Literature DB >> 2657396

Intragenic revertants of yeast invertase variants with secretion-defective leader sequences.

D Preuss1, D Botstein.   

Abstract

Several secretion-defective variants of invertase from Saccharomyces cerevisiae were generated by replacement of the wild-type signal sequence codons with DNA fragments with random sequences. Strains encoding these proteins failed to grow on medium containing sucrose as the sole source of carbon. The invertase that was made in these strains was found to fractionate with soluble, cytoplasmic proteins, and indirect immunofluorescence confirmed that the mutant invertase was located throughout the cytoplasm. To define the defects in the secretion-defective leader sequences, we selected revertants by requiring growth on sucrose. Surprisingly, most of the reversion events consisted of point changes and duplications in the upstream noncoding portion of the gene. Each of these changes introduced several hydrophobic residues into the nonfunctional leader sequences, suggesting that the defective random leader peptides might simply lack adequate hydrophobicity to be effective signal peptides.

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Year:  1989        PMID: 2657396      PMCID: PMC362562          DOI: 10.1128/mcb.9.4.1452-1464.1989

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  35 in total

1.  Determination of enzymatic activity in polyacrylamide gels. I. Enzymes catalyzing the conversion of nonreducing substrates to reducing products.

Authors:  O Gabriel; S F Wang
Journal:  Anal Biochem       Date:  1969-03       Impact factor: 3.365

2.  Nucleotide sequence of the yeast SUC2 gene for invertase.

Authors:  R Taussig; M Carlson
Journal:  Nucleic Acids Res       Date:  1983-03-25       Impact factor: 16.971

3.  A simple method for displaying the hydropathic character of a protein.

Authors:  J Kyte; R F Doolittle
Journal:  J Mol Biol       Date:  1982-05-05       Impact factor: 5.469

4.  Secretory protein translocation across membranes-the role of the "docking protein'.

Authors:  D I Meyer; E Krause; B Dobberstein
Journal:  Nature       Date:  1982-06-24       Impact factor: 49.962

5.  Transformation of intact yeast cells treated with alkali cations.

Authors:  H Ito; Y Fukuda; K Murata; A Kimura
Journal:  J Bacteriol       Date:  1983-01       Impact factor: 3.490

6.  The secreted form of invertase in Saccharomyces cerevisiae is synthesized from mRNA encoding a signal sequence.

Authors:  M Carlson; R Taussig; S Kustu; D Botstein
Journal:  Mol Cell Biol       Date:  1983-03       Impact factor: 4.272

7.  An MF alpha 1-SUC2 (alpha-factor-invertase) gene fusion for study of protein localization and gene expression in yeast.

Authors:  S D Emr; R Schekman; M C Flessel; J Thorner
Journal:  Proc Natl Acad Sci U S A       Date:  1983-12       Impact factor: 11.205

8.  Two differentially regulated mRNAs with different 5' ends encode secreted with intracellular forms of yeast invertase.

Authors:  M Carlson; D Botstein
Journal:  Cell       Date:  1982-01       Impact factor: 41.582

9.  Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccharomyces cerevisiae.

Authors:  A E Adams; J R Pringle
Journal:  J Cell Biol       Date:  1984-03       Impact factor: 10.539

10.  Genes required for completion of import of proteins into the endoplasmic reticulum in yeast.

Authors:  S Ferro-Novick; W Hansen; I Schauer; R Schekman
Journal:  J Cell Biol       Date:  1984-01       Impact factor: 10.539

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  2 in total

1.  Efficiency and diversity of protein localization by random signal sequences.

Authors:  C A Kaiser; D Botstein
Journal:  Mol Cell Biol       Date:  1990-06       Impact factor: 4.272

2.  Overall signal sequence hydrophobicity determines the in vivo translocation efficiency of a herpesvirus glycoprotein.

Authors:  P Ryan; A Robbins; M Whealy; L W Enquist
Journal:  Virus Genes       Date:  1993-02       Impact factor: 2.332

  2 in total

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