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Integrated Genome-Scale Prediction of Detrimental Mutations in Transcription Networks


A central challenge in genetics is to understand when and why mutations alter the phenotype of an organism. The consequences of gene inhibition have been systematically studied and can be predicted reasonably well across a genome. However, many sequence variants important for disease and evolution may alter gene regulation rather than gene function. The consequences of altering a regulatory interaction (or “edge”) rather than a gene (or “node”) in a network have not been as extensively studied. Here we use an integrative analysis and evolutionary conservation to identify features that predict when the loss of a regulatory interaction is detrimental in the extensively mapped transcription network of budding yeast. Properties such as the strength of an interaction, location and context in a promoter, regulator and target gene importance, and the potential for compensation (redundancy) associate to some extent with interaction importance. Combined, however, these features predict quite well whether the loss of a regulatory interaction is detrimental across many promoters and for many different transcription factors. Thus, despite the potential for regulatory diversity, common principles can be used to understand and predict when changes in regulation are most harmful to an organism.


Vyšlo v časopise: Integrated Genome-Scale Prediction of Detrimental Mutations in Transcription Networks. PLoS Genet 7(5): e32767. doi:10.1371/journal.pgen.1002077
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002077

Souhrn

A central challenge in genetics is to understand when and why mutations alter the phenotype of an organism. The consequences of gene inhibition have been systematically studied and can be predicted reasonably well across a genome. However, many sequence variants important for disease and evolution may alter gene regulation rather than gene function. The consequences of altering a regulatory interaction (or “edge”) rather than a gene (or “node”) in a network have not been as extensively studied. Here we use an integrative analysis and evolutionary conservation to identify features that predict when the loss of a regulatory interaction is detrimental in the extensively mapped transcription network of budding yeast. Properties such as the strength of an interaction, location and context in a promoter, regulator and target gene importance, and the potential for compensation (redundancy) associate to some extent with interaction importance. Combined, however, these features predict quite well whether the loss of a regulatory interaction is detrimental across many promoters and for many different transcription factors. Thus, despite the potential for regulatory diversity, common principles can be used to understand and predict when changes in regulation are most harmful to an organism.


Zdroje

1. LeeILehnerBCrombieCWongWFraserAG 2008 A single gene network accurately predicts phenotypic effects of gene perturbation in Caenorhabditis elegans. Nat Genet 40 181 188

2. Peña-CastilloLTasanMMyersCLLeeHJoshiT 2008 A critical assessment of Mus musculus gene function prediction using integrated genomic evidence. Genome Biol 9 Suppl 1 S2

3. GagneurJSinhaHPerocchiFBourgonRHuberW 2009 Genome-wide allele- and strand-specific expression profiling. Mol Syst Biol 5 274

4. GaschAPMosesAMChiangDYFraserHBBerardiniM 2004 Conservation and evolution of cis-regulatory systems in ascomycete fungi. PLoS Biol 2 e398 doi:10.1371/journal.pbio.0020398

5. IhmelsJBergmannSGerami-NejadMYanaiIMcClellanM 2005 Rewiring of the yeast transcriptional network through the evolution of motif usage. Science 309 938 940

6. TanayARegevAShamirR 2005 Conservation and evolvability in regulatory networks: the evolution of ribosomal regulation in yeast. Proc Natl Acad Sci U S A 102 7203 7208

7. CarrollSB 2008 Evo-devo and an expanding evolutionary synthesis: a genetic theory of morphological evolution. Cell 134 25 36

8. KingMCWilsonAC 1975 Evolution at two levels in humans and chimpanzees. Science 188 107 116

9. Prud'hommeBGompelNCarrollSB 2007 Emerging principles of regulatory evolution. Proc Natl Acad Sci U S A 104 Suppl 1 8605 8612

10. HindorffLASethupathyPJunkinsHARamosEMMehtaJP 2009 Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci U S A 106 9362 9367

11. DrezeMCharloteauxBMilsteinSVidalainP-OYildirimMA 2009 ’Edgetic‚ perturbation of a C. elegans BCL2 ortholog. Nat Methods 6 843 849

12. ZhongQSimonisNLiQ-RCharloteauxBHeuzeF 2009 Edgetic perturbation models of human inherited disorders. Mol Syst Biol 5 321

13. StormoGD 2000 DNA binding sites: representation and discovery. Bioinformatics 16 16 23

14. WunderlichZMirnyLA 2009 Different gene regulation strategies revealed by analysis of binding motifs. Trends Genet 25 434 440

