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Updated: Feb 3, 2026

Analysis of SCAP N-glycosylation and Trafficking in Human Cells
Published on: November 8, 2016
The Lec5 glycosylation mutant links homeobox genes with cholesterol and lipid-linked oligosaccharides
Hua Lu1, Adwait Amod Sathe2, Chao Xing2,3,4
1Department of Pharmacology, UT Southwestern Medical Center, 6001 Forest Park Rd., Dallas, TX, USA.
Abstract:
Discovered 40 years ago, the Lec5 glycosylation mutant cell line has a complex recessive genotype and is characterized by accumulation of lipid-linked oligosaccharide assembly intermediates, reduced conversion of polyprenols to dolichols, and an unusual phenotypic dependence upon cell culture conditions such as temperature, plating density and medium quality. The heritable defect in Lec5 is unknown. Here we demonstrate an unexpected epigenetic basis for Lec5, with a surprising linkage to increased expression of homeobox genes, which in turn is associated with increased transcription of cholesterol biosynthesis genes. These results suggest testable hypotheses for the biochemical abnormalities of the Lec5 mutant.
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