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Analysis of 5′ junctions of human LINE-1 and Alu retrotransposons suggests an alternative model for 5′-end attachment requiring microhomology-mediated end-joining
Open accessAbstract
Insertion of the human non-LTR retrotransposon LINE-1 (L1) into chromosomal DNA is thought to be initiated by a mechanism called target-primed reverse transcription (TPRT). This mechanism readily accounts for the attachment of the 3′-end of an L1 copy to the genomic target, but the subsequent integration steps leading to the attachment of the 5′-end to the chromosomal DNA are still cause for speculation. By applying bioinformatics to analyze the 5′ junctions of recent L1 insertions in the human genome, we provide evidence that L1 uses at least two distinct mechanisms to link the 5′-end of the nascent L1 copy to its genomic target. While 5′-truncated L1 elements show a statistically significant preference for short patches of overlapping nucleotides between their target site and the point of truncation, full-length insertions display no distinct bias for such microhomologies at their 5′-ends. In a second genome-wide approach, we analyzed Alu elements to examine whether these nonautonomous retrotransposons, which are thought to be mobilized through L1 proteins, show similar characteristics. We found that Alu elements appear to be predominantly integrated via a pathway not involving overlapping nucleotides. The results indicate that a cellular nonhomologous DNA end-joining pathway may resolve intermediates from incomplete L1 retrotransposition events and thus lead to 5′ truncations.
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“Computational analyses of de novo L1 integrations and genomic L1 integrations have shown that most integrations proceed through a microhomology process for priming L1 DNA synthesis.9”
From The Human LINE-1 Retrotransposon Creates DNA Double-strand Breaks (2006) · cites this paper as [9]
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Cites
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216
Alu repeats and human genomic diversity
Batzer, M., & Deininger, P. (2002) · Nature reviews genetics · doi:10.1038/nrg798 · Cited by 1,522
Luan, D. D., Korman, M. H., Jakubczak, J. L., & Eickbush, T. H. (1993) · Cell · doi:10.1016/0092-8674(93)90078-5 · Cited by 1,173
Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition
Feng, Q., Moran, J. V., Kazazian, H. H., & Boeke, J. D. (1996) · Cell · doi:10.1016/s0092-8674(00)81997-2 · Cited by 1,139
LINE-mediated retrotransposition of marked Alu sequences
Dewannieux, M., Esnault, C., & Heidmann, T. (2003) · Nature Genetics · doi:10.1038/ng1223 · Cited by 1,026
Human LINE retrotransposons generate processed pseudogenes
Esnault, C., Maestre, J., & Heidmann, T. (2000) · Nature Genetics · doi:10.1038/74184 · Cited by 835
Biology of Mammalian L1 Retrotransposons
Ostertag, E. M., & Kazazian, H. H. (2001) · Annual Review of Genetics · doi:10.1146/annurev.genet.35.102401.091032 · Cited by 782
Reverse Transcriptase Encoded by a Human Transposable Element
Mathias, S. L., Scott, A. F., Kazazian, H. H., Boeke, J. D., & Gabriel, A. (1991) · Science · doi:10.1126/science.1722352 · Cited by 774
The age and evolution of non-LTR retrotransposable elements
Malik, H. S., Burke, W. D., & Eickbush, T. H. (1999) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a026164 · Cited by 587
Sequence patterns indicate an enzymatic involvement in integration of mammalian retroposons
Jurka, J. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.5.1872 · Cited by 560
Human L1 element target‐primed reverse transcription in vitro
Cost, G. J., Feng, Q., Jacquier, A., & Boeke, J. D. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf592 · Cited by 519
Mechanisms of DNA double-strand break repair and their potential to induce chromosomal aberrations
Pfeiffer, P. (2000) · Mutagenesis · doi:10.1093/mutage/15.4.289 · Cited by 489
DNA repair mediated by endonuclease-independent LINE-1 retrotransposition
Morrish, T. A., Gilbert, N., Myers, J. S., Vincent, B. J., Stamato, T. D., Taccioli, G. E., Batzer, M. A., & Moran, J. V. (2002) · Nature Genetics · doi:10.1038/ng898 · Cited by 488
Self-citationHuman L1 Retrotransposition Is Associated with Genetic Instability In Vivo
Symer, D. E., Connelly, C. J., Szak, S. T., Caputo, E. M., Cost, G. J., Parmigiani, G., & Boeke, J. D. (2002) · Cell · doi:10.1016/s0092-8674(02)00839-5 · Cited by 479
Genomic Deletions Created upon LINE-1 Retrotransposition
Gilbert, N., Lutz-Prigge, S., & Moran, J. V. (2002) · Cell · doi:10.1016/s0092-8674(02)00828-0 · Cited by 474
Isolation of an Active Human Transposable Element
Dombroski, B. A., Mathias, S. L., Nanthakumar, E. J., Scott, A. F., & Kazazian, H. H. (1991) · Science · doi:10.1126/science.1662412 · Cited by 455
Many human L1 elements are capable of retrotransposition
Sassaman, D. M., Dombroski, B. A., Moran, J. V., Kimberland, M. L., Naas, T., DeBerardinis, R. J., Gabriel, A., Swergold, G. D., & Kazazian, H. H. (1997) · Nature Genetics · doi:10.1038/ng0597-37 · Cited by 452
Role of the non‐homologous DNA end joining pathway in the early steps of retroviral infection
Li, L., Olvera, J. M., Yoder, K., Mitchell, R., Butler, S., Lieber, M., Martin, S. L., & Bushman, F. D. (2001) · EMBO Journal · doi:10.1093/emboj/20.12.3272 · Cited by 386
Ancestral, Mammalian-wide Subfamilies of LINE-1 Repetitive Sequences
Smit, A. F. A., Tóth, G. J., Riggs, A. D., & Jurka, J. (1995) · Journal of Molecular Biology · doi:10.1006/jmbi.1994.0095 · Cited by 384
Nucleic Acid Chaperone Activity of the ORF1 Protein from the Mouse LINE-1 Retrotransposon
Martin, S. L., & Bushman, F. D. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.2.467-475.2001 · Cited by 368
Mechanisms of nonhomologous recombination in mammalian cells.
Roth, D. B., Porter, T. N., & Wilson, J. H. (1985) · Molecular and Cellular Biology · doi:10.1128/mcb.5.10.2599 · Cited by 314
L1 (LINE-1) Retrotransposon Evolution and Amplification in Recent Human History
Boissinot, S., Chevret, P., & Furano, A. V. (2000) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a026372 · Cited by 312
Unit-Length Line-1 Transcripts in Human Teratocarcinoma Cells
Skowroński, J., Fanning, T. G., & Singer, M. (1988) · Molecular and Cellular Biology · doi:10.1128/mcb.8.4.1385 · Cited by 301
Twin Priming: A Proposed Mechanism for the Creation of Inversions in L1 RetrotranspositionPreprint
Ostertag, E. M., & Kazazian, H. H. (2001) · Genome Research · doi:10.1101/gr.205701 · Cited by 255
Capture of retrotransposon DNA at the sites of chromosomal double-strand breaks
Moore, J. K., & Haber, J. E. (1996) · Nature · doi:10.1038/383644a0 · Cited by 251
Double-strand break repair in Ku86- and XRCC4-deficient cells
Kabotyanski, E. B., Gomelsky, L., Han, J.-O., Roth, D. B., & Stamato, T. D. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.23.5333 · Cited by 244
Cost, G. J., & Boeke, J. D. (1998) · Biochemistry · doi:10.1021/bi981858s · Cited by 242
Retrotransposon reverse-transcriptase-mediated repair of chromosomal breaks
Teng, S., Kim, B., & Gabriel, A. (1996) · Nature · doi:10.1038/383641a0 · Cited by 238
Molecular archeology of L1 insertions in the human genome
Szak, S. T., Pickeral, O. K., Makalowski, W., Boguski, M. S., Landsman, D., & Boeke, J. D. (2002) · Genome Biology · doi:10.1186/gb-2002-3-10-research0052 · Cited by 230 · cited 15×
“Only 15% of all intact L1 insertions flanked by target site duplications (TSDs) represent full-length insertions, 85% are 5 truncated, and 19% are both 5 -truncated and 5 -inverted (Szak et al. 2002).”