15. BoyerLALeeTIColeMFJohnstoneSELevineSS 2005 Core transcriptional regulatory circuitry in human embryonic stem cells. Cell 122 947 956

16. HarbisonCTGordonDBLeeTIRinaldiNJMacisaacKD 2004 Transcriptional regulatory code of a eukaryotic genome. Nature 431 99 104

17. MacArthurSLiX-YLiJBrownJBChuHC 2009 Developmental roles of 21 Drosophila transcription factors are determined by quantitative differences in binding to an overlapping set of thousands of genomic regions. Genome Biol 10 R80

18. OdomDTDowellRDJacobsenESGordonWDanfordTW 2007 Tissue-specific transcriptional regulation has diverged significantly between human and mouse. Nat Genet 39 730 732

19. OuyangZZhouQWongWH 2009 ChIP-Seq of transcription factors predicts absolute and differential gene expression in embryonic stem cells. Proc Natl Acad Sci U S A 106 21521 21526

20. SchmidtDWilsonMDBallesterBSchwaliePCBrownGD Five-Vertebrate ChIP-seq Reveals the Evolutionary Dynamics of Transcription Factor Binding. Science

21. yong LiXMacArthurSBourgonRNixDPollardDA 2008 Transcription factors bind thousands of active and inactive regions in the Drosophila blastoderm. PLoS Biol 6 e27 doi:10.1371/journal.pbio.0060027

22. MosesAMChiangDYKellisMLanderESEisenMB 2003 Position specific variation in the rate of evolution in transcription factor binding sites. BMC Evol Biol 3 19

23. ChenKvan NimwegenERajewskyNSiegalML Correlating gene expression variation with cis-regulatory polymorphism in Saccharomyces cerevisiae. Genome Biol Evol

24. DonigerSWKimHSSwainDCorcueraDWilliamsM 2008 A catalog of neutral and deleterious polymorphism in yeast. PLoS Genet 4 e1000183 doi:10.1371/journal.pgen.1000183

25. TiroshIWeinbergerABezalelDKaganovichMBarkaiN 2008 On the relation between promoter divergence and gene expression evolution. Mol Syst Biol 4 159

26. BiluYBarkaiN 2005 The design of transcription-factor binding sites is affected by combinatorial regulation. Genome Biol 6 R103

27. JohnsonRSamuelJNgCKLJauchRStantonLW 2009 Evolution of the vertebrate gene regulatory network controlled by the transcriptional repressor REST. Mol Biol Evol 26 1491 1507

28. KimJHeXSinhaS 2009 Evolution of regulatory sequences in 12 Drosophila species. PLoS Genet 5 e1000330 doi:10.1371/journal.pgen.1000330

29. MustonenVKinneyJCallanCGLässigM 2008 Energy-dependent fitness: a quantitative model for the evolution of yeast transcription factor binding sites. Proc Natl Acad Sci U S A 105 12376 12381

30. TiroshIBarkaiN 2008 Two strategies for gene regulation by promoter nucleosomes. Genome Res 18 1084 1091

31. MacIsaacKDWangTGordonDBGiffordDKStormoGD 2006 An improved map of conserved regulatory sites for Saccharomyces cerevisiae. BMC Bioinformatics 7 113

32. McDonaldJHKreitmanM 1991 Adaptive protein evolution at the Adh locus in Drosophila. Nature 351 652 654

33. LitiGCarterDMMosesAMWarringerJPartsL 2009 Population genomics of domestic and wild yeasts. Nature 458 337 341

34. GiaeverGChuAMNiLConnellyCRilesL 2002 Functional profiling of the Saccharomyces cerevisiae genome. Nature 418 387 391

35. GelperinDMWhiteMAWilkinsonMLKonYKungLA 2005 Biochemical and genetic analysis of the yeast proteome with a movable ORF collection. Genes Dev 19 2816 2826

36. SopkoRHuangDPrestonNChuaGPappBz 2006 Mapping pathways and phenotypes by systematic gene overexpression. Mol Cell 21 319 330

37. VavouriTSempleJIGarcia-VerdugoRLehnerB 2009 Intrinsic protein disorder and interaction promiscuity are widely associated with dosage sensitivity. Cell 138 198 208

38. FieldYKaplanNFondufe-MittendorfYMooreIKSharonE 2008 Distinct modes of regulation by chromatin encoded through nucleosome positioning signals. PLoS Comput Biol 4 e1000216 doi:10.1371/journal.pcbi.1000216

