| Literature DB >> 7737116 |
M Schönbächler1, A Horvath, J Fassler, H Riezman.
Abstract
The protein encoded by the yeast gene SPT14 shows high sequence similarity to the human protein, PIG-A, whose loss of activity is at the origin of the disease paroxysmal nocturnal hemoglobinuria. The symptoms of this disease are apparently due to a loss of cell surface, glycosylphosphatidylinositol (GPI)-anchored proteins. Like PIG-A mutant cells, spt14 mutant cells are defective in GPI anchoring due to a defect in the synthesis of GlcNAc-PI, the first step of GPI synthesis. The spt14 mutant causes several other abnormalities including transcriptional defects and a downregulation of inositolphosphoceramide synthesis. We suggest that these defects are indirect results of the loss of GPI anchoring.Entities:
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Year: 1995 PMID: 7737116 PMCID: PMC398256 DOI: 10.1002/j.1460-2075.1995.tb07152.x
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598