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Polyadenylation-Dependent Control of Long Noncoding RNA Expression by the Poly(A)-Binding Protein Nuclear 1


The poly(A)-binding protein nuclear 1 (PABPN1) is a ubiquitously expressed protein that is thought to function during mRNA poly(A) tail synthesis in the nucleus. Despite the predicted role of PABPN1 in mRNA polyadenylation, little is known about the impact of PABPN1 deficiency on human gene expression. Specifically, it remains unclear whether PABPN1 is required for general mRNA expression or for the regulation of specific transcripts. Using RNA sequencing (RNA–seq), we show here that the large majority of protein-coding genes express normal levels of mRNA in PABPN1–deficient cells, arguing that PABPN1 may not be required for the bulk of mRNA expression. Unexpectedly, and contrary to the view that PABPN1 functions exclusively at protein-coding genes, we identified a class of PABPN1–sensitive long noncoding RNAs (lncRNAs), the majority of which accumulated in conditions of PABPN1 deficiency. Using the spliced transcript produced from a snoRNA host gene as a model lncRNA, we show that PABPN1 promotes lncRNA turnover via a polyadenylation-dependent mechanism. PABPN1–sensitive lncRNAs are targeted by the exosome and the RNA helicase MTR4/SKIV2L2; yet, the polyadenylation activity of TRF4-2, a putative human TRAMP subunit, appears to be dispensable for PABPN1–dependent regulation. In addition to identifying a novel function for PABPN1 in lncRNA turnover, our results provide new insights into the post-transcriptional regulation of human lncRNAs.


Vyšlo v časopise: Polyadenylation-Dependent Control of Long Noncoding RNA Expression by the Poly(A)-Binding Protein Nuclear 1. PLoS Genet 8(11): e32767. doi:10.1371/journal.pgen.1003078
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003078

Souhrn

The poly(A)-binding protein nuclear 1 (PABPN1) is a ubiquitously expressed protein that is thought to function during mRNA poly(A) tail synthesis in the nucleus. Despite the predicted role of PABPN1 in mRNA polyadenylation, little is known about the impact of PABPN1 deficiency on human gene expression. Specifically, it remains unclear whether PABPN1 is required for general mRNA expression or for the regulation of specific transcripts. Using RNA sequencing (RNA–seq), we show here that the large majority of protein-coding genes express normal levels of mRNA in PABPN1–deficient cells, arguing that PABPN1 may not be required for the bulk of mRNA expression. Unexpectedly, and contrary to the view that PABPN1 functions exclusively at protein-coding genes, we identified a class of PABPN1–sensitive long noncoding RNAs (lncRNAs), the majority of which accumulated in conditions of PABPN1 deficiency. Using the spliced transcript produced from a snoRNA host gene as a model lncRNA, we show that PABPN1 promotes lncRNA turnover via a polyadenylation-dependent mechanism. PABPN1–sensitive lncRNAs are targeted by the exosome and the RNA helicase MTR4/SKIV2L2; yet, the polyadenylation activity of TRF4-2, a putative human TRAMP subunit, appears to be dispensable for PABPN1–dependent regulation. In addition to identifying a novel function for PABPN1 in lncRNA turnover, our results provide new insights into the post-transcriptional regulation of human lncRNAs.


Zdroje

1. WahleE (1991) A novel poly(A)-binding protein acts as a specificity factor in the second phase of messenger RNA polyadenylation. Cell 66: 759–768.

2. KuhnU, NemethA, MeyerS, WahleE (2003) The RNA binding domains of the nuclear poly(A)-binding protein. J Biol Chem 278: 16916–16925.

3. KerwitzY, KuhnU, LilieH, KnothA, ScheuermannT, et al. (2003) Stimulation of poly(A) polymerase through a direct interaction with the nuclear poly(A) binding protein allosterically regulated by RNA. Embo J 22: 3705–3714.

4. KuhnU, GundelM, KnothA, KerwitzY, RudelS, et al. (2009) Poly(A) tail length is controlled by the nuclear poly(A)-binding protein regulating the interaction between poly(A) polymerase and the cleavage and polyadenylation specificity factor. J Biol Chem 284: 22803–22814.

