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Richardson, C., & Jasin, M. (2000). Frequent chromosomal translocations induced by DNA double-strand breaks. Nature, 405(6787), 697–700.

Authors 2
  1. Christine Richardson (first)
  2. Maria Jasin (additional)
References 29 Referenced 384
  1. Rabbitts, T. H. Chromosomal translocations in human cancer. Nature 372, 143–149 (1994). (10.1038/372143a0) / Nature by TH Rabbitts (1994)
  2. Mitelman, F., Mertens, F. & Johansson, B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nature Genet. 15, 417–474 (1997). (10.1038/ng0497supp-417) / Nature Genet. by F Mitelman (1997)
  3. Tycko, B. & Sklar, J. Chromosomal translocations in lymphoid neoplasia: a reappraisal of the recombinase model. Cancer Cells 2, 1–8 (1990). / Cancer Cells by B Tycko (1990)
  4. Lewis, S. M. The mechanism of V(D)J joining: lessons from molecular, immunological and comparative analyses. Adv. Immunol. 56, 27–149 (1994). (10.1016/S0065-2776(08)60450-2) / Adv. Immunol. by SM Lewis (1994)
  5. Hiom, K., Melek, M. & Gellert, M. DNA transposition by the RAG1 and RAG2 proteins: a possible source of oncogenic translocations. Cell 94, 463–470 (1998). (10.1016/S0092-8674(00)81587-1) / Cell by K Hiom (1998)
  6. Cornforth, M. N. & Bedford, J. S. Ionizing radiation damage and its early development in chromosomes. Adv. Radiat. Biol. 17, 423–496 (1993). (10.1016/B978-0-12-035417-7.50010-6) / Adv. Radiat. Biol. by MN Cornforth (1993)
  7. Ikeda, H. DNA topoisomerase-mediated illegitimate recombination. Adv. Pharmacol. 29A, 147–165 (1994). (10.1016/S1054-3589(08)60544-X) / Adv. Pharmacol. by H Ikeda (1994)
  8. Wang, P., Zhou, R., Zou, Y., Jackson-Cook, C. & Povirk, L. Highly conservative reciprocal translocations formed by apparent joining of exchanged DNA double-strand break ends. Proc. Natl Acad. Sci. USA 94, 12018–12023 (1997). (10.1073/pnas.94.22.12018) / Proc. Natl Acad. Sci. USA by P Wang (1997)
  9. Rouet, P., Smih, F. & Jasin, M. Introduction of double-strand breaks into the genome of mouse cells by expression of a rare-cutting endonuclease. Mol. Cell. Biol. 14, 8096–8106 (1994). (10.1128/MCB.14.12.8096) / Mol. Cell. Biol. by P Rouet (1994)
  10. Sargent, R. G., Brenneman, M. A. & Wilson, J. H. Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination. Mol. Cell. Biol. 17, 267–277 (1997). (10.1128/MCB.17.1.267) / Mol. Cell. Biol. by RG Sargent (1997)
  11. Liang, F., Han, M., Romanienko, P. J. & Jasin, M. Homology-directed repair is a major double-strand break repair pathway in mammalian cells. Proc. Nat. Acad. Sci. USA 95, 5172–5177 (1998). (10.1073/pnas.95.9.5172) / Proc. Nat. Acad. Sci. USA by F Liang (1998)
  12. Kadyk, L. C. & Hartwell, L. H. Sister chromatids are preferred over homologs as substrates for recombinational repair in Saccharomyces cerevisiae. Genetics 132, 387–402 (1992). (10.1093/genetics/132.2.387) / Genetics by LC Kadyk (1992)
  13. Johnson, R. D., Liu, N. & Jasin, M. Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination. Nature 401, 397–399 (1999). / Nature by RD Johnson (1999)
  14. Lin, F. L., Sperle, K. & Sternberg, N. Model for homologous recombination during transfer of DNA into mouse L cells: role for DNA ends in the recombination process. Mol. Cell. Biol. 4, 1020–1034 (1984). (10.1128/MCB.4.6.1020) / Mol. Cell. Biol. by FL Lin (1984)
  15. Jeggo, P. A. DNA breakage and repair. Adv. Genet. 38, 185–218 (1998). (10.1016/S0065-2660(08)60144-3) / Adv. Genet. by PA Jeggo (1998)
  16. Cooper, D. N., Krawczak, M. & Antonarkis, S. E. in The Genetic Basis of Human Cancer (eds Vogelstein, B. & Kinzler, K. W.) 65–94 (McGraw-Hill, New York, 1998). / The Genetic Basis of Human Cancer by DN Cooper (1998)
