RGD Reference Report - Novel members of the human oxysterol-binding protein family bind phospholipids and regulate vesicle transport. - Rat Genome Database

RGD Reference Report - Novel members of the human oxysterol-binding protein family bind phospholipids and regulate vesicle transport. - Rat Genome Database

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Novel members of the human oxysterol-binding protein family bind phospholipids and regulate vesicle transport.
Authors:	Xu, Y Liu, Y Ridgway, ND McMaster, CR
Citation:	Xu Y, etal., J Biol Chem 2001 May 25;276(21):18407-14.
RGD ID:	724388
Pubmed:	PMID:11279184 (View Abstract at PubMed)
DOI:	DOI:10.1074/jbc.M101204200 (Journal Full-text)
Oxysterol-binding proteins (OSBPs) are a family of eukaryotic intracellular lipid receptors. Mammalian OSBP1 binds oxygenated derivatives of cholesterol and mediates sterol and phospholipid synthesis through as yet poorly undefined mechanisms. The precise cellular roles for the remaining members of the oxysterol-binding protein family remain to be elucidated. In yeast, a family of OSBPs has been identified based on primary sequence similarity to the ligand binding domain of mammalian OSBP1. Yeast Kes1p, an oxysterol-binding protein family member that consists of only the ligand binding domain, has been demonstrated to regulate the Sec14p pathway for Golgi-derived vesicle transport. Specifically, inactivation of the KES1 gene resulted in the ability of yeast to survive in the absence of Sec14p, a phosphatidylinositol/phosphatidylcholine transfer protein that is normally required for cell viability due to its essential requirement in transporting vesicles from the Golgi. We cloned the two human members of the OSBP family, ORP1 and ORP2, with the highest degree of similarity to yeast Kes1p. We expressed ORP1 and ORP2 in yeast lacking Sec14p and Kes1p function and found that ORP1 complemented Kes1p function with respect to cell growth and Golgi vesicle transport, whereas ORP2 was unable to do so. Phenotypes associated with overexpression of ORP2 in yeast were a dramatic decrease in cell growth and a block in Golgi-derived vesicle transport distinct from that of ORP1. Purification of ORP1 and ORP2 for ligand binding studies demonstrated ORP1 and ORP2 did not bind 25-hydroxycholesterol but instead bound phospholipids with both proteins exhibiting strong binding to phosphatidic acid and weak binding to phosphatidylinositol 3-phosphate. In Chinese hamster ovary cells, ORP1 localized to a cytosolic location, whereas ORP2 was associated with the Golgi apparatus, consistent with our vesicle transport studies that indicated ORP1 and ORP2 function at different steps in the regulation of vesicle transport.

Objects referenced in this article

Gene	Osbpl1a	oxysterol binding protein-like 1A	Rattus norvegicus

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