam M Wentzell et al. Plant Physiol.2008 May.

Abstract

Glucosinolates are the inert storage form of a two-part phytochemical defense system in which the enzyme myrosinase generates an unstable intermediate that rapidly rearranges into the biologically active product. This rearrangement step generates simple nitriles, epithionitriles, or isothiocyanates, depending on the structure of the parent glucosinolate and the presence of proteins that promote specific structural outcomes. Glucosinolate accumulation and myrosinase activity differ by plant age and tissue type and respond to environmental stimuli such as planting density and herbivory; however, the influence of these factors on the structural outcome of the rearrangement step remains unknown. We show that the structural outcome of glucosinolate activation is controlled by interactions among plant age, planting density, and natural genetic variation in Arabidopsis (Arabidopsis thaliana) rosette leaves using six well-studied accessions. We identified a similarly complex interaction between tissue type and the natural genetic variation present within these accessions. This raises questions about the relative importance of these novel levels of regulation in the evolution of plant defense. Using mutants in the structural specifier and glucosinolate activation genes identified previously in Arabidopsis rosette leaves, we demonstrate the requirement for additional myrosinases and structural specifiers controlling these processes in the roots and seedlings. Finally, we present evidence for a novel EPITHIOSPECIFIER PROTEIN-independent, simple nitrile-specifying activity that promotes the formation of simple nitriles but not epithionitriles from all glucosinolates tested.

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Figures

Figure 1.
Figure 1.
Rearrangement during glucosinolate activation can generate multiple structural outcomes and mediate plant-herbivore interactions. A, Variable structural outcomes across plant development could optimize a plant's defensive chemistry to temporal changes in the herbivore community. The shaded triangles represent changing frequencies of two herbivores over the life of a plant. B, Tissue-dependent variation in herbivore communities may alter the regulation of metabolite diversity to optimize defense against a variety of feeding guilds, such as phloem-feeding aphids, leaf-chewing lepidopteran larvae, and root-feeding nematodes. C, Aggregated populations will produce more volatile metabolites than highly dispersed individuals, increasing the risk of detection and herbivory by adapted pests. This may select for modified volatile profiles in the presence of conspecific neighbors. D, Arabidopsis myrosinase initiates glucosinolate activation by hydrolyzing the thio-Glc bond, generating an unstable intermediate that rapidly rearranges into the biologically active structures. This intermediate will spontaneously rearrange into isothiocyanate structures. Structural specifiers alter this rearrangement in planta by enhancing the formation of specific structures. For example,ESP promotes the formation of epithionitriles and simple nitriles, whereasESM1 blocks the formation of simple nitrile and epithionitrile structures. Only glucosinolates with a terminal double bond can form all three structures.
Figure 2.
Figure 2.
Structural outcomes of glucosinolate activation in Col-0 rosettes as a function of age and growth conditions. Percentages of simple nitrile (white circles) and isothiocyanate (black triangles) were determined for both the exogenously supplied allyl glucosinolate and the endogenous 4-methylsulfinylbutyl glucosinolate (4MSO) at weekly intervals in the rosette leaves of Col-0. All time points are plotted as averages ±se. A, Structural outcomes for plants grown at low density (one plant per 49 cm2) plotted against the age of the plants. B, Structural outcomes for plants grown at high density (100 plants per 49 cm2).
Figure 3.
Figure 3.
Developmental trajectories of structural outcomes for six accessions. Structural outcomes were determined in rosette leaves, and the average percentages of simple nitrile (white circles), epithionitrile (black squares), and isothiocyanate (black triangles) for allyl glucosinolate activation are plotted against the age of the plants ±se. The Col-0 trajectories are reproduced to facilitate comparison. A, Structural outcomes for plants grown at low density (one plant per 49 cm2) plotted against the age of the plants. B, Structural outcomes for plants grown at high density (100 plants per 49 cm2).
Figure 4.
Figure 4.
Changes in structural outcomes in flowers and cauline leaves. Glucosinolate activation was assayed in flowers, cauline leaves, and rosette leaves using allyl glucosinolate in four plants of each accession. Average percentages of simple nitrile (dark shading), epithionitrile (light shading), and isothiocyanate (white) are shown. Accessions with a single asterisk showed significant differences between the flowers and leaves. Two asterisks indicate significant differences between flowers, cauline leaves, and rosette leaves. A, Structural outcomes in the flowers and inflorescences of accessions lacking functionalESP. B, Structural outcomes in the flowers and inflorescences of accessions with functionalESP. None of these three accessions showed significant differences in simple nitrile proportions between these tissues.
Figure 5.
Figure 5.
Structural outcomes in seedlings. Structural outcomes were measured using allyl glucosinolate in 3- and 7-d-old seedlings and are reported as average percentages of a given structure. The accessions are Bay-0 (♦), Col-0 (□) Mr-0 (▴), Cvi (○), Ler (*), and Sha (•). Significant changes between days within an accession are indicated by dashed lines. A, Percentage of simple nitrile in seedlings of all accessions. B, Percentage of epithionitrile in Cvi, Ler, and Sha seedlings. C, Percentage of isothiocyanate in seedlings of all accessions.
Figure 6.
Figure 6.
Structural outcomes in roots. The structural outcome of glucosinolate activation was assayed using allyl glucosinolate in the roots of 2-week-old plants. A, Representative gas chromatography-flame ionization detection chromatogram of glucosinolate activation products in Sha roots. No epithionitrile products were observed in the roots of any accession. B, Percentages of simple nitrile (dark shading) and isothiocyanate (white) are shown as averages ±se. Structural outcomes were also assayed in Col-0 and Ler roots using exogenous benzyl glucosinolate (Benzyl GS) as the substrate. The accessions producing significantly lower levels of simple nitriles relative to Col-0 are indicated by asterisks.
Figure 7.
Figure 7.
Structural outcomes in glucosinolate activation mutants. Structural outcomes were measured using allyl glucosinolate in the roots and seedlings of mutants with alterations in the myrosinases and structural specifier genes known to function in rosette leaves. See “Materials and Methods” for descriptions of each line. A, Percentage of simple nitrile (dark shading) in the seedlings of several mutants in the Col-0 background, lacking functionalESP (KO), reported as averages ±se, with the remainder of the activation products forming isothiocyanates (white). B, Average percentage of each structure ±se in seedlings overexpressing eitherESP in the Col-0 background orESM1 in the CS1995 background. The percentage of epithionitrile is shown in light shading. The accession Ler is included for comparison with CS1995, a homozygous line obtained from a cross between Ler and Col-0. C, Average percentage of simple nitrile in 2-week-old roots of these mutants and their wild-type (WT) backgrounds, shown ±se.
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References

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