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Enzyme
Compound
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Target Concepts:
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Query: EC:3.2.1.31 (
beta-glucuronidase
)
7,680
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Mevalonate kinase
(
MVK
), the enzyme that catalyzes the phosphorylation of mevalonate to produce mevalonate 5-phosphate, is considered as a potential regulatory enzyme of the isoprenoid biosynthetic pathway. The Arabidopsis thaliana
MVK
gene corresponding to the
MVK
cDNA previously isolated has been cloned and characterized. RNAse protection analysis indicated that the expression of the
MVK
gene generates three mRNA populations with 5' ends mapping 203, 254 and 355 nt upstream of the
MVK
ATG start codon. Northern blot analysis showed that the
MVK
mRNA accumulates preferentially in roots and influorescences. Histochemical analysis, with transgenic A. thaliana plants containing a translational fusion of a 1.8 kb fragment of the 5' region of the
MVK
gene to the
beta-glucuronidase
(GUS) reporter gene, indicated that the
MVK
5'-flanking region directs widespread expression of the GUS gene throughout development, although the highest levels of GUS activity are detected in roots (meristematic region) and flowers (sepals, petals, anthers, style and stigmatic papillae). The expression pattern of the
MVK
gene suggests that the role of the encoded
MVK
is the production of a general pool of mevalonate-5-phosphate for the synthesis of different classes of isoprenoids involved in both basic and specialized plant cell functions. Functional promoter deletion analysis in transfected A. thaliana protoplasts indicated that regulatory elements between positions -295 and -194 of the
MVK
5'-flanking region are crucial for high-level
MVK
gene expression.
...
PMID:Molecular cloning and expression analysis of the mevalonate kinase gene from Arabidopsis thaliana. 1079 36