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Rescuing Alu: Recovery of Inserts Shows LINE-1 Preserves Alu Activity through A-Tail Expansion


Alu elements are trans-mobilized by the autonomous non-LTR retroelement, LINE-1 (L1). Alu-induced insertion mutagenesis contributes to about 0.1% human genetic disease and is responsible for the majority of the documented instances of human retroelement insertion-induced disease. Here we introduce a SINE recovery method that provides a complementary approach for comprehensive analysis of the impact and biological mechanisms of Alu retrotransposition. Using this approach, we recovered 226 de novo tagged Alu inserts in HeLa cells. Our analysis reveals that in human cells marked Alu inserts driven by either exogenously supplied full length L1 or ORF2 protein are indistinguishable. Four percent of de novo Alu inserts were associated with genomic deletions and rearrangements and lacked the hallmarks of retrotransposition. In contrast to L1 inserts, 5′ truncations of Alu inserts are rare, as most of the recovered inserts (96.5%) are full length. De novo Alus show a random pattern of insertion across chromosomes, but further characterization revealed an Alu insertion bias exists favoring insertion near other SINEs, highly conserved elements, with almost 60% landing within genes. De novo Alu inserts show no evidence of RNA editing. Priming for reverse transcription rarely occurred within the first 20 bp (most 5′) of the A-tail. The A-tails of recovered inserts show significant expansion, with many at least doubling in length. Sequence manipulation of the construct led to the demonstration that the A-tail expansion likely occurs during insertion due to slippage by the L1 ORF2 protein. We postulate that the A-tail expansion directly impacts Alu evolution by reintroducing new active source elements to counteract the natural loss of active Alus and minimizing Alu extinction.


Vyšlo v časopise: Rescuing Alu: Recovery of Inserts Shows LINE-1 Preserves Alu Activity through A-Tail Expansion. PLoS Genet 8(8): e32767. doi:10.1371/journal.pgen.1002842
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002842

Souhrn

Alu elements are trans-mobilized by the autonomous non-LTR retroelement, LINE-1 (L1). Alu-induced insertion mutagenesis contributes to about 0.1% human genetic disease and is responsible for the majority of the documented instances of human retroelement insertion-induced disease. Here we introduce a SINE recovery method that provides a complementary approach for comprehensive analysis of the impact and biological mechanisms of Alu retrotransposition. Using this approach, we recovered 226 de novo tagged Alu inserts in HeLa cells. Our analysis reveals that in human cells marked Alu inserts driven by either exogenously supplied full length L1 or ORF2 protein are indistinguishable. Four percent of de novo Alu inserts were associated with genomic deletions and rearrangements and lacked the hallmarks of retrotransposition. In contrast to L1 inserts, 5′ truncations of Alu inserts are rare, as most of the recovered inserts (96.5%) are full length. De novo Alus show a random pattern of insertion across chromosomes, but further characterization revealed an Alu insertion bias exists favoring insertion near other SINEs, highly conserved elements, with almost 60% landing within genes. De novo Alu inserts show no evidence of RNA editing. Priming for reverse transcription rarely occurred within the first 20 bp (most 5′) of the A-tail. The A-tails of recovered inserts show significant expansion, with many at least doubling in length. Sequence manipulation of the construct led to the demonstration that the A-tail expansion likely occurs during insertion due to slippage by the L1 ORF2 protein. We postulate that the A-tail expansion directly impacts Alu evolution by reintroducing new active source elements to counteract the natural loss of active Alus and minimizing Alu extinction.


Zdroje

1. LanderES, LintonLM, BirrenB, NusbaumC, ZodyMC, et al. (2001) Initial sequencing and analysis of the human genome. Nature 409: 860–921.

2. OvchinnikovI, TroxelAB, SwergoldGD (2001) Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion. Genome Res 11: 2050–2058.

3. DeiningerPL, BatzerMA (1999) Alu repeats and human disease. Mol Genet Metab 67: 183–193.

4. BelancioVP, HedgesDJ, DeiningerP (2008) Mammalian non-LTR retrotransposons: for better or worse, in sickness and in health. Genome Res 18: 343–358 gr.5558208 [pii];10.1101/gr.5558208 [doi].

