The Lec5 glycosylation mutant links homeobox genes with cholesterol and lipid-linked oligosaccharides

Author:

Lu Hua1,Sathe Adwait Amod2,Xing Chao234,Lehrman Mark A1

Affiliation:

1. Department of Pharmacology, UT Southwestern Medical Center, 6001 Forest Park Rd., Dallas, TX, USA

2. Eugene McDermott Center for Human Growth & Development, UT Southwestern Medical Center, 6001 Forest Park Rd., Dallas, TX, USA

3. Department of Bioinformatics, UT Southwestern Medical Center, 6001 Forest Park Rd., Dallas, TX, USA

4. Department of Clinical Sciences, UT Southwestern Medical Center, 6001 Forest Park Rd., Dallas, TX, USA

Abstract

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.

Funder

National Institutes of Health

M.A.L., C.X.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry

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