Back to Search
Start Over
Selective Usage of Isozymes for Stress Response.
- Source :
-
ACS chemical biology [ACS Chem Biol] 2018 Nov 16; Vol. 13 (11), pp. 3059-3064. Date of Electronic Publication: 2018 Nov 08. - Publication Year :
- 2018
-
Abstract
- Isozymes are enzymes with similar sequences that catalyze the same reaction in a given species. In Saccharomyces cerevisiae, most isozymes have major isoforms with high expression levels and minor isoforms with little expression under normal growth conditions. In a proteomic study aimed at identifying yeast protein regulated by rapamycin, we found an interesting phenomenon, that, for several metabolic enzymes, the major isozymes are downregulated while the minor isozymes are upregulated. Through enzymological and biochemical studies, we demonstrate that a rapamycin-upregulated enolase isozyme (ENO1) favors gluconeogenesis and a rapamycin-upregulated alcohol dehydrogenase isozyme (ALD4) promotes the reduction of NAD <superscript>+</superscript> to NADH (instead of NADP <superscript>+</superscript> to NADPH). Gene deletion study in yeast showed that the ENO1 and ALD4 are important for yeast survival under less-favorable growth conditions. Therefore, our study highlights the different metabolic needs of cells under different conditions and how nature chooses different isozymes to fit the metabolic needs.
- Subjects :
- Aldehyde Dehydrogenase metabolism
Aldehyde Oxidoreductases metabolism
Gene Expression Regulation drug effects
Gluconeogenesis drug effects
Isoenzymes metabolism
NAD metabolism
Phosphopyruvate Hydratase metabolism
Proteomics methods
Saccharomyces cerevisiae enzymology
Saccharomyces cerevisiae Proteins metabolism
Aldehyde Dehydrogenase antagonists & inhibitors
Protein Kinase Inhibitors pharmacology
Proteome metabolism
Saccharomyces cerevisiae Proteins antagonists & inhibitors
Sirolimus pharmacology
Stress, Physiological drug effects
Transcription Factors antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1554-8937
- Volume :
- 13
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- ACS chemical biology
- Publication Type :
- Academic Journal
- Accession number :
- 30346689
- Full Text :
- https://doi.org/10.1021/acschembio.8b00767