5. WallaceMR, AndersenLB, SaulinoAM, GregoryPE, GloverTW, et al. (1991) A de novo Alu insertion results in neurofibromatosis type 1. Nature 353: 864–866.

6. KazazianHH, WongC, YoussoufianH, ScottAF, PhillipsDG, et al. (1988) Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. Nature 332: 164–166.

7. SymerDE, ConnellyC, SzakST, CaputoEM, CostGJ, et al. (2002) Human l1 retrotransposition is associated with genetic instability in vivo. Cell 110: 327–338.

8. GilbertN, Lutz-PriggeS, MoranJV (2002) Genomic deletions created upon LINE-1 retrotransposition. Cell 110: 315–325.

9. GilbertN, LutzS, MorrishTA, MoranJV (2005) Multiple fates of L1 retrotransposition intermediates in cultured human cells. Mol Cell Biol 25: 7780–7795.

10. OstertagEM, KazazianHHJr (2001) Twin priming: a proposed mechanism for the creation of inversions in l1 retrotransposition. Genome Res 11: 2059–2065.

11. MorrishTA, Garcia-PerezJL, StamatoTD, TaccioliGE, SekiguchiJ, et al. (2007) Endonuclease-independent LINE-1 retrotransposition at mammalian telomeres. Nature 446: 208–212 nature05560 [pii];10.1038/nature05560 [doi].

12. SuzukiJ, YamaguchiK, KajikawaM, IchiyanagiK, AdachiN, et al. (2009) Genetic evidence that the non-homologous end-joining repair pathway is involved in LINE retrotransposition. PLoS Genet 5: e1000461 doi:10.1371/journal.pgen.1000461.

13. El SawyM, KaleSP, DuganC, NguyenTQ, BelancioV, et al. (2005) Nickel stimulates L1 retrotransposition by a post-transcriptional mechanism. J Mol Biol 354: 246–257.

14. CallinanPA, WangJ, HerkeSW, GarberRK, LiangP, et al. (2005) Alu retrotransposition-mediated deletion. J Mol Biol 348: 791–800.

15. XingJ, ZhangY, HanK, SalemAH, SenSK, et al. (2009) Mobile elements create structural variation: analysis of a complete human genome. Genome Res 19: 1516–1526 gr.091827.109 [pii];10.1101/gr.091827.109 [doi].

16. HanK, SenSK, WangJ, CallinanPA, LeeJ, et al. (2005) Genomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineages. Nucleic Acids Res 33: 4040–4052.

17. DewannieuxM, EsnaultC, HeidmannT (2003) LINE-mediated retrotransposition of marked Alu sequences. Nat Genet 35: 41–48.

18. HaganCR, SheffieldRF, RudinCM (2003) Human Alu element retrotransposition induced by genotoxic stress. Nat Genet 35: 219–220.

19. DewannieuxM, HeidmannT (2005) L1-mediated retrotransposition of murine B1 and B2 SINEs recapitulated in cultured cells. J Mol Biol 349: 241–247.

20. IskowRC, McCabeMT, MillsRE, ToreneS, PittardWS, et al. (2010) Natural mutagenesis of human genomes by endogenous retrotransposons. Cell 141: 1253–1261 S0092-8674(10)00556-8 [pii];10.1016/j.cell.2010.05.020 [doi].

21. BaillieJK, BarnettMW, UptonKR, GerhardtDJ, RichmondTA, et al. (2011) Somatic retrotransposition alters the genetic landscape of the human brain. Nature nature10531 [pii];10.1038/nature10531 [doi].

22. StalkerDM, KolterR, HelinskiDR (1982) Plasmid R6K DNA replication : I. Complete nucleotide sequence of an autonomously replicating segment. Journal of Molecular Biology 161: 33–43.

23. ShaffermanA, HelinskiDR (1983) Structural properties of the beta origin of replication of plasmid R6K. J Biol Chem 258: 4083–4090.

24. ComeauxMS, Roy-EngelAM, HedgesDJ, DeiningerPL (2009) Diverse cis factors controlling Alu retrotransposition: What causes Alu elements to die? Genome Res 19: 545–555.

25. WallaceN, WagstaffBJ, DeiningerPL, Roy-EngelAM (2008) LINE-1 ORF1 protein enhances Alu SINE retrotransposition. Gene 419: 1–6.