5. KuhnU, WahleE (2004) Structure and function of poly(A) binding proteins. Biochim Biophys Acta 1678: 67–84.

6. ApponiLH, LeungSW, WilliamsKR, ValentiniSR, CorbettAH, et al. (2010) Loss of nuclear poly(A)-binding protein 1 causes defects in myogenesis and mRNA biogenesis. Hum Mol Genet 19: 1058–1065.

7. BenoitB, MitouG, ChartierA, TemmeC, ZaessingerS, et al. (2005) An essential cytoplasmic function for the nuclear poly(A) binding protein, PABP2, in poly(A) tail length control and early development in Drosophila. Dev Cell 9: 511–522.

8. LemayJF, D'AmoursA, LemieuxC, LacknerDH, St-SauverVG, et al. (2010) The nuclear poly(A)-binding protein interacts with the exosome to promote synthesis of noncoding small nucleolar RNAs. Mol Cell 37: 34–45.

9. HurschlerBA, HarrisDT, GrosshansH (2011) The type II poly(A)-binding protein PABP-2 genetically interacts with the let-7 miRNA and elicits heterochronic phenotypes in Caenorhabditis elegans. Nucleic Acids Res 39: 5647–5657.

10. BraisB (2009) Oculopharyngeal muscular dystrophy: a polyalanine myopathy. Curr Neurol Neurosci Rep 9: 76–82.

11. BouchardJP, BraisB, BrunetD, GouldPV, RouleauGA (1997) Recent studies on oculopharyngeal muscular dystrophy in Quebec. Neuromuscul Disord 7 Suppl 1: S22–29.

12. BlumenSC, NisipeanuP, SadehM, AsherovA, BlumenN, et al. (1997) Epidemiology and inheritance of oculopharyngeal muscular dystrophy in Israel. Neuromuscul Disord 7 Suppl 1: S38–40.

13. BecherMW, MorrisonL, DavisLE, MakiWC, KingMK, et al. (2001) Oculopharyngeal muscular dystrophy in Hispanic New Mexicans. Jama 286: 2437–2440.

14. BraisB, BouchardJP, XieYG, RochefortDL, ChretienN, et al. (1998) Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nat Genet 18: 164–167.

15. CaladoA, TomeFM, BraisB, RouleauGA, KuhnU, et al. (2000) Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA. Hum Mol Genet 9: 2321–2328.

16. JenalM, ElkonR, Loayza-PuchF, van HaaftenG, KuhnU, et al. (2012) The Poly(A)-Binding Protein Nuclear 1 Suppresses Alternative Cleavage and Polyadenylation Sites. Cell 149: 538–553.

17. ChenHM, FutcherB, LeatherwoodJ (2011) The fission yeast RNA binding protein Mmi1 regulates meiotic genes by controlling intron specific splicing and polyadenylation coupled RNA turnover. PLoS ONE 6: e26804 doi:10.1371/journal.pone.0026804.

18. St-AndreO, LemieuxC, PerreaultA, LacknerDH, BahlerJ, et al. (2010) Negative regulation of meiotic gene expression by the nuclear poly(a)-binding protein in fission yeast. J Biol Chem 285: 27859–27868.

19. YamanakaS, YamashitaA, HarigayaY, IwataR, YamamotoM (2010) Importance of polyadenylation in the selective elimination of meiotic mRNAs in growing S. pombe cells. Embo J 29: 2173–2181.

20. LemieuxC, MargueratS, LafontaineJ, BarbezierN, BahlerJ, et al. (2011) A Pre-mRNA degradation pathway that selectively targets intron-containing genes requires the nuclear poly(A)-binding protein. Mol Cell 44: 108–119.

21. Lykke-AndersenS, BrodersenDE, JensenTH (2009) Origins and activities of the eukaryotic exosome. J Cell Sci 122: 1487–1494.

22. Lykke-AndersenS, TomeckiR, JensenTH, DziembowskiA (2011) The eukaryotic RNA exosome: same scaffold but variable catalytic subunits. RNA Biol 8: 61–66.

