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PMID: 18359845 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

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

Plant physiology ·Vol. 147 ·No. 1 ·2008-05-00 ·Pages 415-28

Wentzell AM, Kliebenstein DJ

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.

MeSH Terms
Age Factors Arabidopsis/genetics,metabolism,physiology Arabidopsis Proteins/genetics,metabolism Environment Enzymes/metabolism Flowers/metabolism Genetic Variation Glucosinolates/chemistry,metabolism Glycoside Hydrolases/genetics,metabolism Molecular Structure Nitriles/metabolism Plant Leaves/metabolism Plant Roots/metabolism Population Density Seedlings/metabolism
Chemicals
Arabidopsis Proteins ESM1 protein, Arabidopsis Enzymes Glucosinolates Nitriles epithiospecifier protein, Arabidopsis Glycoside Hydrolases TGG1 protein, Arabidopsis TGG2 protein, Arabidopsis thioglucosidase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wentzell Adam M
Genetics Graduate Group and Department of Plant Sciences, University of California, Davis, Davis, CA 95616, USA.
Kliebenstein Daniel J
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Article Info
Journal
Plant physiology
Abbr.
Plant Physiol
ISSN
0032-0889
Published
2008-05-00
Epub
2008-00-21
Pages
415-28
Language
English
Region
United States
NLM ID
0401224
PMCID
PMC2330308
Subset
IM
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