26. JurkaJ (1997) Sequence patterns indicate an enzymatic involvement in integration of mammalian retroposons. Proc Natl Acad Sci U S A 94: 1872–1877.

27. CostGJ, BoekeJD (1998) Targeting of human retrotransposon integration is directed by the specificity of the L1 endonuclease for regions of unusual DNA structure. Biochemistry 37: 18081–18093.

28. FengQ, MoranJV, KazazianHHJr, BoekeJD (1996) Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition. Cell 87: 905–916.

29. KojimaKK (2010) Different integration site structures between L1 protein-mediated retrotransposition in cis and retrotransposition in trans. Mob DNA 1: 17 1759-8753-1-17 [pii];10.1186/1759-8753-1-17 [doi].

30. DeChiaraTM, BrosiusJ (1987) Neural BC1 RNA: cDNA clones reveal nonrepetitive sequence content. Proc Natl Acad Sci 84: 2624–2628.

31. KramerovDA, GrigoryanAA, RyskovAP, GeorgievGP (1979) Long double-stranded sequences (dsRNA-B) of nuclear pre-mRNA consist of a few highly abundant classes of sequences: evidence from DNA cloning experiments. Nucleic Acids Res 6: 697–713.

32. KrayevAS, MarkushevaTV, KramerovDA, RyskovAP, SkryabinKG, et al. (1982) Ubiquitous transposon-like repeats B1 and B2 of the mouse genome: B2 sequencing. Nucleic Acids Res 10: 7461–7475.

33. WaterstonRH, Lindblad-TohK, BirneyE, RogersJ, AbrilJF, et al. (2002) Initial sequencing and comparative analysis of the mouse genome. Nature 420: 520–562.

34. HayakawaT, SattaY, GagneuxP, VarkiA, TakahataN (2001) Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene. Proc Natl Acad Sci U S A 98: 11399–11404 10.1073/pnas.191268198 [doi];191268198 [pii].

35. Morrish TA, Moran JV (2001) Endonuclease-Independent L1 Retrotransposition. American Society of Human Genetics (ASHG) 51st Annual Meeting Abstracts.

36. GasiorSL, PrestonG, HedgesDJ, GilbertN, MoranJV, et al. (2006) Characterization of pre-insertion loci of de novo L1 insertions. Gene

37. SelaN, MerschB, Gal-MarkN, Lev-MaorG, Hotz-WagenblattA, et al. (2007) Comparative analysis of transposed element insertion within human and mouse genomes reveals Alu's unique role in shaping the human transcriptome. Genome Biol 8: R127 gb-2007-8-6-r127 [pii];10.1186/gb-2007-8-6-r127 [doi].

38. SorekR, AstG, GraurD (2002) Alu-Containing Exons are Alternatively Spliced. Genome Research 12: 1060–1067.

39. KvikstadEM, MakovaKD (2010) The (r)evolution of SINE versus LINE distributions in primate genomes: sex chromosomes are important. Genome Res 20: 600–613 gr.099044.109 [pii];10.1101/gr.099044.109 [doi].

40. BarakM, LevanonEY, EisenbergE, PazN, RechaviG, et al. (2009) Evidence for large diversity in the human transcriptome created by Alu RNA editing. Nucleic Acids Res 37: 6905–6915 gkp729 [pii];10.1093/nar/gkp729 [doi].

41. LevanonEY, EisenbergE, YelinR, NemzerS, HalleggerM, et al. (2004) Systematic identification of abundant A-to-I editing sites in the human transcriptome. Nat Biotechnol 22: 1001–1005 10.1038/nbt996 [doi];nbt996 [pii].

42. KimDD, KimTT, WalshT, KobayashiY, MatiseTC, et al. (2004) Widespread RNA editing of embedded alu elements in the human transcriptome. Genome Res 14: 1719–1725 10.1101/gr.2855504 [doi];14/9/1719 [pii].

43. AthanasiadisA, RichA, MaasS (2004) Widespread A-to-I RNA editing of Alu-containing mRNAs in the human transcriptome. PLoS Biol 2: e391 doi:10.1371/journal.pbio.0020391.

