Epistatic Interaction Maps Relative to Multiple Metabolic Phenotypes
An epistatic interaction between two genes occurs when the phenotypic impact of one gene depends on another gene, often exposing a functional association between them. Due to experimental scalability and to evolutionary significance, abundant work has been focused on studying how epistasis affects cellular growth rate, most notably in yeast. However, epistasis likely influences many different phenotypes, affecting our capacity to understand cellular functions, biochemical networks adaptation, and genetic diseases. Despite its broad significance, the extent and nature of epistasis relative to different phenotypes remain fundamentally unexplored. Here we use genome-scale metabolic network modeling to investigate the extent and properties of epistatic interactions relative to multiple phenotypes. Specifically, using an experimentally refined stoichiometric model for Saccharomyces cerevisiae, we computed a three-dimensional matrix of epistatic interactions between any two enzyme gene deletions, with respect to all metabolic flux phenotypes. We found that the total number of epistatic interactions between enzymes increases rapidly as phenotypes are added, plateauing at approximately 80 phenotypes, to an overall connectivity that is roughly 8-fold larger than the one observed relative to growth alone. Looking at interactions across all phenotypes, we found that gene pairs interact incoherently relative to different phenotypes, i.e. antagonistically relative to some phenotypes and synergistically relative to others. Specific deletion-deletion-phenotype triplets can be explained metabolically, suggesting a highly informative role of multi-phenotype epistasis in mapping cellular functions. Finally, we found that genes involved in many interactions across multiple phenotypes are more highly expressed, evolve slower, and tend to be associated with diseases, indicating that the importance of genes is hidden in their total phenotypic impact. Our predictions indicate a pervasiveness of nonlinear effects in how genetic perturbations affect multiple metabolic phenotypes. The approaches and results reported could influence future efforts in understanding metabolic diseases and the role of biochemical regulation in the cell.
Vyšlo v časopise:
Epistatic Interaction Maps Relative to Multiple Metabolic Phenotypes. PLoS Genet 7(2): e32767. doi:10.1371/journal.pgen.1001294
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1001294
Souhrn
An epistatic interaction between two genes occurs when the phenotypic impact of one gene depends on another gene, often exposing a functional association between them. Due to experimental scalability and to evolutionary significance, abundant work has been focused on studying how epistasis affects cellular growth rate, most notably in yeast. However, epistasis likely influences many different phenotypes, affecting our capacity to understand cellular functions, biochemical networks adaptation, and genetic diseases. Despite its broad significance, the extent and nature of epistasis relative to different phenotypes remain fundamentally unexplored. Here we use genome-scale metabolic network modeling to investigate the extent and properties of epistatic interactions relative to multiple phenotypes. Specifically, using an experimentally refined stoichiometric model for Saccharomyces cerevisiae, we computed a three-dimensional matrix of epistatic interactions between any two enzyme gene deletions, with respect to all metabolic flux phenotypes. We found that the total number of epistatic interactions between enzymes increases rapidly as phenotypes are added, plateauing at approximately 80 phenotypes, to an overall connectivity that is roughly 8-fold larger than the one observed relative to growth alone. Looking at interactions across all phenotypes, we found that gene pairs interact incoherently relative to different phenotypes, i.e. antagonistically relative to some phenotypes and synergistically relative to others. Specific deletion-deletion-phenotype triplets can be explained metabolically, suggesting a highly informative role of multi-phenotype epistasis in mapping cellular functions. Finally, we found that genes involved in many interactions across multiple phenotypes are more highly expressed, evolve slower, and tend to be associated with diseases, indicating that the importance of genes is hidden in their total phenotypic impact. Our predictions indicate a pervasiveness of nonlinear effects in how genetic perturbations affect multiple metabolic phenotypes. The approaches and results reported could influence future efforts in understanding metabolic diseases and the role of biochemical regulation in the cell.
