Plant Physiol, September 2000, Vol. 124, pp. 47-58
Molecular Characterization of CYP73A9 and
CYP82A1 P450 Genes Involved in Plant Defense in
Pea1
Joy M.
Whitbred and
Mary A.
Schuler*
Department of Cell and Structural Biology, University of Illinois,
Urbana, Illinois 61801
Cytochrome P450 monooxygenases (P450s) mediate a wide range of
oxidative reactions involved in the biosynthesis of phenylpropanoids, terpenes, and alkaloids. Two pea (Pisum sativum) P450
cDNAs (CYP73A9v1, encoding trans-cinnamic acid
hydroxylase [t-CAH] in the core phenylpropanoid pathway,
and CYP82A1v1, possibly encoding an activity in a late branch of the phenylpropanoid pathway) have previously been described. Of three CYP73A9 genes now isolated, the
CYP73A9v1 gene is full-length with two introns at
positions conserved in other t-CAH genes, and the
CYP73A9v2 and CYP73A9v3 gene fragments
are 5'-truncated and lack introns. The full-length
CYP82A1v2 gene contains a single intron at an alternate
position. Nucleotide searches of the CYP73A9v1 and
CYP82A1v2 promoters have indicated that the regulatory
sequences for these early and late phenylpropanoid transcripts are
substantially different. The P-, L-, and H-boxes identified in white
light-, ultraviolet light-, and elicitor-induced footprints in early
phenylpropanoid promoters (phenylalanine ammonia lyase
[PAL], 4-coumarate coenzyme A:ligase
[4-CL], and chalcone synthase [CHS])
are conserved in the t-CAH promoter and are absent from
the CYP82A1v2 promoter. Both promoters contain TCA
motifs identified in stress-responsive promoters, box IV elements
identified in elicitor-responsive PAL and
CHS promoters, and spatially conserved wound-response
elements potentially coordinating regulation of these
wound-responsive promoters.
1
This work was supported by U.S. Department of
Agriculture Competitive Research Grants (grant nos. 94-37301-7748 and
98-35304-6683).
*
Corresponding author; e-mail maryschu{at}uiuc.edu; fax
217-244-1336.
© 2000 American Society of Plant Physiologists