GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.

Have any questions? Please email us at ecoliwiki@gmail.com

PMID:19033156

From GONUTS
Jump to: navigation, search
Citation

Eanes, WF, Merritt, TJ, Flowers, JM, Kumagai, S and Zhu, CT (2009) Direct evidence that genetic variation in glycerol-3-phosphate and malate dehydrogenase genes (Gpdh and Mdh1) affects adult ethanol tolerance in Drosophila melanogaster. Genetics 181:607-14

Abstract

Many studies of alcohol adaptation in Drosophila melanogaster have focused on the Adh polymorphism, yet the metabolic elimination of alcohol should involve many enzymes and pathways. Here we evaluate the effects of glycerol-3-phosphate dehydrogenase (Gpdh) and cytosolic malate dehydrogenase (Mdh1) genotype activity on adult tolerance to ethanol. We have created a set of P-element-excision-derived Gpdh, Mdh1, and Adh alleles that generate a range of activity phenotypes from full to zero activity. Comparisons of paired Gpdh genotypes possessing 10 and 60% normal activity and 66 and 100% normal activity show significant effects where higher activity increases tolerance. Mdh1 null allele homozygotes show reductions in tolerance. We use piggyBac FLP-FRT site-specific recombination to create deletions and duplications of Gpdh. Duplications show an increase of 50% in activity and an increase of adult tolerance to ethanol exposure. These studies show that the molecular polymorphism associated with GPDH activity could be maintained in natural populations by selection related to adaptation to alcohols. Finally, we examine the interactions between activity genotypes for Gpdh, Mdh1, and Adh. We find no significant interlocus interactions. Observations on Mdh1 in both Gpdh and Adh backgrounds demonstrate significant increases in ethanol tolerance with partial reductions (50%) in cytosolic MDH activity. This observation strongly suggests the operation of pyruvate-malate and, in particular, pyruvate-citrate cycling in adaptation to alcohol exposure. We propose that an understanding of the evolution of tolerance to alcohols will require a system-level approach, rather than a focus on single enzymes.

Links

PubMed PMC2644950 Online version:10.1534/genetics.108.089383

Keywords

Alcohol Dehydrogenase/deficiency; Alcohol Dehydrogenase/genetics; Alcohol Dehydrogenase/metabolism; Alleles; Animals; Biological Evolution; Crosses, Genetic; Drosophila melanogaster/drug effects; Drosophila melanogaster/enzymology; Drosophila melanogaster/genetics; Drug Tolerance/genetics; Ethanol/metabolism; Ethanol/toxicity; Female; Gene Deletion; Gene Duplication; Genes, Insect; Genetic Variation; Glycerolphosphate Dehydrogenase/deficiency; Glycerolphosphate Dehydrogenase/genetics; Glycerolphosphate Dehydrogenase/metabolism; Malate Dehydrogenase/deficiency; Malate Dehydrogenase/genetics; Malate Dehydrogenase/metabolism; Male; Selection, Genetic

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

DROME:GPDA

GO:0006067: ethanol metabolic process

ECO:0000315:

P

Figure 2 shows increased lethality with gene deletion and increased survival with gene duplication

complete
CACAO 6596

DROME:GPDA

involved_in

GO:0006067: ethanol metabolic process

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete


See also

References

See Help:References for how to manage references in GONUTS.