Genome-wide Determinants of Proviral Targeting, Clonal Abundance and Expression in Natural HTLV-1 Infection
The regulation of proviral latency is a central problem in retrovirology. We postulate that the genomic integration site of human T lymphotropic virus type 1 (HTLV-1) determines the pattern of expression of the provirus, which in turn determines the abundance and pathogenic potential of infected T cell clones in vivo. We recently developed a high-throughput method for the genome-wide amplification, identification and quantification of proviral integration sites. Here, we used this protocol to test two hypotheses. First, that binding sites for transcription factors and chromatin remodelling factors in the genome flanking the proviral integration site of HTLV-1 are associated with integration targeting, spontaneous proviral expression, and in vivo clonal abundance. Second, that the transcriptional orientation of the HTLV-1 provirus relative to that of the nearest host gene determines spontaneous proviral expression and in vivo clonal abundance. Integration targeting was strongly associated with the presence of a binding site for specific host transcription factors, especially STAT1 and p53. The presence of the chromatin remodelling factors BRG1 and INI1 and certain host transcription factors either upstream or downstream of the provirus was associated respectively with silencing or spontaneous expression of the provirus. Cells expressing HTLV-1 Tax protein were significantly more frequent in clones of low abundance in vivo. We conclude that transcriptional interference and chromatin remodelling are critical determinants of proviral latency in natural HTLV-1 infection.
Vyšlo v časopise:
Genome-wide Determinants of Proviral Targeting, Clonal Abundance and Expression in Natural HTLV-1 Infection. PLoS Pathog 9(3): e32767. doi:10.1371/journal.ppat.1003271
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1003271
Souhrn
The regulation of proviral latency is a central problem in retrovirology. We postulate that the genomic integration site of human T lymphotropic virus type 1 (HTLV-1) determines the pattern of expression of the provirus, which in turn determines the abundance and pathogenic potential of infected T cell clones in vivo. We recently developed a high-throughput method for the genome-wide amplification, identification and quantification of proviral integration sites. Here, we used this protocol to test two hypotheses. First, that binding sites for transcription factors and chromatin remodelling factors in the genome flanking the proviral integration site of HTLV-1 are associated with integration targeting, spontaneous proviral expression, and in vivo clonal abundance. Second, that the transcriptional orientation of the HTLV-1 provirus relative to that of the nearest host gene determines spontaneous proviral expression and in vivo clonal abundance. Integration targeting was strongly associated with the presence of a binding site for specific host transcription factors, especially STAT1 and p53. The presence of the chromatin remodelling factors BRG1 and INI1 and certain host transcription factors either upstream or downstream of the provirus was associated respectively with silencing or spontaneous expression of the provirus. Cells expressing HTLV-1 Tax protein were significantly more frequent in clones of low abundance in vivo. We conclude that transcriptional interference and chromatin remodelling are critical determinants of proviral latency in natural HTLV-1 infection.
Zdroje
1. HanY, LinYB, AnW, XuJ, YangHC, et al. (2008) Orientation-dependent regulation of integrated HIV-1 expression by host gene transcriptional readthrough. Cell Host Microbe 4: 134–146.
2. LenasiT, ContrerasX, PeterlinBM (2008) Transcriptional interference antagonizes proviral gene expression to promote HIV latency. Cell Host Microbe 4: 123–133.
3. IgakuraT, StinchcombeJC, GoonPK, TaylorGP, WeberJN, et al. (2003) Spread of HTLV-I between lymphocytes by virus-induced polarization of the cytoskeleton. Science 299: 1713–1716.
4. BanghamCR (2009) CTL quality and the control of human retroviral infections. Eur J Immunol 39: 1700–1712.
5. IwanagaM, WatanabeT, UtsunomiyaA, OkayamaA, UchimaruK, et al. (2010) Human T-cell leukemia virus type I (HTLV-1) proviral load and disease progression in asymptomatic HTLV-1 carriers: a nationwide prospective study in Japan. Blood 116: 1211–1219.
6. MatsuzakiT, NakagawaM, NagaiM, UsukuK, HiguchiI, et al. (2001) HTLV-I proviral load correlates with progression of motor disability in HAM/TSP: analysis of 239 HAM/TSP patients including 64 patients followed up for 10 years. J Neurovirol 7: 228–234.
