#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

HIF- and Non-HIF-Regulated Hypoxic Responses Require the Estrogen-Related Receptor in


Low-oxygen tolerance is supported by an adaptive response that includes a coordinate shift in metabolism and the activation of a transcriptional program that is driven by the hypoxia-inducible factor (HIF) pathway. The precise contribution of HIF-1a in the adaptive response, however, has not been determined. Here, we investigate how HIF influences hypoxic adaptation throughout Drosophila melanogaster development. We find that hypoxic-induced transcriptional changes are comprised of HIF-dependent and HIF-independent pathways that are distinct and separable. We show that normoxic set-points of carbohydrate metabolites are significantly altered in sima mutants and that these animals are unable to mobilize glycogen in hypoxia. Furthermore, we find that the estrogen-related receptor (dERR), which is a global regulator of aerobic glycolysis in larvae, is required for a competent hypoxic response. dERR binds to dHIFa and participates in the HIF-dependent transcriptional program in hypoxia. In addition, dERR acts in the absence of dHIFa in hypoxia and a significant portion of HIF-independent transcriptional responses can be attributed to dERR actions, including upregulation of glycolytic transcripts. These results indicate that competent hypoxic responses arise from complex interactions between HIF-dependent and -independent mechanisms, and that dERR plays a central role in both of these programs.


Vyšlo v časopise: HIF- and Non-HIF-Regulated Hypoxic Responses Require the Estrogen-Related Receptor in. PLoS Genet 9(1): e32767. doi:10.1371/journal.pgen.1003230
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003230

Souhrn

Low-oxygen tolerance is supported by an adaptive response that includes a coordinate shift in metabolism and the activation of a transcriptional program that is driven by the hypoxia-inducible factor (HIF) pathway. The precise contribution of HIF-1a in the adaptive response, however, has not been determined. Here, we investigate how HIF influences hypoxic adaptation throughout Drosophila melanogaster development. We find that hypoxic-induced transcriptional changes are comprised of HIF-dependent and HIF-independent pathways that are distinct and separable. We show that normoxic set-points of carbohydrate metabolites are significantly altered in sima mutants and that these animals are unable to mobilize glycogen in hypoxia. Furthermore, we find that the estrogen-related receptor (dERR), which is a global regulator of aerobic glycolysis in larvae, is required for a competent hypoxic response. dERR binds to dHIFa and participates in the HIF-dependent transcriptional program in hypoxia. In addition, dERR acts in the absence of dHIFa in hypoxia and a significant portion of HIF-independent transcriptional responses can be attributed to dERR actions, including upregulation of glycolytic transcripts. These results indicate that competent hypoxic responses arise from complex interactions between HIF-dependent and -independent mechanisms, and that dERR plays a central role in both of these programs.


Zdroje

1. SemenzaGL (2011) Oxygen sensing, homeostasis, and disease. N Engl J Med 365: 537–547.

2. MurdochC, MuthanaM, LewisCE (2005) Hypoxia regulates macrophage functions in inflammation. J Immunol 175: 6257–6263.

3. FineLG, NormanJT (2008) Chronic hypoxia as a mechanism of progression of chronic kidney diseases: from hypothesis to novel therapeutics. Kidney Int 74: 867–872.

4. SemenzaGL (2003) Targeting HIF-1 for cancer therapy. Nat Rev Cancer 3: 721–732.

5. BruickRK, McKnightSL (2001) A conserved family of prolyl-4-hydroxylases that modify HIF. Science 294: 1337–1340.

6. EpsteinAC, GleadleJM, McNeillLA, HewitsonKS, O'RourkeJ, et al. (2001) C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. Cell 107: 43–54.

7. YuF, WhiteSB, ZhaoQ, LeeFS (2001) HIF-1alpha binding to VHL is regulated by stimulus-sensitive proline hydroxylation. Proc Natl Acad Sci U S A 98: 9630–9635.

8. IvanM, KondoK, YangH, KimW, ValiandoJ, et al. (2001) HIFalpha targeted for VHL-mediated destruction by proline hydroxylation: implications for O2 sensing. Science 292: 464–468.

9. JaakkolaP, MoleDR, TianYM, WilsonMI, GielbertJ, et al. (2001) Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation. Science 292: 468–472.

10. KamuraT, SatoS, IwaiK, Czyzyk-KrzeskaM, ConawayRC, et al. (2000) Activation of HIF1alpha ubiquitination by a reconstituted von Hippel-Lindau (VHL) tumor suppressor complex. Proc Natl Acad Sci U S A 97: 10430–10435.