Zdroje
1. PhillipsPC
2008 Epistasis - the essential role of gene interactions in the structure and evolution of genetic systems. Nat Rev Genet 9 855 867
2. GuarenteL
1993 Synthetic enhancement in gene interaction: a genetic tool come of age. Trends Genet 9 362 366
3. SteinA
AloyP
A molecular interpretation of genetic interactions in yeast. FEBS Lett. In Press, Uncorrected Proof. Available at: http://www.sciencedirect.com/science/article/B6T36-4RW9H0W-9/2/65bd6932e8a94989a5767a584ec5a47d. Accessed 25 February 2008
4. SchuldinerM
CollinsSR
ThompsonNJ
DenicV
BhamidipatiA
2005 Exploration of the Function and Organization of the Yeast Early Secretory Pathway through an Epistatic Miniarray Profile. Cell 123 507 519
5. YeP
PeyserBD
PanX
BoekeJD
SpencerFA
2005 Gene function prediction from congruent synthetic lethal interactions in yeast. Mol Syst Biol 1 Available at: http://dx.doi.org/10.1038/msb4100034. Accessed 4 December 2008
6. SegrèD
DelunaA
ChurchGM
KishonyR
2005 Modular epistasis in yeast metabolism. Nat Genet 37 77 83
7. CostanzoM
BaryshnikovaA
BellayJ
KimY
SpearED
2010 The Genetic Landscape of a Cell. Science 327 425 431
8. ManiR
St OngeRP
HartmanJL
GiaeverG
RothFP
2008 Defining genetic interaction. Proc Natl Acad Sci U S A 105 3461 3466
9. KondrashovAS
1994 Muller's ratchet under epistatic selection. Genetics 136 1469 73
10. MazurkiewiczP
TangCM
BooneC
HoldenDW
2006 Signature-tagged mutagenesis: barcoding mutants for genome-wide screens. Nat Rev Genet 7 929 939
11. DeutscherD
MeilijsonI
KupiecM
RuppinE
2006 Multiple knockout analysis of genetic robustness in the yeast metabolic network. Nat Genet 38 993 998
12. HarrisonR
PappB
PalC
OliverSG
DelneriD
2007 Plasticity of genetic interactions in metabolic networks of yeast. Proc Natl Acad Sci U S A 104 2307 12
13. YehP
TschumiAI
KishonyR
2006 Functional classification of drugs by properties of their pairwise interactions. Nat Genet 38 489 494
14. TongAHY
LesageG
BaderGD
DingH
XuH
2004 Global Mapping of the Yeast Genetic Interaction Network. Science 303 808 813
15. ParsonsAB
BrostRL
DingH
LiZ
ZhangC
2004 Integration of chemical-genetic and genetic interaction data links bioactive compounds to cellular target pathways. Nat Biotechnol 22 62 69
16. ChaitR
CraneyA
KishonyR
2007 Antibiotic interactions that select against resistance. Nature 446 668 671
17. ElenaSF
LenskiRE
1997 Test of synergistic interactions among deleterious mutations in bacteria. Nature 390 395 398
18. JasnosL
KoronaR
2007 Epistatic buffering of fitness loss in yeast double deletion strains. Nat Genet 39 550 554
19. BremRB
StoreyJD
WhittleJ
KruglyakL
2005 Genetic interactions between polymorphisms that affect gene expression in yeast. Nature 436 701 703
20. St. OngeRP
ManiR
OhJ
ProctorM
FungE
2007 Systematic pathway analysis using high-resolution fitness profiling of combinatorial gene deletions. Nat Genet 39 199 206
21. CarlborgO
HaleyCS
2004 Epistasis: too often neglected in complex trait studies? Nat Rev Genet 5 618 625
22. CordellHJ
2009 Detecting gene-gene interactions that underlie human diseases. Nat Rev Genet 10 392 404
23. MooreJH
WilliamsSM
2009 Epistasis and Its Implications for Personal Genetics. Am J Hum Genet 85 309 320
24. KuepferL
SauerU
BlankLM
2005 Metabolic functions of duplicate genes in Saccharomyces cerevisiae. Genome Res 15 1421 1430
25. FörsterJ
FamiliI
PalssonBO
NielsenJ
2003 Large-scale evaluation of in silico gene deletions in Saccharomyces cerevisiae. OMICS 7 193 202
26. SnitkinE
DudleyA
JanseD
WongK
ChurchG