  17. Richardson, C., Moynahan, M. E. & Jasin, M. Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations. Genes Dev. 12, 3831–3842 (1998). (10.1101/gad.12.24.3831) / Genes Dev. by C Richardson (1998)
  18. Haber, J. E. & Leung, W. Y. Lack of chromosome territoriality in yeast: promiscuous rejoining of broken chromosome ends. Proc. Natl Acad. Sci. USA 93, 13949–13954 (1996). (10.1073/pnas.93.24.13949) / Proc. Natl Acad. Sci. USA by JE Haber (1996)
  19. Chen, C. & Kolodner, R. D. Gross chromosomal rearrangements in Saccharomyces cerevisiae replication and recombination defective mutants. Nature Genet. 23, 8–85 (1999). / Nature Genet. by C Chen (1999)
  20. Gillert, E. et al. A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells. Oncogene 18, 4663–4671 (1999). (10.1038/sj.onc.1202842) / Oncogene by E Gillert (1999)
  21. Colleaux, L., d’Auriol, L., Gailbert, F. & Dujon, B. Recognition and cleavage site of the intron-encoded omega transposase. Proc. Natl Acad. Sci. 85, 6022–6026 (1988). (10.1073/pnas.85.16.6022) / Proc. Natl Acad. Sci. by L Colleaux (1988)
  22. Jasin, M. Genetic manipulation of genomes with rare-cutting endonucleases. Trends Genet. 12, 224–228 (1996). (10.1016/0168-9525(96)10019-6) / Trends Genet. by M Jasin (1996)
  23. Beumer, K. J., Pimpinelli, S. & Golic, K. G. Induced chromosomal exchange directs the segregation of recombinant chromatids in mitosis of Drosophila. Genetics 150, 173–188 (1998). (10.1093/genetics/150.1.173) / Genetics by KJ Beumer (1998)
  24. Strout, M. P., Marcucci, G., Bloomfield, C. D. & Caligiuri, M. A. The partial tandem duplication of ALL1 (MLL) is consistently generated by Alu-mediated homologous recombination in acute myeloid leukemia. Proc. Natl Acad. Sci. USA 95, 2390–2395 (1998). (10.1073/pnas.95.5.2390) / Proc. Natl Acad. Sci. USA by MP Strout (1998)
  25. Andreasson, P. et al. Molecular characterization of jumping translocations reveals spatial and temporal breakpoint heterogeneity. Leukemia 12, 1411–1416 (1998). (10.1038/sj.leu.2401108) / Leukemia by P Andreasson (1998)
  26. Xu, X. et al. Centrosome amplification and a defective G2-M cell cycle checkpoint induce genetic instability in BRCA1 exon 11 isoform-deficient cells. Mol. Cell 3, 389–395 (1999). (10.1016/S1097-2765(00)80466-9) / Mol. Cell by X Xu (1999)
  27. Coleman, A. E., Kovalchuk, A. L., Janz, S., Palini, A. & Ried, T. Jumping translocation breakpoint regions lead to amplification of rearranged myc. Blood 93, 4442–4444 (1999). (10.1182/blood.V93.12.4442) / Blood by AE Coleman (1999)
  28. Moynahan, M. E., Chiu, J. W., Koller, B. H. & Jasin, M. Brca1 controls homology-directed repair. Mol. Cell 4, 511–518 (1999). (10.1016/S1097-2765(00)80202-6) / Mol. Cell by ME Moynahan (1999)
  29. Moynahan, M. E. & Jasin, M. Loss of heterozygosity induced by a chromosomal double-strand break. Proc. Natl Acad. Sci. USA 94, 8988–8993 (1997). (10.1073/pnas.94.17.8988) / Proc. Natl Acad. Sci. USA by ME Moynahan (1997)
Dates
Type When
Created 23 years, 1 month ago (July 26, 2002, 4:45 a.m.)
Deposited 2 years, 3 months ago (May 16, 2023, 9:58 p.m.)
Indexed 3 weeks ago (Aug. 6, 2025, 8:25 a.m.)
Issued 25 years, 2 months ago (June 1, 2000)
Published 25 years, 2 months ago (June 1, 2000)
Published Print 25 years, 2 months ago (June 1, 2000)
Funders 0

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@article{Richardson_2000, title={Frequent chromosomal translocations induced by DNA double-strand breaks}, volume={405}, ISSN={1476-4687}, url={http://dx.doi.org/10.1038/35015097}, DOI={10.1038/35015097}, number={6787}, journal={Nature}, publisher={Springer Science and Business Media LLC}, author={Richardson, Christine and Jasin, Maria}, year={2000}, month=jun, pages={697–700} }