BackgroundMethodInfluentialA YY1-binding site is required for accurate human LINE-1 transcription initiation
Athanikar, J. N. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh698 · Cited by 200
Schwarz‐Sommer, Z., Leclercq, L., Göbel, E., & Saedler, H. (1987) · The EMBO Journal · doi:10.1002/j.1460-2075.1987.tb02727.x · Cited by 196
Kolosha, V. O., & Martin, S. L. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.19.10155 · Cited by 175
Alu transcripts: cytoplasmic localisation and regulation by DNA methylation
Liu, W.-M., Maraia, R. J., Rubin, C. M., & Schmid, C. W. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.6.1087 · Cited by 163
A Comprehensive Analysis of Recently Integrated Human Ta L1 Elements
Myers, J. S., Vincent, B. J., Udall, H., Watkins, W. S., Morrish, T. A., Kilroy, G. E., Swergold, G. D., Henke, J., Henke, L., Moran, J. V., et al. (2002) · The American Journal of Human Genetics · doi:10.1086/341718 · Cited by 158
Self-citationFanning, T. G., & Singer, M. (1987) · Nucleic Acids Research · doi:10.1093/nar/15.5.2251 · Cited by 136
Sequence analysis of a Kpnl family member near the 3′ end of human β-globin gene
Hattori, M., Hidaka, S., & Sakaki, Y. (1985) · Nucleic Acids Research · doi:10.1093/nar/13.21.7813 · Cited by 133
Kolosha, V. O., & Martin, S. L. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210487200 · Cited by 131
Mechanisms of Nonhomologous Recombination in Mammalian Cells
Roth, D. B., Porter, T. N., & Wilson, J. H. (1985) · Molecular and Cellular Biology · doi:10.1128/mcb.5.10.2599-2607.1985 · Cited by 129
Transcriptional analysis of interspersed repetitive polymerase III transcription units in human DNA
Elder, J. T., Pan, J., Duncan, C. H., & Weissman, S. M. (1981) · Nucleic Acids Research · doi:10.1093/nar/9.5.1171 · Cited by 125
Restraining the V(D)J recombinase
Roth, D. B. (2003) · Nature reviews. Immunology · doi:10.1038/nri1152 · Cited by 123
Bentley, J. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh842 · Cited by 120
Dombroski, B. A., Scott, A. F., & Kazazian, H. H. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.14.6513 · Cited by 119
Fuhrman, S. A., Deininger, P. L., LaPorte, P., Friedmann, T., & Geiduschek, E. P. (1981) · Nucleic Acids Research · doi:10.1093/nar/9.23.6439 · Cited by 119
Izsvák, Z., Stüwe, E. E., Fiedler, D., Katzer, A., Jeggo, P. A., & Ivics, Z. (2004) · Molecular Cell · doi:10.1016/s1097-2765(03)00524-0 · Cited by 119
Thacker, J., Chalk, J., Ganesh, A. N., & North, P. S. (1992) · Nucleic Acids Research · doi:10.1093/nar/20.23.6183 · Cited by 117
Lavie, L., Maldener, E., Brouha, B., Meese, E. U., & Mayer, J. M. (2004) · Genome Research · doi:10.1101/gr.2745804 · Cited by 113
Burke, W. D., Malik, H. S., Jones, J. P., & Eickbush, T. H. (1999) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a026132 · Cited by 111
Rejoining of DNA double‐strand breaks in vitro by single‐strand annealing
Göttlich, B., Reichenberger, S., Feldmann, E., & Pfeiffer, P. (1998) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.1998.2580387.x · Cited by 103
Dispersal process associated with the L1 family of interspersed repetitive DNA sequences
Voliva, C. F., Martin, S. L., Hutchison, C. A., & Edgell, M. H. (1984) · Journal of Molecular Biology · doi:10.1016/0022-2836(84)90312-7 · Cited by 99
Dombroski, B. A., Feng, Q., Mathias, S. L., Sassaman, D. M., Scott, A. F., Kazazian, H. H., & Boeke, J. D. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.7.4485 · Cited by 97
Retrotransposon R1Bm endonuclease cleaves the target sequence
Feng, Q., Schumann, G. G., & Boeke, J. D. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.5.2083 · Cited by 96
Self-citationBibiłło, A., & Eickbush, T. H. (2002) · Journal of Molecular Biology · doi:10.1006/jmbi.2001.5369 · Cited by 91