2008 Model-driven analysis of experimentally determined growth phenotypes for 465 yeast gene deletion mutants under 16 different conditions. Genome Biol 9 R140
27. DuarteNC
HerrgardMJ
PalssonBO
2004 Reconstruction and Validation of Saccharomyces cerevisiae iND750, a Fully Compartmentalized Genome-Scale Metabolic Model. Genome Res 14 1298 1309
28. HarrisonR
PappB
PalC
OliverSG
DelneriD
2007 Plasticity of genetic interactions in metabolic networks of yeast. Proc Natl Acad Sci U S A 104 2307 2312
29. SegrèD
VitkupD
ChurchGM
2002 Analysis of optimality in natural and perturbed metabolic networks. Proc Natl Acad Sci U S A 99 15112 15117
30. BlankL
KuepferL
SauerU
2005 Large-scale 13C-flux analysis reveals mechanistic principles of metabolic network robustness to null mutations in yeast. Genome Biol 6 R49
31. SnitkinES
SegrèD
2008 Optimality criteria for the prediction of metabolic fluxes in yeast mutants. Genome Informatics 2008 - Proceedings of the 8th Annual International Workshop on Bioinformatics and Systems Biology (IBSB 2008). Zeuten Lake, Berlin, Germany: 123 134 Available at: http://eproceedings.worldscinet.com/9781848163003/9781848163003_0011.html. Accessed 13 January 2010
32. WolfJB
BrodieED
WadeMJ
2000 Epistasis and the Evolutionary Process
33. OteroJ
OlssonL
NielsenJ
2008 Industrial Systems Biology of Saccharomyces cerecisiae: Succinic Acid Production, International Conference on Systems Biology
34. NissenTL
Kielland-BrandtMC
NielsenJ
VilladsenJ
2000 Optimization of Ethanol Production in Saccharomyces cerevisiae by Metabolic Engineering of the Ammonium Assimilation. Metab Eng 2 69 77
35. DrummondDA
RavalA
WilkeCO
2006 A Single Determinant Dominates the Rate of Yeast Protein Evolution. Mol Biol Evol 23 327 337
36. DrummondDA
BloomJD
AdamiC
WilkeCO
ArnoldFH
2005 Why highly expressed proteins evolve slowly. Proc Natl Acad Sci U S A 102 14338 14343
37. BojSF
PetrovD
FerrerJ
2010 Epistasis of Transcriptomes Reveals Synergism between Transcriptional Activators Hnf1α and Hnf4α. PLoS Genet 6 e1000970 doi:10.1371/journal.pgen.1000970
38. LunzerM
GoldingGB
DeanAM
2010 Pervasive Cryptic Epistasis in Molecular Evolution. PLoS Genet 6 e1001162 doi:10.1371/journal.pgen.1001162
39. RamakrishnaR
EdwardsJS
McCullochA
PalssonBO
2001 Flux-balance analysis of mitochondrial energy metabolism: consequences of systemic stoichiometric constraints. Am J Physiol Regul Integr Comp Physiol 280 R695 704
40. HolzhütterH
2004 the Principle of Flux Minimization and Its Application to Estimate Stationary Fluxes in Metabolic Networks. Eur J Biochem 271 2905 2922
41. EdwardsJS
IbarraRU
PalssonBO
2001 In silico predictions of Escherichia coli metabolic capabilities are consistent with experimental data. Nat Biotechnol 19 125 130
42. WallDP
HirshAE
FraserHB
KummJ
GiaeverG
2005 Functional genomic analysis of the rates of protein evolution. Proc Natl Acad Sci U S A 102 5483 5488
43. McKusickVA
2007 Mendelian Inheritance in Man and Its Online Version, OMIM. Am J Hum Genet 80 588 604
44. KanehisaM
GotoS
2000 KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Res 28 27 30
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2011 Číslo 2
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
Najčítanejšie v tomto čísle
- Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci
- MiRNA Control of Vegetative Phase Change in Trees
- The Cardiac Transcription Network Modulated by Gata4, Mef2a, Nkx2.5, Srf, Histone Modifications, and MicroRNAs
- Genome-Wide Transcript Profiling of Endosperm without Paternal Contribution Identifies Parent-of-Origin–Dependent Regulation of