44. BogerdHP, WiegandHL, HulmeAE, Garcia-PerezJL, O'sheaKS, et al. (2006) Cellular inhibitors of long interspersed element 1 and Alu retrotransposition. Proc Natl Acad Sci U S A 103: 8780–8785.

45. HulmeAE, BogerdHP, CullenBR, MoranJV (2007) Selective inhibition of Alu retrotransposition by APOBEC3G. Gene 390: 199–205.

46. SiepelA, BejeranoG, PedersenJS, HinrichsAS, HouM, et al. (2005) Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. Genome Res 15: 1034–1050 gr.3715005 [pii];10.1101/gr.3715005 [doi].

47. EllerCD, RegelsonM, MerrimanB, NelsonS, HorvathS, et al. (2007) Repetitive sequence environment distinguishes housekeeping genes. Gene 390: 153–165 S0378-1119(06)00620-2 [pii];10.1016/j.gene.2006.09.018 [doi].

48. KimTM, JungYC, RhyuMG (2004) Alu and L1 retroelements are correlated with the tissue extent and peak rate of gene expression, respectively. J Korean Med Sci 19: 783–792 200412783 [pii].

49. WitherspoonD, WatkinsW, ZhangY, XingJ, TolpinrudW, et al. (2009) Alu repeats increase local recombination rates. BMC Genomics 10: 530.

50. MyersS, FreemanC, AutonA, DonnellyP, McVeanG (2008) A common sequence motif associated with recombination hot spots and genome instability in humans. Nat Genet 40: 1124–1129 10.1038/ng.213 [doi].

51. SellisD, ProvataA, AlmirantisY (2007) Alu and LINE1 distributions in the human chromosomes: evidence of global genomic organization expressed in the form of power laws. Mol Biol Evol 24: 2385–2399 msm181 [pii];10.1093/molbev/msm181 [doi].

52. El SawyM, DeiningerP (2005) Tandem insertions of Alu elements. Cytogenet Genome Res 108: 58–62.

53. HackenbergM, Bernaola-GalvanP, CarpenaP, OliverJL (2005) The biased distribution of Alus in human isochores might be driven by recombination. J Mol Evol 365–377 10.1007/s00239-004-0197-2 [doi].

54. GuW, ZhangF, LupskiJR (2008) Mechanisms for human genomic rearrangements. Pathogenetics 1: 4 1755-8417-1-4 [pii];10.1186/1755-8417-1-4 [doi].

55. McVeanG (2010) What drives recombination hotspots to repeat DNA in humans? Philos Trans R Soc Lond B Biol Sci 365: 1213–1218 365/1544/1213 [pii];10.1098/rstb.2009.0299 [doi].

56. SenSK, HanK, WangJ, LeeJ, WangH, et al. (2006) Human Genomic Deletions Mediated by Recombination between Alu Elements. Am J Hum Genet 79: 41–53.

57. SrikantaD, SenSK, ConlinEM, BatzerMA (2009) Internal priming: an opportunistic pathway for L1 and Alu retrotransposition in hominins. Gene 448: 233–241 S0378-1119(09)00323-0 [pii];10.1016/j.gene.2009.05.014 [doi].

58. SrikantaD, SenSK, HuangCT, ConlinEM, RhodesRM, et al. (2009) An alternative pathway for Alu retrotransposition suggests a role in DNA double-strand break repair. Genomics 93: 205–212 S0888-7543(08)00231-0 [pii];10.1016/j.ygeno.2008.09.016 [doi].

59. WestN, Roy-EngelA, ImatakaH, SonenbergN, DeiningerP (2002) Shared Protein Components of SINE RNPs. J Mol Biol 321: 423–432.

60. MuddashettyR, KhanamT, KondrashovA, BundmanM, IacoangeliA, et al. (2002) Poly(A)-binding Protein is Associated with Neuronal BC1 and BC200 Ribonucleoprotein Particles. J Mol Biol 321: 433–445.

61. ChaboissierMC, FinneganD, BuchetonA (2000) Retrotransposition of the I factor, a non-long terminal repeat retrotransposon of Drosophila, generates tandem repeats at the 3′ end. Nucleic Acids Res 28: 2467–2472.