23. TrapnellC, PachterL, SalzbergSL (2009) TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25: 1105–1111.

24. MortazaviA, WilliamsBA, McCueK, SchaefferL, WoldB (2008) Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Methods 5: 621–628.

25. WangKC, ChangHY (2011) Molecular mechanisms of long noncoding RNAs. Mol Cell 43: 904–914.

26. CabiliMN, TrapnellC, GoffL, KoziolM, Tazon-VegaB, et al. (2011) Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev 25: 1915–1927.

27. HutchinsonJN, EnsmingerAW, ClemsonCM, LynchCR, LawrenceJB, et al. (2007) A screen for nuclear transcripts identifies two linked noncoding RNAs associated with SC35 splicing domains. BMC Genomics 8: 39.

28. BaerM, NilsenTW, CostiganC, AltmanS (1990) Structure and transcription of a human gene for H1 RNA, the RNA component of human RNase P. Nucleic Acids Res 18: 97–103.

29. MartignettiJA, BrosiusJ (1993) BC200 RNA: a neural RNA polymerase III product encoded by a monomeric Alu element. Proc Natl Acad Sci U S A 90: 11563–11567.

30. YoungTL, MatsudaT, CepkoCL (2005) The noncoding RNA taurine upregulated gene 1 is required for differentiation of the murine retina. Curr Biol 15: 501–512.

31. DieciG, PretiM, MontaniniB (2009) Eukaryotic snoRNAs: a paradigm for gene expression flexibility. Genomics 94: 83–88.

32. MorrisDP, MichelottiGA, SchwinnDA (2005) Evidence that phosphorylation of the RNA polymerase II carboxyl-terminal repeats is similar in yeast and humans. J Biol Chem 280: 31368–31377.

33. SwinburneIA, MeyerCA, LiuXS, SilverPA, BrodskyAS (2006) Genomic localization of RNA binding proteins reveals links between pre-mRNA processing and transcription. Genome Res 16: 912–921.

34. MaaleG, SteinG, MansR (1975) Effects of cordycepin and cordycepintriphosphate on polyadenylic and ribonucleic acid-synthesising enzymes from eukaryotes. Nature 255: 80–82.

35. IoannidisP, CourtisN, HavredakiM, MichailakisE, TsiapalisCM, et al. (1999) The polyadenylation inhibitor cordycepin (3′dA) causes a decline in c-MYC mRNA levels without affecting c-MYC protein levels. Oncogene 18: 117–125.

36. BirdG, FongN, GatlinJC, FarabaughS, BentleyDL (2005) Ribozyme cleavage reveals connections between mRNA release from the site of transcription and pre-mRNA processing. Mol Cell 20: 747–758.

37. TycowskiKT, ShuMD, SteitzJA (1996) A mammalian gene with introns instead of exons generating stable RNA products. Nature 379: 464–466.

38. SmithCM, SteitzJA (1998) Classification of gas5 as a multi-small-nucleolar-RNA (snoRNA) host gene and a member of the 5′-terminal oligopyrimidine gene family reveals common features of snoRNA host genes. Mol Cell Biol 18: 6897–6909.

39. PrekerP, NielsenJ, KammlerS, Lykke-AndersenS, ChristensenMS, et al. (2008) RNA exosome depletion reveals transcription upstream of active human promoters. Science 322: 1851–1854.

40. TomeckiR, KristiansenMS, Lykke-AndersenS, ChlebowskiA, LarsenKM, et al. (2010) The human core exosome interacts with differentially localized processive RNases: hDIS3 and hDIS3L. Embo J 29: 2342–2357.

41. ButlerJS, MitchellP (2010) Rrp6, Rrp47 and cofactors of the nuclear exosome. Adv Exp Med Biol 702: 91–104.

42. LubasM, ChristensenMS, KristiansenMS, DomanskiM, FalkenbyLG, et al. (2011) Interaction profiling identifies the human nuclear exosome targeting complex. Mol Cell 43: 624–637.

43. ShcherbikN, WangM, LapikYR, SrivastavaL, PestovDG (2010) Polyadenylation and degradation of incomplete RNA polymerase I transcripts in mammalian cells. EMBO Rep 11: 106–111.

