The heat shock protein Ssa2p is required for import of fructose-1,6- bisphosphatase into Vid vesicles

C. Randell Brown, Jameson A. McCann, Hui Ling Chiang

Research output: Contribution to journalArticle

60 Citations (Scopus)

Abstract

Fructose-1,6-bisphosphatase (FBPase) is targeted to the vacuole for degradation when Saccharomyces cerevisiae are shifted from low to high glucose. Before vacuolar import, however, FBPase is sequestered inside a novel type of vesicle, the vacuole import and degradation (Vid) vesicles. Here, we reconstitute import of FBPase into isolated Vid vesicles. FBPase sequestration into Vid vesicles required ATP and cytosol, but was inhibited if ATP binding proteins were depleted from the cytosol. The heat shock protein Ssa2p was identified as one of the ATP binding proteins involved in FBPase import. A Δssa2 strain exhibited a significant decrease in the rate of FBPase degradation in vivo as compared with Δssa1, Δssa3, or Δssa4 strains. Likewise, in vitro import was impaired for the Δssa2 strain, but not for the other Δssa strains. The cytosol was identified as the site of the Δssa2 defect; Δssa2 cytosol did not stimulate FBPase import into import competent Vid vesicles, but wild-type cytosol supported FBPase import into competent Δssa2 vesicles. The addition of purified recombinant Ssa2p stimulated FBPase import into Δssa2 Vid vesicles; providing Δssa2 cytosol was present. Thus, Ssa2p, as well as other undefined cytosolic proteins are required for the import of FBPase into vesicles.

Original languageEnglish (US)
Pages (from-to)65-76
Number of pages12
JournalJournal of Cell Biology
Volume150
Issue number1
DOIs
StatePublished - Jul 10 2000

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Fructose-Bisphosphatase
Heat-Shock Proteins
Vacuoles
Cytosol
Adenosine Triphosphate
Carrier Proteins
Saccharomyces cerevisiae

All Science Journal Classification (ASJC) codes

  • Cell Biology

Cite this

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title = "The heat shock protein Ssa2p is required for import of fructose-1,6- bisphosphatase into Vid vesicles",
abstract = "Fructose-1,6-bisphosphatase (FBPase) is targeted to the vacuole for degradation when Saccharomyces cerevisiae are shifted from low to high glucose. Before vacuolar import, however, FBPase is sequestered inside a novel type of vesicle, the vacuole import and degradation (Vid) vesicles. Here, we reconstitute import of FBPase into isolated Vid vesicles. FBPase sequestration into Vid vesicles required ATP and cytosol, but was inhibited if ATP binding proteins were depleted from the cytosol. The heat shock protein Ssa2p was identified as one of the ATP binding proteins involved in FBPase import. A Δssa2 strain exhibited a significant decrease in the rate of FBPase degradation in vivo as compared with Δssa1, Δssa3, or Δssa4 strains. Likewise, in vitro import was impaired for the Δssa2 strain, but not for the other Δssa strains. The cytosol was identified as the site of the Δssa2 defect; Δssa2 cytosol did not stimulate FBPase import into import competent Vid vesicles, but wild-type cytosol supported FBPase import into competent Δssa2 vesicles. The addition of purified recombinant Ssa2p stimulated FBPase import into Δssa2 Vid vesicles; providing Δssa2 cytosol was present. Thus, Ssa2p, as well as other undefined cytosolic proteins are required for the import of FBPase into vesicles.",
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The heat shock protein Ssa2p is required for import of fructose-1,6- bisphosphatase into Vid vesicles. / Randell Brown, C.; McCann, Jameson A.; Chiang, Hui Ling.

In: Journal of Cell Biology, Vol. 150, No. 1, 10.07.2000, p. 65-76.

Research output: Contribution to journalArticle

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