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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1999-1-15
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pubmed:databankReference | |
pubmed:abstractText |
A cDNA of tobacco BY-2 cells corresponding to an mRNA species which was rapidly induced by methyl jasmonate (MeJA) in the presence of cycloheximide (CHX) was found to encode ornithine decarboxylase (ODC). Another cDNA from a MeJA-inducible mRNA encoded S-adenosylmethionine synthase (SAMS). Although these enzymes could be involved in the biosynthesis of polyamines, the level of putrescine, a reaction product of ODC, increased slowly and while the levels of spermidine and spermine did not change following treatment of cells with MeJA. However, N-methylputrescine, which is a precursor of pyrrolidine ring of nicotine, started to increase shortly after MeJA-treatment of cells and the production of nicotine occured thereafter. The levels of mRNA for arginine decarboxylase (ADC), an alternative enzyme for putrescine synthesis, and that for S-adenosylmethionine decarboxylase (SAMDC), required for polyamine synthesis, were not affected by MeJA. In addition to mRNAs for ODC and SAMS, mRNA for putrescine N-methyltransferase (PMT) was also induced by MeJA. Unlike the MeJA-induction of ODC mRNA, MeJA-induction of SAMS and PMT mRNAs were blocked by CHX. The level of ODC mRNA declined after 1 to 4 h following MeJA treatment, while the levels of mRNAs for SAMS and PMT continued to increase. Auxin significantly reduced the MeJA-inducible accumulation of mRNAs for ODC, SAMS and PMT. These results indicate that MeJA sequentially induces expression of a series of genes involved in nicotine biosynthesis by multiple regulatory mechanisms.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclopentanes,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Nicotine,
http://linkedlifedata.com/resource/pubmed/chemical/Ornithine Decarboxylase,
http://linkedlifedata.com/resource/pubmed/chemical/Oxylipins,
http://linkedlifedata.com/resource/pubmed/chemical/Plant Growth Regulators,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/methyl jasmonate
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0167-4412
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
38
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1101-11
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9869416-Acetic Acids,
pubmed-meshheading:9869416-Amino Acid Sequence,
pubmed-meshheading:9869416-Base Sequence,
pubmed-meshheading:9869416-Cells, Cultured,
pubmed-meshheading:9869416-Cyclopentanes,
pubmed-meshheading:9869416-DNA, Complementary,
pubmed-meshheading:9869416-DNA Primers,
pubmed-meshheading:9869416-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:9869416-Gene Expression Regulation, Plant,
pubmed-meshheading:9869416-Molecular Sequence Data,
pubmed-meshheading:9869416-Nicotine,
pubmed-meshheading:9869416-Ornithine Decarboxylase,
pubmed-meshheading:9869416-Oxylipins,
pubmed-meshheading:9869416-Plant Growth Regulators,
pubmed-meshheading:9869416-Plants, Toxic,
pubmed-meshheading:9869416-RNA, Messenger,
pubmed-meshheading:9869416-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:9869416-Sequence Alignment,
pubmed-meshheading:9869416-Sequence Homology, Amino Acid,
pubmed-meshheading:9869416-Tobacco,
pubmed-meshheading:9869416-Transcription, Genetic
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pubmed:year |
1998
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pubmed:articleTitle |
Differential induction by methyl jasmonate of genes encoding ornithine decarboxylase and other enzymes involved in nicotine biosynthesis in tobacco cell cultures.
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pubmed:affiliation |
Laboratory of Biochemistry, Graduate School of Bioagricultural Sciences Nagoya University, Chikusa, Japan.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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