phytosterols and 2-3-oxidosqualene

phytosterols has been researched along with 2-3-oxidosqualene* in 2 studies

Reviews

1 review(s) available for phytosterols and 2-3-oxidosqualene

ArticleYear
Brassinosteroids. Plant counterparts to animal steroid hormones?
    Vitamins and hormones, 2002, Volume: 65

    Brassinosteroids are polyhydroxylated derivatives of common plant membrane sterols such as campesterol. They occur throughout the plant kingdom and have been shown by genetic and biochemical analyses to be essential for normal plant growth and development. Numerous reviews have detailed the recent progress in our understanding of the biosynthesis, physiological responses, and molecular modes of action of brassinosteroids. It is clear that like their animal steroid counterparts, brassinosteroids have a defined receptor, can regulate the expression of specific genes, and can orchestrate complex physiological responses involved in growth. This review summarizes the current status of BR research, pointing out where appropriate the similarities and differences between the mechanism of action of brassinosteroids and the more thoroughly studied animal steroid hormones.

    Topics: Animals; Brassinosteroids; Cell Differentiation; Cell Division; Cholestanols; Cholesterol; Mevalonic Acid; Phytosterols; Plants; Signal Transduction; Squalene; Steroids; Steroids, Heterocyclic; Triterpenes

2002

Other Studies

1 other study(ies) available for phytosterols and 2-3-oxidosqualene

ArticleYear
Lanosterol synthase in dicotyledonous plants.
    Plant & cell physiology, 2006, Volume: 47, Issue:5

    Sterols are important as structural components of plasma membranes and precursors of steroidal hormones in both animals and plants. Plant sterols show a wide structural variety and significant structural differences from those of animals. To elucidate the origin of structural diversity in plant sterols, their biosynthesis has been extensively studied [Benveniste (2004) Annu. Rev. Plant. Biol. 55: 429, Schaller (2004) Plant Physiol. Biochem. 42: 465]. The differences in the biosynthesis of sterols between plants and animals begin at the step of cyclization of 2,3-oxidosqualene, which is cyclized to lanosterol in animals and to cycloartenol in plants. However, here we show that plants also have the ability to synthesize lanosterol directly from 2,3-oxidosqualene, which may lead to a new pathway to plant sterols. The Arabidopsis gene At3g45130, designated LAS1, encodes a functional lanosterol synthase in plants. A phylogenetic tree showed that LAS1 belongs to the previously uncharacterized branch of oxidosqualene cyclases, which differs from the cycloartenol synthase branch. Panax PNZ on the same branch was also shown to be a lanosterol synthase in a yeast heterologous expression system. The higher diversity of plant sterols may require two biosynthetic routes in steroidal backbone formation.

    Topics: Amino Acid Sequence; Arabidopsis; Arabidopsis Proteins; DNA, Plant; Gene Expression Regulation, Plant; Genes, Plant; Intramolecular Transferases; Lanosterol; Magnoliopsida; Molecular Sequence Data; Nuclear Proteins; Panax; Phylogeny; Phytosterols; Saccharomyces cerevisiae Proteins; Squalene

2006