7. WattelE, VartanianJP, PannetierC, Wain-HobsonS (1995) Clonal expansion of human T-cell leukemia virus type I-infected cells in asymptomatic and symptomatic carriers without malignancy. J Virol 69: 2863–2868.
8. CookLB, RowanAG, MelamedA, TaylorGP, BanghamCR (2012) HTLV-1-infected T cells contain a single integrated provirus in natural infection. Blood 120: 3488–3490.
9. DerseD, CriseB, LiY, PrinclerG, LumN, et al. (2007) Human T-cell leukemia virus type 1 integration target sites in the human genome: comparison with those of other retroviruses. J Virol 81: 6731–6741.
10. MeekingsKN, LeipzigJ, BushmanFD, TaylorGP, BanghamCR (2008) HTLV-1 integration into transcriptionally active genomic regions is associated with proviral expression and with HAM/TSP. PLoS Pathog 4: e1000027.
11. GilletNA, MalaniN, MelamedA, GormleyN, CarterR, et al. (2011) The host genomic environment of the provirus determines the abundance of HTLV-1-infected T-cell clones. Blood 117: 3113–3122.
12. JacobsonS, ShidaH, McFarlinDE, FauciAS, KoenigS (1990) Circulating CD8+ cytotoxic T lymphocytes specific for HTLV-I pX in patients with HTLV-I associated neurological disease. Nature 348: 245–248.
13. ParkerCE, DaenkeS, NightingaleS, BanghamCR (1992) Activated, HTLV-1-specific cytotoxic T-lymphocytes are found in healthy seropositives as well as in patients with tropical spastic paraparesis. Virology 188: 628–636.
14. GoonPK, BiancardiA, FastN, IgakuraT, HanonE, et al. (2004) Human T cell lymphotropic virus (HTLV) type-1-specific CD8+ T cells: frequency and immunodominance hierarchy. J Infect Dis 189: 2294–2298.
15. HanonE, HallS, TaylorGP, SaitoM, DavisR, et al. (2000) Abundant tax protein expression in CD4+ T cells infected with human T-cell lymphotropic virus type I (HTLV-I) is prevented by cytotoxic T lymphocytes. Blood 95: 1386–1392.
16. SatouY, YasunagaJ, YoshidaM, MatsuokaM (2006) HTLV-I basic leucine zipper factor gene mRNA supports proliferation of adult T cell leukemia cells. Proc Natl Acad Sci U S A 103: 720–725.
17. MacnamaraA, RowanA, HilburnS, KadolskyU, FujiwaraH, et al. (2010) HLA class I binding of HBZ determines outcome in HTLV-1 infection. PLoS Pathog 6: e1001117.
18. HilburnS, RowanA, DemontisMA, MacNamaraA, AsquithB, et al. (2011) In vivo expression of human T-lymphotropic virus type 1 basic leucine-zipper protein generates specific CD8+ and CD4+ T-lymphocyte responses that correlate with clinical outcome. J Infect Dis 203: 529–536.
19. LandryS, HalinM, VargasA, LemassonI, MesnardJM, et al. (2009) Upregulation of human T-cell leukemia virus type 1 antisense transcription by the viral tax protein. J Virol 83: 2048–2054.
20. GaudrayG, GachonF, BasbousJ, Biard-PiechaczykM, DevauxC, et al. (2002) The complementary strand of the human T-cell leukemia virus type 1 RNA genome encodes a bZIP transcription factor that down-regulates viral transcription. J Virol 76: 12813–12822.
21. CiuffiA, LlanoM, PoeschlaE, HoffmannC, LeipzigJ, et al. (2005) A role for LEDGF/p75 in targeting HIV DNA integration. Nat Med 11: 1287–1289.
22. BernsteinBE, BirneyE, DunhamI, GreenED, GunterC, et al. (2012) An integrated encyclopedia of DNA elements in the human genome. Nature 489: 57–74.
