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J. Biol. Chem., Vol. 255, Issue 22, 10752-10757, Nov, 1980

mRNA-dependent regulation of UDP-apiose synthase activity in irradiated plant cells

SE Gardiner, J Schroder, U Matern, D Hammer and K Hahlbrock

Large changes in the rate of synthesis of UDP-apiose synthase, an enzyme of the flavonoid glycoside pathway, were observed both in vivo and in vitro following irradiation of previously dark-grown cell suspension cultures of parsley (Petroselinum hortense). Irradiation of the cells with ultraviolet light for 2 1/2 h caused a large increase in UDP-adipose synthase mRNA activity which continued for several hours during the subsequent dark period. A sharp peak in this activity was followed by a rapid exponential decline. The timing of changes in mRNA activity was very similar for UDP-apiose synthase and chalcone synthase, a previously investigated enzyme of the flavonoid glycoside pathway, but differed from that for phenylalanine ammonia-lyase, an enzyme of general phenylpropanoid metabolism. Thus, the present data provide further evidence for a differential regulation of the two groups of enzymes and a high degree of co-ordination within each group. The expected light-induced changes in UDP-apiose synthase activity were calculated from the observed changes in the rate of synthesis, allowing for an apparently constant rate of degradation (t 1/2 = 17 h). The resulting time course was in agreement with experimental data, suggesting that the changes in enzyme activity were caused by corresponding changes in the rate of synthesis. A protein of unknown function (Protein X), which is tightly associated with UDP-apiose synthase and co-purifies with the enzyme at a molar ratio of 1:1, is shown to be regulated independently of the enzymes of the flavonoid glycoside pathway.
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Proc. Natl. Acad. Sci. USAHome page
E. Logemann, A. Tavernaro, W. Schulz, I. E. Somssich, and K. Hahlbrock
UV light selectively coinduces supply pathways from primary metabolism and flavonoid secondary product formation in parsley
PNAS, February 15, 2000; 97(4): 1903 - 1907.
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