11. BellEL, KlimovaTA, EisenbartJ, MoraesCT, MurphyMP, et al. (2007) The Qo site of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production. J Cell Biol 177: 1029–1036.

12. KlimovaT, ChandelNS (2008) Mitochondrial complex III regulates hypoxic activation of HIF. Cell Death Differ 15: 660–666.

13. CarmelietP, DorY, HerbertJM, FukumuraD, BrusselmansK, et al. (1998) Role of HIF-1alpha in hypoxia-mediated apoptosis, cell proliferation and tumour angiogenesis. Nature 394: 485–490.

14. RyanHE, LoJ, JohnsonRS (1998) HIF-1 alpha is required for solid tumor formation and embryonic vascularization. Embo J 17: 3005–3015.

15. YuAY, ShimodaLA, IyerNV, HusoDL, SunX, et al. (1999) Impaired physiological responses to chronic hypoxia in mice partially deficient for hypoxia-inducible factor 1alpha. J Clin Invest 103: 691–696.

16. IyerNV, KotchLE, AganiF, LeungSW, LaughnerE, et al. (1998) Cellular and developmental control of O2 homeostasis by hypoxia-inducible factor 1 alpha. Genes Dev 12: 149–162.

17. SeagrovesTN, RyanHE, LuH, WoutersBG, KnappM, et al. (2001) Transcription factor HIF-1 is a necessary mediator of the pasteur effect in mammalian cells. Mol Cell Biol 21: 3436–3444.

18. ShenC, NettletonD, JiangM, KimSK, Powell-CoffmanJA (2005) Roles of the HIF-1 hypoxia-inducible factor during hypoxia response in Caenorhabditis elegans. J Biol Chem 280: 20580–20588.

19. MizukamiY, LiJ, ZhangX, ZimmerMA, IliopoulosO, et al. (2004) Hypoxia-inducible factor-1-independent regulation of vascular endothelial growth factor by hypoxia in colon cancer. Cancer Res 64: 1765–1772.

20. ElvidgeGP, GlennyL, AppelhoffRJ, RatcliffePJ, RagoussisJ, et al. (2006) Concordant regulation of gene expression by hypoxia and 2-oxoglutarate-dependent dioxygenase inhibition: the role of HIF-1alpha, HIF-2alpha, and other pathways. J Biol Chem 281: 15215–15226.

21. WoodSM, WiesenerMS, YeatesKM, OkadaN, PughCW, et al. (1998) Selection and analysis of a mutant cell line defective in the hypoxia-inducible factor-1 alpha-subunit (HIF-1alpha). Characterization of hif-1alpha-dependent and -independent hypoxia-inducible gene expression. J Biol Chem 273: 8360–8368.

22. WingroveJA, O'FarrellPH (1999) Nitric oxide contributes to behavioral, cellular, and developmental responses to low oxygen in Drosophila. Cell 98: 105–114.

23. HaddadGG, WymanRJ, MohseninA, SunY, KrishnanSN (1997) Behavioral and Electrophysiologic Responses of Drosophila melanogaster to Prolonged Periods of Anoxia. J Insect Physiol 43: 203–210.

24. RomeroNM, DekantyA, WappnerP (2007) Cellular and developmental adaptations to hypoxia: a Drosophila perspective. Methods Enzymol 435: 123–144.

25. BaconNC, WappnerP, O'RourkeJF, BartlettSM, ShiloB, et al. (1998) Regulation of the Drosophila bHLH-PAS protein Sima by hypoxia: functional evidence for homology with mammalian HIF-1 alpha. Biochem Biophys Res Commun 249: 811–816.

26. LiuG, RoyJ, JohnsonEA (2006) Identification and function of hypoxia-response genes in Drosophila melanogaster. Physiol Genomics 25: 134–141.

27. ZhouD, XueJ, LaiJC, SchorkNJ, WhiteKP, et al. (2008) Mechanisms underlying hypoxia tolerance in Drosophila melanogaster: hairy as a metabolic switch. PLoS Genet 4: e1000221 doi:10.1371/journal.pgen.1000221.

28. CentaninL, DekantyA, RomeroN, IrisarriM, GorrTA, et al. (2008) Cell autonomy of HIF effects in Drosophila: tracheal cells sense hypoxia and induce terminal branch sprouting. Dev Cell 14: 547–558.

