Metabolic network analysis of the causes and evolution of enzyme dispensability in yeast
- PMID: 15190353
- DOI: 10.1038/nature02636
Metabolic network analysis of the causes and evolution of enzyme dispensability in yeast
Abstract
Under laboratory conditions 80% of yeast genes seem not to be essential for viability. This raises the question of what the mechanistic basis for dispensability is, and whether it is the result of selection for buffering or an incidental side product. Here we analyse these issues using an in silico flux model of the yeast metabolic network. The model correctly predicts the knockout fitness effects in 88% of the genes studied and in vivo fluxes. Dispensable genes might be important, but under conditions not yet examined in the laboratory. Our model indicates that this is the dominant explanation for apparent dispensability, accounting for 37-68% of dispensable genes, whereas 15-28% of them are compensated by a duplicate, and only 4-17% are buffered by metabolic network flux reorganization. For over one-half of those not important under nutrient-rich conditions, we can predict conditions when they will be important. As expected, such condition-specific genes have a more restricted phylogenetic distribution. Gene duplicates catalysing the same reaction are not more common for indispensable reactions, suggesting that the reason for their retention is not to provide compensation. Instead their presence is better explained by selection for high enzymatic flux.
Similar articles
-
Metabolic functions of duplicate genes in Saccharomyces cerevisiae.Genome Res. 2005 Oct;15(10):1421-30. doi: 10.1101/gr.3992505. Genome Res. 2005. PMID: 16204195 Free PMC article.
-
Rate of protein evolution versus fitness effect of gene deletion.Mol Biol Evol. 2003 May;20(5):772-4. doi: 10.1093/molbev/msg078. Epub 2003 Apr 2. Mol Biol Evol. 2003. PMID: 12679525
-
Exposing the fitness contribution of duplicated genes.Nat Genet. 2008 May;40(5):676-81. doi: 10.1038/ng.123. Epub 2008 Apr 13. Nat Genet. 2008. PMID: 18408719
-
Selection for more of the same product as a force to enhance concerted evolution of duplicated genes.Trends Genet. 2006 Dec;22(12):642-4. doi: 10.1016/j.tig.2006.09.014. Epub 2006 Oct 11. Trends Genet. 2006. PMID: 17045359 Review.
-
Retention of protein complex membership by ancient duplicated gene products in budding yeast.Trends Genet. 2007 Jun;23(6):266-9. doi: 10.1016/j.tig.2007.03.012. Epub 2007 Apr 10. Trends Genet. 2007. PMID: 17428571 Review.
Cited by
-
The metabolic domestication syndrome of budding yeast.Proc Natl Acad Sci U S A. 2024 Mar 12;121(11):e2313354121. doi: 10.1073/pnas.2313354121. Epub 2024 Mar 8. Proc Natl Acad Sci U S A. 2024. PMID: 38457520 Free PMC article.
-
Translation variation across genetic backgrounds reveals a post-transcriptional buffering signature in yeast.Nucleic Acids Res. 2024 Mar 21;52(5):2434-2445. doi: 10.1093/nar/gkae030. Nucleic Acids Res. 2024. PMID: 38261993 Free PMC article.
-
The Architecture of Metabolic Networks Constrains the Evolution of Microbial Resource Hierarchies.Mol Biol Evol. 2023 Sep 1;40(9):msad187. doi: 10.1093/molbev/msad187. Mol Biol Evol. 2023. PMID: 37619982 Free PMC article.
-
Evolutionary conservation of sequence motifs at sites of protein modification.J Biol Chem. 2023 May;299(5):104617. doi: 10.1016/j.jbc.2023.104617. Epub 2023 Mar 16. J Biol Chem. 2023. PMID: 36933807 Free PMC article.
-
Rapid Intraspecies Evolution of Fitness Effects of Yeast Genes.Genome Biol Evol. 2022 May 3;14(5):evac061. doi: 10.1093/gbe/evac061. Genome Biol Evol. 2022. PMID: 35482054 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials