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Comparative analysis of transposed element insertion within human and mouse genomes reveals Alu's unique role in shaping the human transcriptome

Noa Sela, Britta Mersch, Nurit Gal-Mark and 3 more

Genome Biology · 2007 · CC BY

doi:10.1186/gb-2007-8-6-r127

Abstract

Background. Transposed elements (TEs) have a substantial impact on mammalian evolution and are involved in numerous genetic diseases. We compared the impact of TEs on the human transcriptome and the mouse transcriptome.

Results. We compiled a dataset of all TEs in the human and mouse genomes, identifying 3,932,058 and 3,122,416 TEs, respectively. We than extracted TEs located within human and mouse genes and, surprisingly, we found that 60% of TEs in both human and mouse are located in intronic sequences, even though introns comprise only 24% of the human genome. All TE families in both human and mouse can exonize. TE families that are shared between human and mouse exhibit the same percentage of TE exonization in the two species, but the exonization level of Alu, a primate-specific retroelement, is significantly greater than that of other TEs within the human genome, leading to a higher level of TE exonization in human than in mouse (1,824 exons compared with 506 exons, respectively). We detected a primate-specific mechanism for intron gain, in which Alu insertion into an exon creates a new intron located in the 3' untranslated region (termed 'intronization'). Finally, the insertion of TEs into the first and last exons of a gene is more frequent in human than in mouse, leading to longer exons in human.

Conclusion. Our findings reveal many effects of TEs on these two transcriptomes. These effects are substantially greater in human than in mouse, which is due to the presence of Alu elements in human.

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References 60

  1. 1.

    Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, et al. Initial sequencing and analysis of the human genome. Nature. 2001;409:860-921.

    Not in our library10.1038/35057062

  2. 2.

    Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, et al. Initial sequencing and comparative analysis of the mouse genome. Nature. 2002;420:520-562.

    Not in our library10.1038/nature01262

  3. 3.

    Sorek R, Ast G, Graur D. Alu-containing exons are alternatively spliced. Genome Res. 2002;12:1060-1067.

    Not in our library10.1101/gr.229302

  4. 4.

    Lev-Maor G, Sorek R, Shomron N, Ast G. The birth of an alternatively spliced exon: 3' splice-site selection in Alu exons. Science. 2003;300:1288-1291.

    Not in our library10.1126/science.1082588

  5. 5.

    Sorek R, Lev-Maor G, Reznik M, Dagan T, Belinky F, Graur D, Ast G. Minimal conditions for exonization of intronic sequences: 5' splice site formation in alu exons. Mol Cell. 2004;14:221-231.

    Not in our library10.1016/s1097-2765(04)00181-9

  6. 6.

    Brosius J, Gould SJ. On 'genomenclature': a comprehensive (and respectful) taxonomy for pseudogenes and other 'junk DNA'. Proc Natl Acad Sci USA. 1992;89:10706-10710.

    Not in our library10.1073/pnas.89.22.10706

  7. 7.

    Gotea V, Makalowski W. Do transposable elements really contribute to proteomes? Trends Genet. 2006;22:260-267.

    Not in our library10.1016/j.tig.2006.03.006

  8. 8.

    Hasler J, Strub K. Alu elements as regulators of gene expression. Nucleic Acids Res. 2006;34:5491-5497.

    Not in our library10.1093/nar/gkl706

  9. 9.

    Hedges DJ, Batzer MA. From the margins of the genome: mobile elements shape primate evolution. Bioessays. 2005;27:785-794.

    Not in our library10.1002/bies.20268

  10. 10.

    Krull M, Brosius J, Schmitz J. Alu-SINE exonization: en route to protein-coding function. Mol Biol Evol. 2005;22:1702-1711.

    Not in our library10.1093/molbev/msi164

  11. 11.

    Ast G. How did alternative splicing evolve? Nat Rev Genet. 2004;5:773-782.

    Not in our library10.1038/nrg1451

  12. 12.

    Gerber A, O'Connell MA, Keller W. Two forms of human double-stranded RNA-specific editase 1 (hRED1) generated by the insertion of an Alu cassette. Rna. 1997;3:453-463.

    Not in our library

  13. 13.

    Bejerano G, Lowe CB, Ahituv N, King B, Siepel A, Salama SR, Rubin EM, Kent WJ, Haussler D. A distal enhancer and an ultraconserved exon are derived from a novel retroposon. Nature. 2006;441:87-90.

    Not in our library10.1038/nature04696

  14. 14.

    Modrek B, Lee CJ. Alternative splicing in the human, mouse and rat genomes is associated with an increased frequency of exon creation and/or loss. Nat Genet. 2003;34:177-180.

    Not in our library10.1038/ng1159

  15. 15.

    Ferlini A, Galie N, Merlini L, Sewry C, Branzi A, Muntoni F. A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy. Am J Hum Genet. 1998;63:436-446.

    Not in our library10.1086/301952

  16. 16.
  17. 17.

    Brosius J. Disparity, causation, adaptation, exaptation, and contingency at the genome level. Paleobiology. 2005;31:1-16.

    Not in our library10.1666/0094-8373(2005)031[0001:daebac]2.0.co;2

  18. 18.

    Sironi M, Menozzi G, Comi GP, Bresolin N, Cagliani R, Pozzoli U. Fixation of conserved sequences shapes human intron size and influences transposon-insertion dynamics. Trends Genet. 2005;21:484-488.

    Not in our library10.1016/j.tig.2005.06.009

  19. 19.

    Sironi M, Menozzi G, Comi GP, Cereda M, Cagliani R, Bresolin N, Pozzoli U. Gene function and expression level influence the insertion/fixation dynamics of distinct transposon families in mammalian introns. Genome Biol. 2006;7:R120.

    Not in our library10.1186/gb-2006-7-12-r120

  20. 20.

    Zhuo D, Madden R, Elela SA, Chabot B. Modern origin of numerous alternatively spliced human introns from tandem arrays. Proc Natl Acad Sci USA. 2007;104:882-886.

    Not in our library10.1073/pnas.0604777104

  21. 21.

    Iwamoto M, Maekawa M, Saito A, Higo H, Higo K. Evolutionary relationship of plant catalase genes inferred from exon-intron structures: isozyme divergence after the separation of monocots and dicots. Theor Appl Genet. 1998;97:9-19.

    Not in our library10.1007/s001220050861

  22. 22.

    Roy SW. The origin of recent introns: transposons? Genome Biol. 2004;5:251.

    Not in our library10.1186/gb-2004-5-12-251

  23. 23.

    Coulombe-Huntington J, Majewski J. Characterization of intron loss events in mammals. Genome Res. 2007;17:23-32.

    Not in our library10.1101/gr.5703406

  24. 24.

    Roy SW, Fedorov A, Gilbert W. Large-scale comparison of intron positions in mammalian genes shows intron loss but no gain. Proc Natl Acad Sci USA. 2003;100:7158-7162.

    Not in our library10.1073/pnas.1232297100

  25. 25.

    Pace JK, Feschotte C. The evolutionary history of human DNA transposons: evidence for intense activity in the primate lineage. Genome Res. 2007;17:422-432.

    Not in our library10.1101/gr.5826307

  26. 26.

    Kriegs JO, Churakov G, Jurka J, Brosius J, Schmitz J. Evolutionary history of 7SL RNA-derived SINEs in Supraprimates. Trends Genet. 2007;23:158-161.

    Not in our library10.1016/j.tig.2007.02.002

  27. 27.

    Wang Z, Lo HS, Yang H, Gere S, Hu Y, Buetow KH, Lee MP. Computational analysis and experimental validation of tumor-associated alternative RNA splicing in human cancer. Cancer Res. 2003;63:655-657.

    Not in our library

  28. 28.

    UCSC genome browser.

    Not in our library

  29. 29.

    Ponjavic J, Ponting CP, Lunter G. Functionality or transcriptional noise? Evidence for selection within long noncoding RNAs. Genome Res. 2007;17:556-565.

    Not in our library10.1101/gr.6036807

  30. 30.

    Xu Q, Modrek B, Lee C. Genome-wide detection of tissue-specific alternative splicing in the human transcriptome. Nucleic Acids Res. 2002;30:3754-3766.

    Not in our library10.1093/nar/gkf492

  31. 31.

    Xu Q, Lee C. Discovery of novel splice forms and functional analysis of cancer-specific alternative splicing in human expressed sequences. Nucleic Acids Res. 2003;31:5635-5643.

    Not in our library10.1093/nar/gkg786

  32. 32.

    Pollard AJ, Krainer AR, Robson SC, Europe-Finner GN. Alternative splicing of the adenylyl cyclase stimulatory G-protein G alpha(s) is regulated by SF2/ASF and heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1) and involves the use of an unusual TG 3'-splice Site. J Biol Chem. 2002;277:15241-15251.

    Not in our library10.1074/jbc.m109046200

  33. 33.

    Breglia SA, Slamovits CH, Leander BS. Phylogeny of phagotrophic euglenids (Euglenozoa) as inferred from hsp90 gene sequences. J Eukaryot Microbiol. 2007;54:86-92.

    Not in our library10.1111/j.1550-7408.2006.00233.x

  34. 34.

    Lei H, Vorechovsky I. Identification of splicing silencers and enhancers in sense Alus: a role for pseudoacceptors in splice site repression. Mol Cell Biol. 2005;25:6912-6920.

    Not in our library10.1128/mcb.25.16.6912-6920.2005

  35. 35.

    Hulo N, Bairoch A, Bulliard V, Cerutti L, De Castro E, Langendijk-Genevaux PS, Pagni M, Sigrist CJ. The PROSITE database. Nucleic Acids Res. 2006;34:D227-230.

    Not in our library10.1093/nar/gkj063

  36. 36.

    PROSITE.

    Not in our library

  37. 37.

    Xing Y, Lee C. Alternative splicing and RNA selection pressure: evolutionary consequences for eukaryotic genomes. Nat Rev Genet. 2006;7:499-509.

    Not in our library10.1038/nrg1896

  38. 38.

    Deininger PL, Moran JV, Batzer MA, Kazazian HH. Mobile elements and mammalian genome evolution. Curr Opin Genet Dev. 2003;13:651-658.

    Not in our library10.1016/j.gde.2003.10.013

  39. 39.

    Han JS, Boeke JD. LINE-1 retrotransposons: modulators of quantity and quality of mammalian gene expression? Bioessays. 2005;27:775-784.

    Not in our library10.1002/bies.20257

  40. 40.

    Han JS, Szak ST, Boeke JD. Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes. Nature. 2004;429:268-274.

    Not in our library10.1038/nature02536

All 60 references

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