29. MortimerNT, MobergKH (2009) Regulation of Drosophila embryonic tracheogenesis by dVHL and hypoxia. Dev Biol 329: 294–305.

30. MetzgerRJ, KrasnowMA (1999) Genetic control of branching morphogenesis. Science 284: 1635–1639.

31. FealaJD, CoquinL, McCullochAD, PaternostroG (2007) Flexibility in energy metabolism supports hypoxia tolerance in Drosophila flight muscle: metabolomic and computational systems analysis. Mol Syst Biol 3: 99.

32. TennessenJM, BakerKD, LamG, EvansJ, ThummelCS (2011) The Drosophila estrogen-related receptor directs a metabolic switch that supports developmental growth. Cell Metab 13: 139–148.

33. SuzukiT, MikiY, MoriyaT, ShimadaN, IshidaT, et al. (2004) Estrogen-related receptor alpha in human breast carcinoma as a potent prognostic factor. Cancer Res 64: 4670–4676.

34. SteinRA, McDonnellDP (2006) Estrogen-related receptor alpha as a therapeutic target in cancer. Endocr Relat Cancer 13 Suppl 1: S25–32.

35. SteinRA, GaillardS, McDonnellDP (2009) Estrogen-related receptor alpha induces the expression of vascular endothelial growth factor in breast cancer cells. J Steroid Biochem Mol Biol 114: 106–112.

36. AriaziEA, KrausRJ, FarrellML, JordanVC, MertzJE (2007) Estrogen-related receptor alpha1 transcriptional activities are regulated in part via the ErbB2/HER2 signaling pathway. Mol Cancer Res 5: 71–85.

37. LuD, KiriyamaY, LeeKY, GiguereV (2001) Transcriptional regulation of the estrogen-inducible pS2 breast cancer marker gene by the ERR family of orphan nuclear receptors. Cancer Res 61: 6755–6761.

38. CaiQ, LinT, KamarajugaddaS, LuJ (2012) Regulation of glycolysis and the Warburg effect by estrogen-related receptors. Oncogene

39. AoA, WangH, KamarajugaddaS, LuJ (2008) Involvement of estrogen-related receptors in transcriptional response to hypoxia and growth of solid tumors. Proc Natl Acad Sci U S A 105: 7821–7826.

40. RobinED, MurphyBJ, TheodoreJ (1984) Coordinate regulation of glycolysis by hypoxia in mammalian cells. J Cell Physiol 118: 287–290.

41. AcevedoJM, CentaninL, DekantyA, WappnerP (2010) Oxygen sensing in Drosophila: multiple isoforms of the prolyl hydroxylase fatiga have different capacity to regulate HIFalpha/Sima. PLoS ONE 5: e12390 doi:10.1371/journal.pone.0012390.

42. Lavista-LlanosS, CentaninL, IrisarriM, RussoDM, GleadleJM, et al. (2002) Control of the hypoxic response in Drosophila melanogaster by the basic helix-loop-helix PAS protein similar. Mol Cell Biol 22: 6842–6853.

43. CentaninL, RatcliffePJ, WappnerP (2005) Reversion of lethality and growth defects in Fatiga oxygen-sensor mutant flies by loss of hypoxia-inducible factor-alpha/Sima. EMBO Rep 6: 1070–1075.

44. BeissbarthT, SpeedTP (2004) GOstat: find statistically overrepresented Gene Ontologies within a group of genes. Bioinformatics 20: 1464–1465.

45. ZhangH, Bosch-MarceM, ShimodaLA, TanYS, BaekJH, et al. (2008) Mitochondrial autophagy is an HIF-1-dependent adaptive metabolic response to hypoxia. J Biol Chem 283: 10892–10903.

46. RosenfeldMG, LunyakVV, GlassCK (2006) Sensors and signals: a coactivator/corepressor/epigenetic code for integrating signal-dependent programs of transcriptional response. Genes Dev 20: 1405–1428.

47. VengellurA, WoodsBG, RyanHE, JohnsonRS, LaPresJJ (2003) Gene expression profiling of the hypoxia signaling pathway in hypoxia-inducible factor 1alpha null mouse embryonic fibroblasts. Gene Expr 11: 181–197.

48. KrishnamacharyB, Berg-DixonS, KellyB, AganiF, FeldserD, et al. (2003) Regulation of colon carcinoma cell invasion by hypoxia-inducible factor 1. Cancer Res 63: 1138–1143.

