Crossref
journal-article
Springer Science and Business Media LLC
Nature Genetics (297)
References
30
Referenced
375
-
Luan, D.D., Korman, M.H., Jakubczak, J.L. & Eickbush, T.H. Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: a mechanism for non-LTR retrotransposition. Cell 72, 595–605 (1993).
(
10.1016/0092-8674(93)90078-5
) / Cell by DD Luan (1993) -
Moran, J.V. & Gilbert, N. Mammalian LINE-1 retrotransposons and related elements. in Mobile DNA II (eds Craig, N., Craggie, R., Gellert, M. & Lambowitz, A.) 836–869 (ASM, Washington DC, 2002).
(
10.1128/9781555817954.ch35
) / Mobile DNA II by JV Moran (2002) -
Feng, Q., Moran, J.V., Kazazian Jr, H.H. & Boeke, J.D. Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition. Cell 87, 905–916 (1996).
(
10.1016/S0092-8674(00)81997-2
) / Cell by Q Feng (1996) -
Moran, J.V. et al. High frequency retrotransposition in cultured mammalian cells. Cell 87, 917–927 (1996).
(
10.1016/S0092-8674(00)81998-4
) / Cell by JV Moran (1996) -
Wei, W., Morrish, T.A., Alisch, R.S. & Moran, J.V. A transient assay reveals that cultured human cells can accommodate multiple LINE-1 retrotransposition events. Anal. Biochem. 284, 435–438 (2000).
(
10.1006/abio.2000.4675
) / Anal. Biochem. by W Wei (2000) -
Sassaman, D.M. et al. Many human L1 elements are capable of retrotransposition. Nature Genet. 16, 37–43 (1997).
(
10.1038/ng0597-37
) / Nature Genet. by DM Sassaman (1997) -
Wei, W. et al. Human L1 retrotransposition: cis preference versus trans complementation. Mol. Cell. Biol. 21, 1429–1439 (2001).
(
10.1128/MCB.21.4.1429-1439.2001
) / Mol. Cell. Biol. by W Wei (2001) -
Voliva, C.F., Martin, S.L., Hutchison, C.A.D. & Edgell, M.H. Dispersal process associated with the L1 family of interspersed repetitive DNA sequences. J. Mol. Biol. 178, 795–813 (1984).
(
10.1016/0022-2836(84)90312-7
) / J. Mol. Biol. by CF Voliva (1984) -
Teng, S.C., Kim, B. & Gabriel, A. Retrotransposon reverse-transcriptase-mediated repair of chromosomal breaks. Nature 383, 641–644 (1996).
(
10.1038/383641a0
) / Nature by SC Teng (1996) -
Li, Z. et al. The XRCC4 gene encodes a novel protein involved in DNA double-strand break repair and V(D)J recombination. Cell 83, 1079–1089 (1995).
(
10.1016/0092-8674(95)90135-3
) / Cell by Z Li (1995) -
Blunt, T. et al. Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation. Cell 80, 813–823 (1995).
(
10.1016/0092-8674(95)90360-7
) / Cell by T Blunt (1995) - Giaccia, A.J. et al. Human chromosome 5 complements the DNA double-strand break-repair deficiency and γ-ray sensitivity of the XR-1 hamster variant. Am. J. Hum. Genet. 47, 459–469 (1990). / Am. J. Hum. Genet. by AJ Giaccia (1990)
-
Kojima, T., Nakajima, K. & Mikoshiba, K. The disabled 1 gene is disrupted by a replacement with L1 fragment in yotari mice. Mol. Brain Res. 75, 121–127 (2000).
(
10.1016/S0169-328X(99)00313-7
) / Mol. Brain Res. by T Kojima (2000) -
Mager, D., Henthorn, P. & Smithies, O. A Chinese G γ + (A γ Δ β) zero thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints. Nucleic Acids Res. 13, 6559–6575 (1985).
(
10.1093/nar/13.18.6559
) / Nucleic Acids Res. by D Mager (1985) -
Priestley, A. et al. Molecular and biochemical characterisation of DNA-dependent protein kinase-defective rodent mutant irs-20. Nucleic Acids Res. 26, 1965–1973 (1998).
(
10.1093/nar/26.8.1965
) / Nucleic Acids Res. by A Priestley (1998) -
Luan, D.D. & Eickbush, T.H. RNA template requirements for target DNA-primed reverse transcription by the R2 retrotransposable element. Mol. Cell. Biol. 15, 3882–3891 (1995).