23. DurandCM, BlanksonJN, SilicianoRF (2012) Developing strategies for HIV-1 eradication. Trends Immunol 33: 554–562.
24. BanghamCR, MeekingsK, ToulzaF, NejmeddineM, MajorovitsE, et al. (2009) The immune control of HTLV-1 infection: selection forces and dynamics. Front Biosci 14: 2889–2903.
25. TattermuschS, SkinnerJA, ChaussabelD, BanchereauJ, BerryMP, et al. (2012) Systems biology approaches reveal a specific interferon-inducible signature in HTLV-1 associated myelopathy. PLoS Pathog 8: e1002480.
26. SantoniFA, HartleyO, LubanJ (2010) Deciphering the code for retroviral integration target site selection. PLoS Comput Biol 6: e1001008.
27. RainJC, CribierA, GerardA, EmilianiS, BenarousR (2009) Yeast two-hybrid detection of integrase-host factor interactions. Methods 47: 291–297.
28. CherepanovP, MaertensG, ProostP, DevreeseB, Van BeeumenJ, et al. (2003) HIV-1 integrase forms stable tetramers and associates with LEDGF/p75 protein in human cells. J Biol Chem 278: 372–381.
29. MaertensG, CherepanovP, PluymersW, BusschotsK, De ClercqE, et al. (2003) LEDGF/p75 is essential for nuclear and chromosomal targeting of HIV-1 integrase in human cells. J Biol Chem 278: 33528–33539.
30. ShanL, YangHC, RabiSA, BravoHC, ShroffNS, et al. (2011) Influence of host gene transcription level and orientation on HIV-1 latency in a primary-cell model. J Virol 85: 5384–5393.
31. EuskirchenG, AuerbachRK, SnyderM (2012) SWI/SNF Chromatin-remodeling Factors: Multiscale Analyses and Diverse Functions. J Biol Chem 287: 30897–30905.
32. HoL, JothiR, RonanJL, CuiK, ZhaoK, et al. (2009) An embryonic stem cell chromatin remodeling complex, esBAF, is an essential component of the core pluripotency transcriptional network. Proc Natl Acad Sci U S A 106: 5187–5191.
33. DeS, WursterAL, PrechtP, WoodWH3rd, BeckerKG, et al. (2011) Dynamic BRG1 recruitment during T helper differentiation and activation reveals distal regulatory elements. Mol Cell Biol 31: 1512–1527.
34. EuskirchenGM, AuerbachRK, DavidovE, GianoulisTA, ZhongG, et al. (2011) Diverse roles and interactions of the SWI/SNF chromatin remodeling complex revealed using global approaches. PLoS Genet 7: e1002008.
35. EasleyR, CarpioL, GuendelI, KlaseZ, ChoiS, et al. (2010) Human T-lymphotropic virus type 1 transcription and chromatin-remodeling complexes. J Virol 84: 4755–4768.
36. RafatiH, ParraM, HakreS, MoshkinY, VerdinE, et al. (2011) Repressive LTR nucleosome positioning by the BAF complex is required for HIV latency. PLoS Biol 9: e1001206.
37. KalpanaGV, MarmonS, WangW, CrabtreeGR, GoffSP (1994) Binding and stimulation of HIV-1 integrase by a human homolog of yeast transcription factor SNF5. Science 266: 2002–2006.
38. TurelliP, DoucasV, CraigE, MangeatB, KlagesN, et al. (2001) Cytoplasmic recruitment of INI1 and PML on incoming HIV preintegration complexes: interference with early steps of viral replication. Mol Cell 7: 1245–1254.
39. MatsuokaM, JeangKT (2011) Human T-cell leukemia virus type 1 (HTLV-1) and leukemic transformation: viral infectivity, Tax, HBZ and therapy. Oncogene 30: 1379–1389.
40. MarriottSJ, SemmesOJ (2005) Impact of HTLV-I Tax on cell cycle progression and the cellular DNA damage repair response. Oncogene 24: 5986–5995.
41. AsquithB, ZhangY, MosleyAJ, de LaraCM, WallaceDL, et al. (2007) In vivo T lymphocyte dynamics in humans and the impact of human T-lymphotropic virus 1 infection. Proc Natl Acad Sci U S A 104: 8035–8040.
