The orphan nuclear receptor LXRα is positively and negatively regulated by distinct products of mevalonate metabolism
- 30 September 1997
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 94 (20), 10588-10593
- https://doi.org/10.1073/pnas.94.20.10588
Abstract
LXRalpha is an orphan member of the nuclear hormone receptor superfamily that displays constitutive transcriptional activity. We reasoned that this activity may result from the production of an endogenous activator that is a component of intermediary metabolism. The use of metabolic inhibitors revealed that mevalonic acid biosynthesis is required for LXRalpha activity. Mevalonic acid is a common metabolite used by virtually all eukaryotic cells. It serves as a precursor to a large number of important molecules including farnesyl pyrophosphate, geranylgeranyl pyrophosphate, cholesterol, and oxysterols. Inhibition of LXRalpha could be reversed by addition of mevalonic acid and certain oxysterols but not by other products of mevalonic acid metabolism. Surprisingly, the constitutive activity of LXRalpha was inhibited by geranylgeraniol, a metabolite of mevalonic acid. These findings suggest that LXRalpha may represent a central component of a signaling pathway that is both positively and negatively regulated by multiple products of mevalonate metabolism.Keywords
This publication has 46 references indexed in Scilit:
- Metabolism of Farnesol: Phosphorylation of Farnesol by Rat Liver Microsomal and Peroxisomal FractionsBiochemical and Biophysical Research Communications, 1997
- An oxysterol signalling pathway mediated by the nuclear receptor LXRαNature, 1996
- The RXR heterodimers and orphan receptorsCell, 1995
- Farnesol Is Utilized for Protein Isoprenylation and the Biosynthesis of Cholesterol in Mammalian CellsBiochemical and Biophysical Research Communications, 1995
- Utilization of Geranylgeraniol for Protein Isoprenylation in C6 Glial CellsBiochemical and Biophysical Research Communications, 1994
- Cholesterol side-chain cleavage by mitochondria from the human placenta. Studies using hydroxycholesterols as substratesThe Journal of Steroid Biochemistry and Molecular Biology, 1992
- Correlation among oxysterol potencies in the regulation of the degradation of 3-hydroxy-3-methylglutaryl CoA reductase, the repression of 3-hydroxy-3-methylglutaryl COA synthase and affinities for the oxysterol receptorBiochemical and Biophysical Research Communications, 1992
- Regulation of the mevalonate pathwayNature, 1990
- Studies on steroids. XLV. Synthesis of the four stereoisomers of 20,22-dihydroxycholesterol.CHEMICAL & PHARMACEUTICAL BULLETIN, 1977
- The isolation of crystalline 22R-hydroxycholesterol and 20α,22R-dihydroxycholesterol from bovine adrenalsBiochemical and Biophysical Research Communications, 1970