44. EckmannCR, RammeltC, WahleE (2011) Control of poly(A) tail length. Wiley Interdiscip Rev RNA 2: 348–361.

45. de KlerkE, VenemaA, AnvarSY, GoemanJJ, HuO, et al. (2012) Poly(A) binding protein nuclear 1 levels affect alternative polyadenylation. Nucleic Acids Res 40: 9089–9101.

46. WangZ, GersteinM, SnyderM (2009) RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet 10: 57–63.

47. ClarkMB, MattickJS (2011) Long noncoding RNAs in cell biology. Semin Cell Dev Biol 22: 366–376.

48. GuttmanM, DonagheyJ, CareyBW, GarberM, GrenierJK, et al. (2011) lincRNAs act in the circuitry controlling pluripotency and differentiation. Nature 477: 295–300.

49. KhalilAM, GuttmanM, HuarteM, GarberM, RajA, et al. (2009) Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression. Proc Natl Acad Sci U S A 106: 11667–11672.

50. TsaiMC, ManorO, WanY, MosammaparastN, WangJK, et al. (2011) Long noncoding RNA as modular scaffold of histone modification complexes. Science 329: 689–693.

51. CesanaM, CacchiarelliD, LegniniI, SantiniT, SthandierO, et al. (2011) A long noncoding RNA controls muscle differentiation by functioning as a competing endogenous RNA. Cell 147: 358–369.

52. KarrethFA, TayY, PernaD, AlaU, TanSM, et al. (2011) In vivo identification of tumor- suppressive PTEN ceRNAs in an oncogenic BRAF-induced mouse model of melanoma. Cell 147: 382–395.

53. SalmenaL, PolisenoL, TayY, KatsL, PandolfiPP (2011) A ceRNA hypothesis: the Rosetta Stone of a hidden RNA language? Cell 146: 353–358.

54. SumazinP, YangX, ChiuHS, ChungWJ, IyerA, et al. (2011) An extensive microRNA-mediated network of RNA-RNA interactions regulates established oncogenic pathways in glioblastoma. Cell 147: 370–381.

55. TayY, KatsL, SalmenaL, WeissD, TanSM, et al. (2011) Coding-independent regulation of the tumor suppressor PTEN by competing endogenous mRNAs. Cell 147: 344–357.

56. GongC, MaquatLE (2011) lncRNAs transactivate STAU1-mediated mRNA decay by duplexing with 3′ UTRs via Alu elements. Nature 470: 284–288.

57. KinoT, HurtDE, IchijoT, NaderN, ChrousosGP (2010) Noncoding RNA gas5 is a growth arrest- and starvation-associated repressor of the glucocorticoid receptor. Sci Signal 3: ra8.

58. TripathiV, EllisJD, ShenZ, SongDY, PanQ, et al. (2010) The nuclear-retained noncoding RNA MALAT1 regulates alternative splicing by modulating SR splicing factor phosphorylation. Mol Cell 39: 925–938.

59. GuttmanM, GarberM, LevinJZ, DonagheyJ, RobinsonJ, et al. (2010) Ab initio reconstruction of cell type-specific transcriptomes in mouse reveals the conserved multi-exonic structure of lincRNAs. Nat Biotechnol 28: 503–510.

60. ClarkMB, JohnstonRL, Inostroza-PontaM, FoxAH, FortiniE, et al. (2012) Genome-wide analysis of long noncoding RNA stability. Genome Res

61. AndersonJT, WangX (2009) Nuclear RNA surveillance: no sign of substrates tailing off. Crit Rev Biochem Mol Biol 44: 16–24.

62. JiaH, WangX, LiuF, GuentherUP, SrinivasanS, et al. (2011) The RNA helicase Mtr4p modulates polyadenylation in the TRAMP complex. Cell 145: 890–901.

63. LebretonA, TomeckiR, DziembowskiA, SeraphinB (2008) Endonucleolytic RNA cleavage by a eukaryotic exosome. Nature 456: 993–996.

64. WlotzkaW, KudlaG, GrannemanS, TollerveyD (2011) The nuclear RNA polymerase II surveillance system targets polymerase III transcripts. Embo J 30: 1790–1803.

