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PLANT PHYSIOLOGY , Vol 113, Issue 1 65-74, Copyright © 1997 by American Society of Plant Biologists
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GENE REGULATION AND MOLECULAR GENETICS |
Molecular Cloning of 4-Coumarate:Coenzyme A Ligase in Loblolly Pine and the Roles of This Enzyme in the Biosynthesis of Lignin in Compression Wood
X. H. Zhang and V. L. Chiang
Plant Biotechnology Research Center, School of Forestry and Wood Products, Michigan Technological University, Houghton, Michigan 49931
Two genomic sequences encoding 4-coumarate:coenzyme A ligase (4CL;EC
6.2.1.12) in loblolly pine (Pinus taeda L.) were cloned. Both sequences
contained three introns and four exons with identical coding sequences
predicting 537 amino acids. Two of the three introns in these two clones
were different both in sequence and in length. Sequences of both 4CL clones
were found in all nine megagametophyte DNAs tested, providing genetic
evidence that these two 4CL genomic sequences are nonallelic genes. Our
analyses suggest that there are at least two distinct, intron-containing
4CL genes, at least one of which is transcribed into 4CL mRNA in developing
xylem tissue of loblolly pine. The levels of 4CL gene transcription in
xylem were influenced by compressional stress, resulting in an elevated 4CL
enzyme activity with 4-coumaric acid. 4CL enzyme activity with ferulic acid
remained unchanged, whereas with caffeic acid it was significantly
inhibited. Exogenously applied trans-cinnamic acid in the protein extracts
from normal wood xylem caused inhibition of 4CL activity toward caffeic
acid similar to that under compressional stress. The implications of this
cinnamic acid-modulated effect on 4CL enzyme activities toward different
substrates in regulating monolignol synthesis in xylem under compressional
stress are discussed.
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