End-to-End Template Jumping by the Reverse Transcriptase Encoded by the R2 Retrotransposon
Bibiłło, A., & Eickbush, T. H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m310450200 · Cited by 87
R2 and Related Site‐Specific Non‐Long Terminal Repeat Retrotransposons
Eickbush, T. H. (2007) · doi:10.1128/9781555817954.ch34 · Cited by 78
High Processivity of the Reverse Transcriptase from a Non-long Terminal Repeat Retrotransposon
Bibiłło, A., & Eickbush, T. H. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204345200 · Cited by 65
Yu, J., Marshall, K., Yamaguchi, M., Haber, J. E., & Weil, C. F. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.3.1351-1364.2004 · Cited by 65
The structures of mouse and human L1 elements reflect their insertion mechanism
Martin, S. L., Li, W.-L. P., Furano, A. V., & Boissinot, S. (2005) · Cytogenetic and Genome Research · doi:10.1159/000084956 · Cited by 58
Dombroski, B. A., Feng, Q., Mathias, S. L., Sassaman, D. M., Scott, A. F., Kazazian, H. H., & Boeke, J. D. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.7.4485-4492.1994 · Cited by 36
Odersky, A., Panyutin, I. V., Panyutin, I. G., Schunck, C., Feldmann, E., Goedecke, W., Neumann, R. D., Obe, G., & Pfeiffer, P. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m111304200 · Cited by 32
Fujimoto, H. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh304 · Cited by 24
Research works printed but not linked: 6
- 1994, Mol. Cell. Biol., 14, 4485
- 1985, Mol. Cell. Biol., 5, 2599
- 1988, Mol. Cell. Biol., 8, 1385
- 2002, Genome Biol., 3, 0052.0051
- http://www.ncbi.nlm.nih.gov/CBBresearch/Landsman/TSDfinder/; Online access to the TSDfinder PERL script.
- http://www.ncbi.nlm.nih.gov/genome/guide/human/; Online access to the human genome database.
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LINE-1 elements in structural variation and disease
Beck, C. R., Garcia-Perez, J. L., Badge, R. M., & Moran, J. V. (2011) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082509-141802 · Cited by 615
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Thomson, T., & Lin, H. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.24.110707.175327 · Cited by 565
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Metadata
- Authors
- Zingler, N., Willhoeft, U., Brose, H.-P., Schoder, V., Jahns, T., Hanschmann, K.-M. O., Morrish, T. A., Löwer, J., & Schumann, G. G.
- Affiliations
- Paul Ehrlich Institut (DE)
- Universität Hamburg (DE)
- University Medical Center Hamburg-Eppendorf (DE)
- University of Michigan (US)
- Venue
- Genome Research
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2005-06
- Volume
- 15
- Issue
- 6
- Pages
- 780-789
- ISSN
- 1088-9051 (ISSN-L)
- PMC
- PMC1142468
- OpenAlex
- W2041586254
- Cited by
- 111
- References
- 59
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 4 · 2023: 5 · 2022: 10 · 2021: 7 · 2020: 1 · 2019: 4 · 2017: 3 · 2016: 7 · 2015: 8 · 2014: 8 · 2013: 3 · 2012: 2
- Type
- posted content
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- other-oa
- Locations
- Genome Research (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- National Institutes of Health
- National Institute of General Medical Sciences (GM60518, R01GM060518)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genome Rearrangement Algorithms
- Keywords
- LINE-1 retrotransposons, Alu elements, microhomology-mediated end joining, non-homologous end joining, target-primed reverse transcription, retrotransposition
- MeSH terms
- Chromosomes, Human, DNA Replication, Humans, Models, Genetic, Recombination, Genetic, Sequence Homology, Nucleic Acid, Genome, Human, Mutagenesis, Insertional, Long Interspersed Nucleotide Elements, Alu Elements
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