65. AllmangC, KufelJ, ChanfreauG, MitchellP, PetfalskiE, et al. (1999) Functions of the exosome in rRNA, snoRNA and snRNA synthesis. Embo J 18: 5399–5410.

66. LaCavaJ, HouseleyJ, SaveanuC, PetfalskiE, ThompsonE, et al. (2005) RNA degradation by the exosome is promoted by a nuclear polyadenylation complex. Cell 121: 713–724.

67. van HoofA, LennertzP, ParkerR (2000) Yeast exosome mutants accumulate 3′-extended polyadenylated forms of U4 small nuclear RNA and small nucleolar RNAs. Mol Cell Biol 20: 441–452.

68. ShiY, Di GiammartinoDC, TaylorD, SarkeshikA, RiceWJ, et al. (2009) Molecular architecture of the human pre-mRNA 3′ processing complex. Mol Cell 33: 365–376.

69. SeilaAC, CalabreseJM, LevineSS, YeoGW, RahlPB, et al. (2008) Divergent transcription from active promoters. Science 322: 1849–1851.

70. TaftRJ, GlazovEA, CloonanN, SimonsC, StephenS, et al. (2009) Tiny RNAs associated with transcription start sites in animals. Nat Genet 41: 572–578.

71. PrekerP, AlmvigK, ChristensenMS, ValenE, MapendanoCK, et al. (2011) PROMoter uPstream Transcripts share characteristics with mRNAs and are produced upstream of all three major types of mammalian promoters. Nucleic Acids Res 39: 7179–7193.

72. KissDL, AndrulisED (2011) The exozyme model: a continuum of functionally distinct complexes. Rna 17: 1–13.

73. WapinskiO, ChangHY (2011) Long noncoding RNAs and human disease. Trends Cell Biol 21: 354–361.

74. Askarian-AmiriME, CrawfordJ, FrenchJD, SmartCE, SmithMA, et al. (2011) SNORD-host RNA Zfas1 is a regulator of mammary development and a potential marker for breast cancer. Rna 17: 878–891.

75. UhlenM, OksvoldP, FagerbergL, LundbergE, JonassonK, et al. (2010) Towards a knowledge-based Human Protein Atlas. Nat Biotechnol 28: 1248–1250.

76. Abu-BakerA, LaganiereS, FanX, LaganiereJ, BraisB, et al. (2005) Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophy. Traffic 6: 766–779.

77. DominskiZ, MarzluffWF (2007) Formation of the 3′ end of histone mRNA: getting closer to the end. Gene 396: 373–390.

78. RobinsonJT, ThorvaldsdottirH, WincklerW, GuttmanM, LanderES, et al. (2011) Integrative genomics viewer. Nat Biotechnol 29: 24–26.

79. KentWJ, SugnetCW, FureyTS, RoskinKM, PringleTH, et al. (2002) The Human Genome Browser at UCSC. Genome Research 12: 996–1006.

80. QuinlanAR, HallIM (2010) BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 26: 841–842.

81. BachandF, BoisvertFM, CoteJ, RichardS, AutexierC (2002) The product of the survival of motor neuron (SMN) gene is a human telomerase-associated protein. Mol Biol Cell 13: 3192–3202.

82. AmaralPP, ClarkMB, GascoigneDK, DingerME, MattickJS (2011) lncRNAdb: a reference database for long noncoding RNAs. Nucleic Acids Res 39: D146–151.

83. HeS, LiuC, SkogerboG, ZhaoH, WangJ, et al. (2008) NONCODE v2.0: decoding the non-coding. Nucleic Acids Res 36: D170–172.

84. JiZ, LuoW, LiW, HoqueM, PanZ, et al. (2011) Transcriptional activity regulates alternative cleavage and polyadenylation. Mol Syst Biol 7: 534.

85. ZhangH, HuJ, RecceM, TianB (2005) PolyA_DB: a database for mammalian mRNA polyadenylation. Nucleic Acids Res 33: D116–120.

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Genetika Reprodukčná medicína

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PLOS Genetics


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