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. 1997 Jul;17(7):3614–3628. doi: 10.1128/mcb.17.7.3614

Fine-resolution analysis of products of intrachromosomal homeologous recombination in mammalian cells.

D Yang 1, A S Waldman 1
PMCID: PMC232214  PMID: 9199296

Abstract

Mouse Ltk- cell lines that contained a herpes simplex virus type 1 (HSV-1) thymidine kinase (tk) gene with a 16-bp insertion mutation linked to either a defective HSV-2 tk gene or a hybrid tk sequence comprised of HSV-1 and HSV-2 tk sequences were constructed. HSV-1 and HSV-2 tk genes have 81% nucleotide identity and hence are homeologous. Correction of the insertion mutant HSV-1 tk gene via recombination with the hybrid tk sequence required an exchange between homeologous tk sequences, although recombination could initiate within a region of significant sequence identity. Seven cell lines containing linked HSV-1 and HSV-1-HSV-2 hybrid tk sequences gave rise to tk+ segregants at an average rate of 10(-8) events per cell division. DNA sequencing revealed that each recombinant from these lines displayed an apparent gene conversion which involved an accurate transfer of an uninterrupted block of information between homeologous tk sequences. Conversion tract lengths ranged from 35 to >330 bp. In contrast, cell lines containing linked HSV-1 and HSV-2 tk sequences with no significant stretches of sequence identity had an overall rate of homeologous recombination of <10(-9). One such cell line produced homeologous recombinants at a rate of 10(-8). Strikingly, all homeologous recombinants from this latter cell line were due to crossovers between the HSV-1 and HSV-2 tk genes. Our results, which provide the first detailed analysis of homeologous recombination within a mammalian genome, suggest that rearrangements in mammalian genomes are regulated by the degree of sequence divergence located at the site of recombination initiation.

