Literature DB >> 3025587

Expression of the Saccharomyces cerevisiae inositol-1-phosphate synthase (INO1) gene is regulated by factors that affect phospholipid synthesis.

J P Hirsch, S A Henry.   

Abstract

The INO1 gene of Saccharomyces cerevisiae encodes the regulated enzyme inositol-1-phosphate synthase, which catalyzes the first committed step in the synthesis of inositol-containing phospholipids. The expression of this gene was analyzed under conditions known to regulate phospholipid synthesis. RNA blot hybridization with a genomic clone for INO1 detected two RNA species of 1.8 and 0.6 kb. The abundance of the 1.8-kb RNA was greatly decreased when the cells were grown in the presence of the phospholipid precursor inositol, as was the enzyme activity of the synthase. Complementation analysis showed that this transcript encoded the INO1 gene product. The level of INO1 RNA was repressed 12-fold when the cells were grown in medium containing inositol, and it was repressed 33-fold when the cells were grown in the presence of inositol and choline together. The INO1 transcript was present at a very low level in cells containing mutations (ino2 and ino4) in regulatory genes unlinked to INO1 that result in inositol auxotrophy. The transcript was constitutively overproduced in cells containing a mutation (opi1) that causes constitutive expression of inositol-1-phosphate synthase and results in excretion of inositol. The expression of INO1 RNA was also examined in cells containing a mutation (cho2) affecting the synthesis of phosphatidylcholine. In contrast to what was observed in wild-type cells, growth of cho2 cells in medium containing inositol did not result in a significant decrease in INO1 RNA abundance. Inositol and choline together were required for repression of the INO1 transcript in these cells, providing evidence for a regulatory link between the synthesis of inositol- and choline-containing lipids. The level of the 0.6-kb RNA was affected, although to a lesser degree, by many of the same factors that influence INO1 expression.

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Year:  1986        PMID: 3025587      PMCID: PMC367077          DOI: 10.1128/mcb.6.10.3320-3328.1986

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


  33 in total

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Authors:  H Lehrach; D Diamond; J M Wozney; H Boedtker
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2.  Control of inositol biosynthesis in Saccharomyces cerevisiae: properties of a repressible enzyme system in extracts of wild-type (Ino+) cells.

Authors:  M R Culbertson; T F Donahue; S A Henry
Journal:  J Bacteriol       Date:  1976-04       Impact factor: 3.490

3.  A rapid alkaline extraction procedure for screening recombinant plasmid DNA.

Authors:  H C Birnboim; J Doly
Journal:  Nucleic Acids Res       Date:  1979-11-24       Impact factor: 16.971

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Authors:  D B Clewell; D R Helinski
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5.  Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.

Authors:  P S Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

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Authors:  M R Culbertson; S A Henry
Journal:  Genetics       Date:  1975-05       Impact factor: 4.562

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Authors:  T F Donahue; S A Henry
Journal:  J Biol Chem       Date:  1981-07-10       Impact factor: 5.157

8.  Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose.

Authors:  H Aviv; P Leder
Journal:  Proc Natl Acad Sci U S A       Date:  1972-06       Impact factor: 11.205

9.  A GAL10-CYC1 hybrid yeast promoter identifies the GAL4 regulatory region as an upstream site.

Authors:  L Guarente; R R Yocum; P Gifford
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

10.  Cloning of yeast gene for trichodermin resistance and ribosomal protein L3.

Authors:  H M Fried; J R Warner
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

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  91 in total

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Authors:  M Elkhaimi; M R Kaadige; D Kamath; J C Jackson; H Biliran; J M Lopes
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

2.  The REG1 gene product is required for repression of INO1 and other inositol-sensitive upstream activating sequence-containing genes of yeast.

Authors:  Q Ouyang; M Ruiz-Noriega; S A Henry
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

3.  Interruption of inositol sphingolipid synthesis triggers Stt4p-dependent protein kinase C signaling.

Authors:  Stephen A Jesch; Maria L Gaspar; Christopher J Stefan; Manuel A Aregullin; Susan A Henry
Journal:  J Biol Chem       Date:  2010-10-23       Impact factor: 5.157

4.  Analysis of sequences in the INO1 promoter that are involved in its regulation by phospholipid precursors.

Authors:  J M Lopes; J P Hirsch; P A Chorgo; K L Schulze; S A Henry
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

5.  Derepression of INO1 transcription requires cooperation between the Ino2p-Ino4p heterodimer and Cbf1p and recruitment of the ISW2 chromatin-remodeling complex.

Authors:  Ameet Shetty; John M Lopes
Journal:  Eukaryot Cell       Date:  2010-10-08

6.  The INO2 gene of Saccharomyces cerevisiae encodes a helix-loop-helix protein that is required for activation of phospholipid synthesis.

Authors:  D M Nikoloff; P McGraw; S A Henry
Journal:  Nucleic Acids Res       Date:  1992-06-25       Impact factor: 16.971

7.  Genomic analysis of the Opi- phenotype.

Authors:  Leandria C Hancock; Ryan P Behta; John M Lopes
Journal:  Genetics       Date:  2006-04-02       Impact factor: 4.562

8.  Characterization of the yeast DGK1-encoded CTP-dependent diacylglycerol kinase.

Authors:  Gil-Soo Han; Laura O'Hara; Symeon Siniossoglou; George M Carman
Journal:  J Biol Chem       Date:  2008-05-05       Impact factor: 5.157

9.  INO1-100: an allele of the Saccharomyces cerevisiae INO1 gene that is transcribed without the action of the positive factors encoded by the INO2, INO4, SWI1, SWI2 and SWI3 genes.

Authors:  S Swift; P McGraw
Journal:  Nucleic Acids Res       Date:  1995-04-25       Impact factor: 16.971

10.  Adenovirus E1A specifically blocks SWI/SNF-dependent transcriptional activation.

Authors:  M E Miller; B R Cairns; R S Levinson; K R Yamamoto; D A Engel; M M Smith
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