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J. Biol. Chem., Vol. 263, Issue 19, 9155-9161, Jul, 1988
The yeast SEC53 gene encodes phosphomannomutase
F Kepes and R Schekman
Department of Biochemistry, University of California, Berkeley 94720.
Yeast sec53 cells incubated at a restrictive temperature (37 degrees C)
accumulate inactive and incompletely glycosylated forms of secretory
proteins within the lumen of the endoplasmic reticulum. A defect in
glycosylation of alpha-factor precursor has been reproduced in vitro using
membranes and cytosol isolated from sec53 mutant cells. Normal
glycosylation is restored in reactions supplemented with a cytosolic
fraction from wild type cells, with GDP-mannose, or with mannose 1-
phosphate and GTP, but not with mannose 6-phosphate and GTP. This pattern
of stimulation suggests that extracts of sec53 cells are deficient in
phosphomannomutase activity or in the production of a precursor of mannose
1-phosphate. Several lines of evidence demonstrate that SEC53 encodes the
yeast phosphomannomutase. Direct assay of soluble fractions from
independent alleles of sec53 shows low to negligible phosphomannomutase,
but nearly normal levels of phosphomannoisomerase activity. The residual
phosphomannomutase activity in mutant cell lysates is thermolabile in
proportion to the severity of the sec53 cell growth defect. Introduction of
the SEC53 gene on a multicopy plasmid into sec53 or wild type yeast and
into Salmonella typhimurium results in an increase in phosphomannomutase
activity that correlates with elevated expression of the Sec53 protein.
Finally, the Sec53 protein and phosphomannomutase activity cofractionate
exactly in a 70-fold partial purification involving gel filtration and DEAE
chromatography. The secretory defect in sec53 cells may now be explained by
a deficit in GDP-mannose production.

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Copyright © 1988 by the American Society for Biochemistry and Molecular Biology.
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