42. KannagiM, HaradaS, MaruyamaI, InokoH, IgarashiH, et al. (1991) Predominant recognition of human T cell leukemia virus type I (HTLV-I) pX gene products by human CD8+ cytotoxic T cells directed against HTLV-I-infected cells. Int Immunol 3: 761–767.
43. TaniguchiY, NosakaK, YasunagaJ, MaedaM, MuellerN, et al. (2005) Silencing of human T-cell leukemia virus type I gene transcription by epigenetic mechanisms. Retrovirology 2: 64.
44. KattanT, MacNamaraA, RowanAG, NoseH, MosleyAJ, et al. (2009) The avidity and lytic efficiency of the CTL response to HTLV-1. J Immunol 182: 5723–5729.
45. NejmeddineM, BarnardAL, TanakaY, TaylorGP, BanghamCR (2005) Human T-lymphotropic virus, type 1, tax protein triggers microtubule reorientation in the virological synapse. J Biol Chem 280: 29653–29660.
46. NejmeddineM, NegiVS, MukherjeeS, TanakaY, OrthK, et al. (2009) HTLV-1-Tax and ICAM-1 act on T-cell signal pathways to polarize the microtubule-organizing center at the virological synapse. Blood 114: 1016–1025.
47. NiewieskS, DaenkeS, ParkerCE, TaylorG, WeberJ, et al. (1995) Naturally occurring variants of human T-cell leukemia virus type I Tax protein impair its recognition by cytotoxic T lymphocytes and the transactivation function of Tax. J Virol 69: 2649–2653.
48. RichardsonJH, EdwardsAJ, CruickshankJK, RudgeP, DalgleishAG (1990) In vivo cellular tropism of human T-cell leukemia virus type 1. J Virol 64: 5682–5687.
49. HanonE, StinchcombeJC, SaitoM, AsquithBE, TaylorGP, et al. (2000) Fratricide among CD8(+) T lymphocytes naturally infected with human T cell lymphotropic virus type I. Immunity 13: 657–664.
50. AsquithB, MosleyAJ, HeapsA, TanakaY, TaylorGP, et al. (2005) Quantification of the virus-host interaction in human T lymphotropic virus I infection. Retrovirology 2: 75.
51. MiyoshiI, KubonishiI, SumidaM, HirakiS, TsubotaT, et al. (1980) A novel T-cell line derived from adult T-cell leukemia. Gann 71: 155–156.
52. GiardineB, RiemerC, HardisonRC, BurhansR, ElnitskiL, et al. (2005) Galaxy: a platform for interactive large-scale genome analysis. Genome Res 15: 1451–1455.
53. GoecksJ, NekrutenkoA, TaylorJ (2010) Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences. Genome Biol 11: R86.
54. BlankenbergD, Von KusterG, CoraorN, AnandaG, LazarusR, et al. (2010) Galaxy: a web-based genome analysis tool for experimentalists. Curr Protoc Mol Biol Chapter 19: Unit 19 10 11–21.
55. NagaiM, UsukuK, MatsumotoW, KodamaD, TakenouchiN, et al. (1998) Analysis of HTLV-I proviral load in 202 HAM/TSP patients and 243 asymptomatic HTLV-I carriers: high proviral load strongly predisposes to HAM/TSP. J Neurovirol 4: 586–593.
56. KarolchikD, HinrichsAS, FureyTS, RoskinKM, SugnetCW, et al. (2004) The UCSC Table Browser data retrieval tool. Nucleic Acids Res 32: D493–496.
57. JothiR, CuddapahS, BarskiA, CuiK, ZhaoK (2008) Genome-wide identification of in vivo protein-DNA binding sites from ChIP-Seq data. Nucleic Acids Res 36: 5221–5231.
Štítky
Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
PLOS Pathogens
2013 Číslo 3
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Koronavirus hýbe světem: Víte jak se chránit a jak postupovat v případě podezření?
Najčítanejšie v tomto čísle
- Escapes Fumagillin Control in Honey Bees
- TIM-3 Does Not Act as a Receptor for Galectin-9
- Influenza Virus Aerosols in Human Exhaled Breath: Particle Size, Culturability, and Effect of Surgical Masks
- Redefining the Immune System as a Social Interface for Cooperative Processes