Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:2.1.1.69 (BMT)
 2,655 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

We analyzed the developmental regulation and the activation by wounding of several stress-related genes in various parsley organs. The genes encode phenylalanine ammonia-lyase (PAL) and 4-coumarate:CoA ligase (4CL), two enzymes of general phenylpropanoid metabolism; a flavonoid specific enzyme, chalcone synthase (CHS); a furanocoumarin specific enzyme, bergaptol O-methyltransferase (BMT); and a pathogenesis-related protein (PR 1). All genes or gene families exhibited high levels of expression in roots and during certain stages of leaf development. PAL, 4CL and CHS were preferentially expressed in young leaves, BMT and PR 1 in old leaves. An appreciable increase in CHS mRNA levels was observed in wounded leaves. By contrast, root wounding led to a decrease in the existing CHS mRNA levels. A biphasic response (a decrease followed by an increase) to wounding was seen for BMT and PR 1 mRNAs in roots and for BMT mRNA in attached leaves. Using gene-specific oligonucleotide probes to measure the expression rates of three of the four PAL genes and of the two 4CL genes separately we observed a differential behavior of the individual family members under many of the conditions tested. While PAL-3 was preferentially activated in wounded leaves and 4CL-1 in wounded roots, PAL-2 and 4CL-2 were primarily responsible for the high constitutive expression levels in roots and flowering stems respectively. Despite the differential expression of their individual members, the PAL and 4CL gene families displayed very similar changes in the overall patterns of expression, reflecting their closely related functions in phenylpropanoid metabolism.
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PMID:Differential wound activation of members of the phenylalanine ammonia-lyase and 4-coumarate:CoA ligase gene families in various organs of parsley plants. 137 96

We analyzed the expression patterns of several pathogen defense-related genes in primary leaf buds of parsley by in situ RNA hybridization. Labeled antisense RNA probes were generated from seven selected cDNAs detecting transcripts from genes that are rapidly and strongly activated in cultured parsley cells upon treatment with fungal elicitor. These genes encode two enzymes of general phenylpropanoid metabolism, phenylalanine ammonia-lyase and 4-coumarate:CoA ligase, a furanocoumarin-specific bergaptol O-methyltransferase, one pathogenesis-related protein, and three less well characterized proteins, designated as ELI 3, ELI 5, and ELI 7. In uninfected tissue, phenylalanine ammonia-lyase and 4-coumarate:CoA ligase mRNA levels were high in epidermal cells, oil-duct epithelial cells, and cells of the developing xylem; bergaptol O-methyltransferase mRNA was confined to oil-duct epithelial cells; and the pathogenesis-related protein and ELI 3, ELI 5, and ELI 7 mRNAs were undetectable. All seven mRNAs accumulated transiently and locally around infection sites caused by the soybean-pathogenic fungus Phytophthora megasperma f. sp. glycinea, to which parsley is nonhost-resistant. The observed late appearance of bergaptol O-methyltransferase mRNA, as compared with all other mRNAs, is in accord with a similar relative timing of transient gene activation in elicitor-treated cell cultures. Sharp borders were observed between the infection center, where hypersensitive cell death had occurred in response to fungal penetration, the surrounding area of local gene activation, and the remainder of the tissue not showing any apparent response. Some of the genes were also activated, although less sharply localized, upon wounding of parsley leaves.
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PMID:Temporal and Spatial Patterns of Gene Expression around Sites of Attempted Fungal Infection in Parsley Leaves. 1235 83