Chicken 11beta-hydroxysteroid dehydrogenase type 2: partial cloning and tissue distribution
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18201738
DOI
10.1016/j.steroids.2007.11.006
PII: S0039-128X(07)00219-X
Knihovny.cz E-resources
- MeSH
- 11-beta-Hydroxysteroid Dehydrogenase Type 2 genetics metabolism MeSH
- Cloning, Molecular MeSH
- DNA, Complementary metabolism MeSH
- Chickens genetics metabolism MeSH
- RNA, Messenger metabolism MeSH
- Molecular Sequence Data MeSH
- Avian Proteins genetics metabolism MeSH
- Amino Acid Sequence MeSH
- Base Sequence MeSH
- Sequence Alignment MeSH
- Tissue Distribution MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 11-beta-Hydroxysteroid Dehydrogenase Type 2 MeSH
- DNA, Complementary MeSH
- RNA, Messenger MeSH
- Avian Proteins MeSH
NAD(+)-dependent 11beta-hydroxysteroid dehydrogenase (11HSD2) converts glucocorticoids to 11-oxo derivatives and thus decreases their local concentration and prevents them from activating corticosteroid receptors. In this paper we report the partial cloning, characterization and tissue distribution of chicken 11HSD2. A cDNA of 991bp was cloned from kidney mRNA by reverse transcription and polymerase chain reaction. At the amino acid level, the sequence of PCR product had 56-59% homology with mammalian and 46-48% with fish 11HSD2. The consensus sequences of the short-chain dehydrogenase/reductase superfamily such as the catalytic activity motif Tyr-X-X-X-Lys and cosubstrate-binding motif Gly-X-X-X-Gly-X-Gly, were found in the cloned cDNA. Analysis of the tissue expression of chicken 11HSD2 mRNA and NAD(+)-dependent 11beta-oxidase activity showed a similar tissue distribution pattern in the majority of tissues. High levels of expression and activity were found in kidney, small intestine, colon and oviduct; low in ovary and almost zero in brain, liver and testis.
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