Literature DB >> 3392042

A Chinese hamster ovary cell mutant F2A8 utilizes polyprenol rather than dolichol for its lipid-dependent asparagine-linked glycosylation reactions.

J Stoll1, A G Rosenwald, S S Krag.   

Abstract

Previous results suggested that F2A8, a glycosylation mutant of Chinese hamster ovary cells, had a lower amount of dolichyl phosphate available for asparagine-linked glycosylation reactions relative to parental cells. The steady-state amounts and identities of polyisoprenoid lipids were determined by incubating F2A8, its parental cell line B4-2-1, and wild-type Chinese hamster ovary cells for 24 h with [2-3H]mevalonate. The neutral lipids, ubiquinone, cholesterol, and cholesteryl esters, which were the most highly labeled from [3H]mevalonate, were labeled equally in all three cell types. In wild-type and B4-2-1 cells, mevalonate incorporation into the anionic glycosylated and phosphorylated derivatives of dolichol was 10-fold higher than into the neutral free dolichol and dolichyl esters. In contrast, in F2A8 cells, label accumulated in neutral polyisoprenol lipids, so that the ratio of neutral to anionic lipids was 1:1 rather than 1:10. In wild-type and B4-2-1 cells, the polyisoprenoid found as free alcohol and in phosphorylated and glycosylated forms was shown by high pressure liquid chromatography using a silica column to be primarily dolichol, a polyisoprenol that has a saturated terminal isoprene unit. In contrast, in F2A8 cells the polyisoprenoid found primarily as the free alcohol and in phosphorylated and glycosylated forms appeared to be completely unsaturated polyprenol. The distribution of chain lengths of the labeled polyisoprenols of F2A8, B4-2-1, and wild-type cells was the same as determined by high pressure liquid chromatography using a reverse-phase column, with the predominant chain length being 19 isoprene units. These results combined with our previous studies on the phenotype of the F2A8 mutant indicate that the unsaturated polyprenyl phosphate derivatives do not function as well as dolichyl phosphate derivatives in cellular glycosylation reactions.

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Year:  1988        PMID: 3392042

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

1.  Saccharomyces cerevisiae sec59 cells are deficient in dolichol kinase activity.

Authors:  L Heller; P Orlean; W L Adair
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

2.  A 13-amino acid peptide in three yeast glycosyltransferases may be involved in dolichol recognition.

Authors:  C F Albright; P Orlean; P W Robbins
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

3.  MPDU1 regulates CEACAM1 and cell adhesion in vitro and in vivo.

Authors:  Daniel C Bennett; Aurelie Cazet; Jon Charest; Joseph N Contessa
Journal:  Glycoconj J       Date:  2018-04-18       Impact factor: 2.916

Review 4.  At the membrane frontier: a prospectus on the remarkable evolutionary conservation of polyprenols and polyprenyl-phosphates.

Authors:  Meredith D Hartley; Barbara Imperiali
Journal:  Arch Biochem Biophys       Date:  2011-11-10       Impact factor: 4.013

5.  Dolichol phosphate mannose synthase is required in vivo for glycosyl phosphatidylinositol membrane anchoring, O mannosylation, and N glycosylation of protein in Saccharomyces cerevisiae.

Authors:  P Orlean
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

6.  Control of carbohydrate processing: increased beta-1,6 branching in N-linked carbohydrates of Lec9 CHO mutants appears to arise from a defect in oligosaccharide-dolichol biosynthesis.

Authors:  A G Rosenwald; P Stanley; S S Krag
Journal:  Mol Cell Biol       Date:  1989-03       Impact factor: 4.272

7.  Dolichol biosynthesis in human malignant cells.

Authors:  A Henry; P W Stacpoole; C M Allen
Journal:  Biochem J       Date:  1991-09-15       Impact factor: 3.857

Review 8.  Structure and synthesis of polyisoprenoids used in N-glycosylation across the three domains of life.

Authors:  Meredith B Jones; Julian N Rosenberg; Michael J Betenbaugh; Sharon S Krag
Journal:  Biochim Biophys Acta       Date:  2009-04-05

9.  Metabolomics profiling reveals new aspects of dolichol biosynthesis in Plasmodium falciparum.

Authors:  Flavia M Zimbres; Ana Lisa Valenciano; Emilio F Merino; Anat Florentin; Nicole R Holderman; Guijuan He; Katarzyna Gawarecka; Karolina Skorupinska-Tudek; Maria L Fernández-Murga; Ewa Swiezewska; Xiaofeng Wang; Vasant Muralidharan; Maria Belen Cassera
Journal:  Sci Rep       Date:  2020-08-06       Impact factor: 4.379

  9 in total

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