39. GerkeJLorenzKCohenB 2009 Genetic interactions between transcription factors cause natural variation in yeast. Science 323 498 501

40. OhnoS 1970 Evolution by gene duplication. New York Springer Verlag

41. VavouriTSempleJILehnerB 2008 Widespread conservation of genetic redundancy during a billion years of eukaryotic evolution. Trends Genet 24 485 488

42. GertzJSiggiaEDCohenBA 2009 Analysis of combinatorial cis-regulation in synthetic and genomic promoters. Nature 457 215 218

43. GiorgettiLSiggersTTianaGCaprara GNotarbartolo S Noncooperative interactions between transcription factors and clustered DNA binding sites enable graded transcriptional responses to environmental inputs. Mol Cell 37 418 428

44. ZeiserSLiebscherHVTiedemannHRubio-AliagaIPrzemeckGKH 2006 Number of active transcription factor binding sites is essential for the Hes7 oscillator. Theor Biol Med Model 3 11

45. ZhengJBenschopJJShalesMKemmerenP GreenblattJ Epistatic relationships reveal the functional organization of yeast transcription factors. Mol Syst Biol 6 420

46. KellisMPattersonNEndrizziMBirrenBLanderES 2003 Sequencing and comparison of yeast species to identify genes and regulatory elements. Nature 423 241 254

47. BrownCAMurrayAWVerstrepenKJ 2010 Rapid expansion and functional divergence of subtelomeric gene families in yeasts. Curr Biol 20 895 903

48. TeytelmanLEisenMBRineJ 2008 Silent but not static: accelerated base-pair substitution in silenced chromatin of budding yeasts. PLoS Genet 4 e1000247 doi:10.1371/journal.pgen.1000247

49. BatadaNNHurstLD 2007 Evolution of chromosome organization driven by selection for reduced gene expression noise. Nat Genet 39 945 949

50. MakHCPillusLIdekerT 2009 Dynamic reprogramming of transcription factors to and from the subtelomere. Genome Res 19 1014 1025

51. LiebJDLiuXBotsteinDBrownPO 2001 Promoter-specific binding of Rap1 revealed by genome-wide maps of protein-DNA association. Nat Genet 28 327 334

52. MarcandSBuckSWMorettiPGilsonEShoreD 1996 Silencing of genes at nontelomeric sites in yeast is controlled by sequestration of silencing factors at telomeres by Rap 1 protein. Genes Dev 10 1297 1309

53. JothiRBalajiSWusterAGrochowJAGsponerJr 2009 Genomic analysis reveals a tight link between transcription factor dynamics and regulatory network architecture. Mol Syst Biol 5 294

54. SegalEShapiraMRegevAPe'erDBotsteinD 2003 Module networks: identifying regulatory modules and their condition-specific regulators from gene expression data. Nat Genet 34 166 176

55. ChinC-SChuangJHLiH 2005 Genome-wide regulatory complexity in yeast promoters: separation of functionally conserved and neutral sequence. Genome Res 15 205 213

56. ZhuCByersKJRPMcCordRPShiZBergerMF 2009 High-resolution DNA-binding specificity analysis of yeast transcription factors. Genome Res 19 556 566

57. ChanCSElementoOTavazoieS 2005 Revealing posttranscriptional regulatory elements through network-level conservation. PLoS Comput Biol 1 e69 doi:10.1371/journal.pcbi.0010069

58. DermitzakisETClarkAG 2002 Evolution of transcription factor binding sites in Mammalian gene regulatory regions: conservation and turnover. Mol Biol Evol 19 1114 1121

59. DonigerSWFayJC 2007 Frequent gain and loss of functional transcription factor binding sites. PLoS Comput Biol 3 e99 doi:10.1371/journal.pcbi.0030099

60. NagalakshmiUWangZWaernKShouCRahaD 2008 The transcriptional landscape of the yeast genome defined by RNA sequencing. Science 320 1344 1349

61. SempleJIVavouriTLehnerB 2008 A simple principle concerning the robustness of protein complex activity to changes in gene expression. BMC Syst Biol 2 1

62. ZhuJZhangMQ 1999 SCPD: a promoter database of the yeast Saccharomyces cerevisiae. Bioinformatics 15 607 611

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Genetika Reprodukčná medicína

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PLOS Genetics


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