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PLANT PHYSIOLOGY , Vol 113, Issue 3 755-763, Copyright © 1997 by American Society of Plant Biologists
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GENE REGULATION AND MOLECULAR GENETICS |
Isolation of a cDNA and a Genomic Clone Encoding Cinnamate 4-Hydroxylase from Arabidopsis and Its Expression Manner in Planta
M. Mizutani, D. Ohta and R. Sato
International Research Laboratories, Ciba-Geigy Japan Ltd., 10-66 Miyuki-cho, Takarazuka 665, Japan
We have isolated a cDNA for a cytochrome P450, cinnamate 4-hydroxylase
(C4H), of Arabidopsis thaliana using a C4H cDNA from mung bean as a
hybridization probe. The deduced amino acid sequence is 84.7% identical to
that of mung bean C4H and therefore was designated CYP73A5. The CYP73A5
protein was expressed in insect cells using the baculovirus expression
system and when reconstituted with lipid and NADPH-cytochrome P450
reductase resulted in C4H activity with a specific activity of 68 nmol
min-1 nmol-1 P450. Southern blot analysis revealed that CYP73A5 is a
single-copy gene in Arabidopsis. C4H (CYP73A5) expression was apparently
coordinated in Arabidopsis with both PAL1 and 4CL in response to light and
wounding. Although the light induction of CHS followed a time course
similar to that observed with C4H, no induction of CHS was detected upon
wounding. On the other hand, the C4H expression patterns exhibited no
significant coordination with those of PAL2 and PAL3. A C4H promoter region
of 907 bp contained all of the three cis-acting elements (boxes P, A, and
L) conserved among the PAL and 4CL genes so far reported as controlling
expression.
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