Literature DB >> 8132653

Cloning and molecular characterization of three genes, including two genes encoding serine hydroxymethyltransferases, whose inactivation is required to render yeast auxotrophic for glycine.

J B McNeil1, E M McIntosh, B V Taylor, F R Zhang, S Tang, A L Bognar.   

Abstract

The genes encoding both the cytosolic and mitochondrial serine hydroxymethyltransferases (SHM2 and SHM1, respectively) and a third unidentified gene of the yeast Saccharomyces cerevisiae have been isolated and their nucleotide sequences determined. Analysis of the predicted amino acid sequence of the amino-terminal regions, sequence comparison with other genes encoding SHMT enzymes, and subcellular fractionation studies all suggested that the SHM1 gene encodes the mitochondrial SHMT, while the SHM2 gene encodes the cytosolic enzyme. The SHM2 gene but not the SHM1 gene has putative GCN4 sites upstream of the putative TATA box, suggesting regulation of its transcription by the general amino acid control system. Yeast mutants with disruptions at each SHM gene and in both genes were constructed and all mutants had the same growth requirements as the parental strains. Mutagenesis of the double-disrupted, shm1 shm2 yeast yielded strains of a single complementation group that are auxotrophic for glycine. Complementation of the glycine auxotrophy using a yeast genomic library retrieved the SHM1 and SHM2 genes and a third gene designated GLY1. Gene disruption studies demonstrated that inactivation of SHM1, SHM2, and GLY1 is required to yield yeast that are completely auxotrophic for glycine.

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Year:  1994        PMID: 8132653

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


  28 in total

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3.  Disruption of the SHM2 gene, encoding one of two serine hydroxymethyltransferase isoenzymes, reduces the flux from glycine to serine in Ashbya gossypii.

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Journal:  Biochem J       Date:  2003-01-15       Impact factor: 3.857

4.  Aspartate-Derived Amino Acid Biosynthesis in Arabidopsis thaliana.

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Journal:  Arabidopsis Book       Date:  2009-06-10

5.  Two Arabidopsis threonine aldolases are nonredundant and compete with threonine deaminase for a common substrate pool.

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6.  Network identification and flux quantification in the central metabolism of Saccharomyces cerevisiae under different conditions of glucose repression.

Authors:  A K Gombert; M Moreira dos Santos ; B Christensen; J Nielsen
Journal:  J Bacteriol       Date:  2001-02       Impact factor: 3.490

7.  Mice have a transcribed L-threonine aldolase/GLY1 gene, but the human GLY1 gene is a non-processed pseudogene.

Authors:  Alasdair J Edgar
Journal:  BMC Genomics       Date:  2005-03-09       Impact factor: 3.969

8.  Threonine aldolase overexpression plus threonine supplementation enhanced riboflavin production in Ashbya gossypii.

Authors:  N Monschau; H Sahm; K Stahmann
Journal:  Appl Environ Microbiol       Date:  1998-11       Impact factor: 4.792

9.  Evolution of threonine aldolases, a diverse family involved in the second pathway of glycine biosynthesis.

Authors:  Guangxiu Liu; Manxiao Zhang; Ximing Chen; Wei Zhang; Wei Ding; Qi Zhang
Journal:  J Mol Evol       Date:  2015-02-03       Impact factor: 2.395

10.  13C-metabolic flux ratio and novel carbon path analyses confirmed that Trichoderma reesei uses primarily the respirative pathway also on the preferred carbon source glucose.

Authors:  Paula Jouhten; Esa Pitkänen; Tiina Pakula; Markku Saloheimo; Merja Penttilä; Hannu Maaheimo
Journal:  BMC Syst Biol       Date:  2009-10-29
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