62. CohnM, BlackburnEH (1995) Telomerase in yeast. Science 269: 396–400.

63. PrescottJ, BlackburnEH (1997) Telomerase RNA mutations in Saccharomyces cerevisiae alter telomerase action and reveal nonprocessivity in vivo and in vitro. Genes Dev 11: 528–540.

64. BlackburnEH (2005) Telomeres and telomerase: their mechanisms of action and the effects of altering their functions. Febs Lett 579: 859–862 S0014-5793(04)01426-7 [pii];10.1016/j.febslet.2004.11.036 [doi].

65. CollinsK (1999) Ciliate telomerase biochemistry. Annu Rev Biochem 68: 187–218 10.1146/annurev.biochem.68.1.187 [doi].

66. SinghSM, Steinberg-NeifachO, MianIS, LueNF (2002) Analysis of telomerase in Candida albicans: potential role in telomere end protection. Eukaryot Cell 1: 967–977.

67. KoperaHC, MoldovanJB, MorrishTA, Garcia-PerezJL, MoranJV (2011) Similarities between long interspersed element-1 (LINE-1) reverse transcriptase and telomerase. Proc Natl Acad Sci U S A 1100275108 [pii];10.1073/pnas.1100275108 [doi].

68. LuanDD, EickbushTH (1995) RNA template requirements for target DNA-primed reverse transcription by the R2 retrotransposable element. Mol Cell Biol 15: 3882–3891.

69. BennettEA, KellerH, MillsRE, SchmidtS, MoranJV, et al. (2008) Active Alu retrotransposons in the human genome. Genome Res 18: 1875–1883.

70. DewannieuxM, HeidmannT (2005) Role of poly(A) tail length in Alu retrotransposition. Genomics 86: 378–381.

71. EconomouEP, BergenAW, WarrenAC, AntonarakisSE (1990) The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome. Proc Natl Acad Sci, USA 87: 2951–2954.

72. Roy-EngelAM, SalemAH, OyeniranOO, DeiningerL, HedgesDJ, et al. (2002) Active alu element “A-Tails”: size does matter. Genome Res 12: 1333–1344.

73. RinehartTA, GrahnRA, WichmanHA (2005) SINE extinction preceded LINE extinction in sigmodontine rodents: implications for retrotranspositional dynamics and mechanisms. Cytogenet Genome Res 110: 416–425.

74. HanK, XingJ, WangH, HedgesDJ, GarberRK, et al. (2005) Under the genomic radar: the stealth model of Alu amplification. Genome Res 15: 655–664.

75. WagstaffBJ, BarnerssoiM, Roy-EngelAM (2011) Evolutionary conservation of the functional modularity of primate and murine LINE-1 elements. PLoS ONE 6: e19672 doi:10.1371/journal.pone.0019672.

76. KroutterEN, BelancioVP, WagstaffBJ, Roy-EngelAM (2009) The RNA Polymerase Dictates ORF1 Requirement and Timing of LINE and SINE Retrotransposition. PLoS Genet 5: e1000458 doi:10.1371/journal.pgen.1000458.

77. OrioliA, PascaliC, QuartararoJ, DiebelKW, PrazV, et al. (2011) Widespread occurrence of non-canonical transcription termination by human RNA polymerase III. Nucleic Acids Res 39: 5499–5512 gkr074 [pii];10.1093/nar/gkr074 [doi].

78. RoyAM, WestNC, RaoA, AdhikariP, AlemánC, et al. (2000) Upstream flanking sequences and transcription of SINEs. J Mol Biol 302: 17–25.

79. MacvilleM, SchrockE, Padilla-NashH, KeckC, GhadimiBM, et al. (1999) Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping. Cancer Res 59: 141–150.

80. Hollander M. and Wolfe, D A. (1999) Nonparametric Statistical Methods. New York: Wiley & Sons.

81. R Development Core Team (2008) R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing.

82. Perepelitsa-BelancioV, DeiningerPL (2003) RNA truncation by premature polyadenylation attenuates human mobile element activity. Nat Genet 35: 363–366.

83. CrooksGE, HonG, ChandoniaJM, BrennerSE (2004) WebLogo: a sequence logo generator. Genome Res 14: 1188–1190 10.1101/gr.849004 [doi];14/6/1188 [pii].

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