E. Logemann et al., UV light selectively coinduces supply pathways from primary metabolism andflavonoid secondary product formation in parsley, P NAS US, 97(4), 2000, pp. 1903-1907
Citations number
33
Categorie Soggetti
Multidisciplinary
Journal title
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
The UV light-induced synthesis of UV-protective flavonoids diverts substant
ial amounts of substrates from primary metabolism into secondary product fo
rmation and thus causes major perturbations of the cellular homeostasis, Re
sults from this study show that the mRNAs encoding representative enzymes f
rom various supply pathways are coinduced in UV-irradiated parsley cells (P
etroselinum crispum) with two mRNAs of flavonoid glycoside biosynthesis, en
coding phenylalanine ammonia-lyase and chalcone synthase. Strong induction
was observed for mRNAs encoding glucose 6-phosphate dehydrogenase (carbohyd
rate metabolism, providing substrates for the shikimate pathway), 3-deoxyar
abinoheptulosonate 7-phosphate synthase (shikimate pathway, yielding phenyl
alanine), and acyl-CoA oxidase (fatty acid degradation, yielding acetyl-CoA
), and moderate induction for an mRNA encoding S-adenosyl-homocysteine hydr
olase (activated methyl cycle, yielding S-adenosyl-methionine for B-ring me
thylation). Ten arbitrarily selected mRNAs representing various unrelated m
etabolic activities remained unaffected. Comparative analysis of acyl-CoA o
xidase and chalcone synthase with respect to mRNA expression modes and gene
promoter structure and function revealed close similarities. These results
indicate a fine-tuned regulatory network integrating those functionally re
lated pathways of primary and secondary metabolism that are specifically re
quired for protective adaptation to UV irradiation. Although the response o
f parsley cells to UV light is considerably broader than previously assumed
, it contrasts greatly with the extensive metabolic reprogramming observed
previously in elicitor-treated or fungus-infected cells.