49. FirthJD, EbertBL, RatcliffePJ (1995) Hypoxic regulation of lactate dehydrogenase A. Interaction between hypoxia-inducible factor 1 and cAMP response elements. J Biol Chem 270: 21021–21027.

50. KanekoK, FuruyamaK, AburataniH, ShibaharaS (2009) Hypoxia induces erythroid-specific 5-aminolevulinate synthase expression in human erythroid cells through transforming growth factor-beta signaling. FEBS J 276: 1370–1382.

51. SuzukiA, KusakaiG, ShimojoY, ChenJ, OguraT, et al. (2005) Involvement of transforming growth factor-beta 1 signaling in hypoxia-induced tolerance to glucose starvation. J Biol Chem 280: 31557–31563.

52. ZhangFL, ShenGM, LiuXL, WangF, ZhaoHL, et al. (2011) Hypoxic induction of human erythroid-specific delta-aminolevulinate synthase mediated by hypoxia-inducible factor 1. Biochemistry 50: 1194–1202.

53. ChurchRB, RobertsonFW (1966) Biochemical analysis of genetic differences in the growth of Drosophila. Genet Res 7: 383–407.

54. GreganovaE, AltmannM, ButikoferP (2011) Unique modifications of translation elongation factors. FEBS J 278: 2613–2624.

55. OrtizPA, UlloqueR, KiharaGK, ZhengH, KinzyTG (2006) Translation elongation factor 2 anticodon mimicry domain mutants affect fidelity and diphtheria toxin resistance. J Biol Chem 281: 32639–32648.

56. GuptaPK, LiuS, BataviaMP, LepplaSH (2008) The diphthamide modification on elongation factor-2 renders mammalian cells resistant to ricin. Cell Microbiol 10: 1687–1694.

57. UniackeJ, HoltermanCE, LachanceG, FranovicA, JacobMD, et al. An oxygen-regulated switch in the protein synthesis machinery. Nature 486: 126–129.

58. DekantyA, Lavista-LlanosS, IrisarriM, OldhamS, WappnerP (2005) The insulin-PI3K/TOR pathway induces a HIF-dependent transcriptional response in Drosophila by promoting nuclear localization of HIF-alpha/Sima. J Cell Sci 118: 5431–5441.

59. BroughtonSJ, PiperMD, IkeyaT, BassTM, JacobsonJ, et al. (2005) Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands. Proc Natl Acad Sci U S A 102: 3105–3110.

60. RulifsonEJ, KimSK, NusseR (2002) Ablation of insulin-producing neurons in flies: growth and diabetic phenotypes. Science 296: 1118–1120.

61. BelgacemYH, MartinJR (2006) Disruption of insulin pathways alters trehalose level and abolishes sexual dimorphism in locomotor activity in Drosophila. J Neurobiol 66: 19–32.

62. IrizarryRA, BolstadBM, CollinF, CopeLM, HobbsB, et al. (2003) Summaries of Affymetrix GeneChip probe level data. Nucleic Acids Res 31: e15.

63. TusherVG, TibshiraniR, ChuG (2001) Significance analysis of microarrays applied to the ionizing radiation response. Proc Natl Acad Sci U S A 98: 5116–5121.

64. PalankerL, TennessenJM, LamG, ThummelCS (2009) Drosophila HNF4 regulates lipid mobilization and beta-oxidation. Cell Metab 9: 228–239.

65. MonserrateJP, ChenMY, BrachmannCB (2012) Drosophila larvae lacking the bcl-2 gene, buffy, are sensitive to nutrient stress, maintain increased basal target of rapamycin (Tor) signaling and exhibit characteristics of altered basal energy metabolism. BMC Biol 10: 63.

66. DehavenCD, EvansAM, DaiH, LawtonKA (2010) Organization of GC/MS and LC/MS metabolomics data into chemical libraries. J Cheminform 2: 9.

67. EvansAM, DeHavenCD, BarrettT, MitchellM, MilgramE (2009) Integrated, nontargeted ultrahigh performance liquid chromatography/electrospray ionization tandem mass spectrometry platform for the identification and relative quantification of the small-molecule complement of biological systems. Anal Chem 81: 6656–6667.

68. BakerKD, BecksteadRB, MangelsdorfDJ, ThummelCS (2007) Functional interactions between the Moses corepressor and DHR78 nuclear receptor regulate growth in Drosophila. Genes Dev 21: 450–464.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 1
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#