(
10.1128/MCB.15.7.3882
) / Mol. Cell. Biol. by DD Luan (1995) - Chambeyron, S., Bucheton, A. & Busseau, I. Tandem UAA repeats at the 3′ end of the transcript are essential for precise initiation of reverse transcription of the I factor in Drosophila melanogaster. J. Biol. Chem. online publication 6 March 2002 (DOI: 10.1074/bc.M200996200).
-
Ovchinnikov, I., Troxel, A.B. & Swergold, G.D. Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion. Genome Res. 11, 2050–2058 (2001).
(
10.1101/gr.194701
) / Genome Res. by I Ovchinnikov (2001) -
Levin, H.L. It's prime time for reverse transcriptase. Cell 88, 5–8 (1997).
(
10.1016/S0092-8674(00)81851-6
) / Cell by HL Levin (1997) -
Pardue, M.L., Danilevskaya, O.N., Traverse, K.L. & Lowenhaupt, K. Evolutionary links between telomeres and transposable elements. Genetica 100, 73–84 (1997).
(
10.1023/A:1018352706024
) / Genetica by ML Pardue (1997) -
Higashiyama, T., Noutoshi, Y., Fujie, M. & Yamada, T. Zepp, a LINE-like retrotransposon accumulated in the Chlorella telomeric region. EMBO J. 16, 3715–3723 (1997).
(
10.1093/emboj/16.12.3715
) / EMBO J. by T Higashiyama (1997) -
Stamato, T.D., Weinstein, R., Giaccia, A. & Mackenzie, L. Isolation of cell cycle-dependent γ ray-sensitive Chinese hamster ovary cell. Somat. Cell Genet. 9, 165–173 (1983).
(
10.1007/BF01543175
) / Somat. Cell Genet. by TD Stamato (1983) - Fuller, L.F. & Painter, R.B. A Chinese hamster ovary cell line hypersensitive to ionizing radiation and deficient in repair replication. Mutat. Res. 193, 109–121 (1988). / Mutat. Res. by LF Fuller (1988)
-
Stoneking, M. et al. Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa. Genome Res. 7, 1061–1071 (1997).
(
10.1101/gr.7.11.1061
) / Genome Res. by M Stoneking (1997) -
Li, J. et al. Leukaemia disease genes: large-scale cloning and pathway predictions. Nature Genet. 23, 348–353 (1999).
(
10.1038/15531
) / Nature Genet. by J Li (1999) -
Carroll, M.L. et al. Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversity. J. Mol. Biol. 311, 17–40 (2001).
(
10.1006/jmbi.2001.4847
) / J. Mol. Biol. by ML Carroll (2001) -
Dombroski, B.A., Mathias, S.L., Nanthakumar, E., Scott, A.F. & Kazazian Jr, H.H. Isolation of an active human transposable element. Science 254, 1805–1808 (1991).
(
10.1126/science.1662412
) / Science by BA Dombroski (1991) -
Narita, N. et al. Insertion of a 5′ truncated L1 element into the 3′ end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy. J. Clin. Invest. 91, 1862–1867 (1993).
(
10.1172/JCI116402
) / J. Clin. Invest. by N Narita (1993) -
Kondo-Iida, E. et al. Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD). Hum. Mol. Genet. 8, 2303–2309 (1999).
(
10.1093/hmg/8.12.2303
) / Hum. Mol. Genet. by E Kondo-Iida (1999) -
Cost, G.J. & Boeke, J.D. Targeting of human retrotransposon integration is directed by the specificity of the L1 endonuclease for regions of unusual DNA structure. Biochemistry 37, 18081–18093 (1998).
(
10.1021/bi981858s
) / Biochemistry by GJ Cost (1998)
Dates
Type | When |
---|---|
Created | 23 years, 1 month ago (July 26, 2002, 4:57 a.m.) |
Deposited | 2 years, 3 months ago (May 18, 2023, 6:17 p.m.) |
Indexed | 1 day, 12 hours ago (Sept. 3, 2025, 6:30 a.m.) |
Issued | 23 years, 3 months ago (May 13, 2002) |
Published | 23 years, 3 months ago (May 13, 2002) |
Published Online | 23 years, 3 months ago (May 13, 2002) |
Published Print | 23 years, 3 months ago (June 1, 2002) |
@article{Morrish_2002, title={DNA repair mediated by endonuclease-independent LINE-1 retrotransposition}, volume={31}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/ng898}, DOI={10.1038/ng898}, number={2}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Morrish, Tammy A. and Gilbert, Nicolas and Myers, Jeremy S. and Vincent, Bethaney J. and Stamato, Thomas D. and Taccioli, Guillermo E. and Batzer, Mark A. and Moran, John V.}, year={2002}, month=may, pages={159–165} }