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Selected References

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  1. Alani E., Reenan R. A., Kolodner R. D. Interaction between mismatch repair and genetic recombination in Saccharomyces cerevisiae. Genetics. 1994 May;137(1):19–39. doi: 10.1093/genetics/137.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bailis A. M., Rothstein R. A defect in mismatch repair in Saccharomyces cerevisiae stimulates ectopic recombination between homeologous genes by an excision repair dependent process. Genetics. 1990 Nov;126(3):535–547. doi: 10.1093/genetics/126.3.535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Belmaaza A., Milot E., Villemure J. F., Chartrand P. Interference of DNA sequence divergence with precise recombinational DNA repair in mammalian cells. EMBO J. 1994 Nov 15;13(22):5355–5360. doi: 10.1002/j.1460-2075.1994.tb06870.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bollag R. J., Elwood D. R., Tobin E. D., Godwin A. R., Liskay R. M. Formation of heteroduplex DNA during mammalian intrachromosomal gene conversion. Mol Cell Biol. 1992 Apr;12(4):1546–1552. doi: 10.1128/mcb.12.4.1546. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bollag R. J., Liskay R. M. Conservative intrachromosomal recombination between inverted repeats in mouse cells: association between reciprocal exchange and gene conversion. Genetics. 1988 May;119(1):161–169. doi: 10.1093/genetics/119.1.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bollag R. J., Waldman A. S., Liskay R. M. Homologous recombination in mammalian cells. Annu Rev Genet. 1989;23:199–225. doi: 10.1146/annurev.ge.23.120189.001215. [DOI] [PubMed] [Google Scholar]
  7. Brinster R. L., Braun R. E., Lo D., Avarbock M. R., Oram F., Palmiter R. D. Targeted correction of a major histocompatibility class II E alpha gene by DNA microinjected into mouse eggs. Proc Natl Acad Sci U S A. 1989 Sep;86(18):7087–7091. doi: 10.1073/pnas.86.18.7087. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Canning S., Dryja T. P. Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene. Proc Natl Acad Sci U S A. 1989 Jul;86(13):5044–5048. doi: 10.1073/pnas.86.13.5044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Capecchi M. R. High efficiency transformation by direct microinjection of DNA into cultured mammalian cells. Cell. 1980 Nov;22(2 Pt 2):479–488. doi: 10.1016/0092-8674(80)90358-x. [DOI] [PubMed] [Google Scholar]
  10. Capizzi R. L., Jameson J. W. A table for the estimation of the spontaneous mutation rate of cells in culture. Mutat Res. 1973 Jan;17(1):147–148. doi: 10.1016/0027-5107(73)90265-0. [DOI] [PubMed] [Google Scholar]
  11. Carpenter C. D., Oh J. W., Zhang C., Simon A. E. Involvement of a stem-loop structure in the location of junction sites in viral RNA recombination. J Mol Biol. 1995 Feb 3;245(5):608–622. doi: 10.1006/jmbi.1994.0050. [DOI] [PubMed] [Google Scholar]
  12. Datta A., Adjiri A., New L., Crouse G. F., Jinks Robertson S. Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae. Mol Cell Biol. 1996 Mar;16(3):1085–1093. doi: 10.1128/mcb.16.3.1085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Desautels L., Brouillette S., Wallenburg J., Belmaaza A., Gusew N., Trudel P., Chartrand P. Characterization of nonconservative homologous junctions in mammalian cells. Mol Cell Biol. 1990 Dec;10(12):6613–6618. doi: 10.1128/mcb.10.12.6613. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ernst J. F., Stewart J. W., Sherman F. The cyc1-11 mutation in yeast reverts by recombination with a nonallelic gene: composite genes determining the iso-cytochromes c. Proc Natl Acad Sci U S A. 1981 Oct;78(10):6334–6338. doi: 10.1073/pnas.78.10.6334. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Goguel V., Delahodde A., Jacq C. Connections between RNA splicing and DNA intron mobility in yeast mitochondria: RNA maturase and DNA endonuclease switching experiments. Mol Cell Biol. 1992 Feb;12(2):696–705. doi: 10.1128/mcb.12.2.696. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Gordenin D. A., Lobachev K. S., Degtyareva N. P., Malkova A. L., Perkins E., Resnick M. A. Inverted DNA repeats: a source of eukaryotic genomic instability. Mol Cell Biol. 1993 Sep;13(9):5315–5322. doi: 10.1128/mcb.13.9.5315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Harris S., Rudnicki K. S., Haber J. E. Gene conversions and crossing over during homologous and homeologous ectopic recombination in Saccharomyces cerevisiae. Genetics. 1993 Sep;135(1):5–16. doi: 10.1093/genetics/135.1.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kit S., Kit M., Qavi H., Trkula D., Otsuka H. Nucleotide sequence of the herpes simplex virus type 2 (HSV-2) thymidine kinase gene and predicted amino acid sequence of thymidine kinase polypeptide and its comparison with the HSV-1 thymidine kinase gene. Biochim Biophys Acta. 1983 Nov 17;741(2):158–170. doi: 10.1016/0167-4781(83)90056-8. [DOI] [PubMed] [Google Scholar]
  19. Letsou A., Liskay R. M. Effect of the molecular nature of mutation on the efficiency of intrachromosomal gene conversion in mouse cells. Genetics. 1987 Dec;117(4):759–769. doi: 10.1093/genetics/117.4.759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Liskay R. M., Letsou A., Stachelek J. L. Homology requirement for efficient gene conversion between duplicated chromosomal sequences in mammalian cells. Genetics. 1987 Jan;115(1):161–167. doi: 10.1093/genetics/115.1.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Liskay R. M., Stachelek J. L. Information transfer between duplicated chromosomal sequences in mammalian cells involves contiguous regions of DNA. Proc Natl Acad Sci U S A. 1986 Mar;83(6):1802–1806. doi: 10.1073/pnas.83.6.1802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Liskay R. M., Stachelek J. L., Letsou A. Homologous recombination between repeated chromosomal sequences in mouse cells. Cold Spring Harb Symp Quant Biol. 1984;49:183–189. doi: 10.1101/sqb.1984.049.01.021. [DOI] [PubMed] [Google Scholar]
  23. Lovett S. T., Drapkin P. T., Sutera V. A., Jr, Gluckman-Peskind T. J. A sister-strand exchange mechanism for recA-independent deletion of repeated DNA sequences in Escherichia coli. Genetics. 1993 Nov;135(3):631–642. doi: 10.1093/genetics/135.3.631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Lukacsovich T., Yang D., Waldman A. S. Repair of a specific double-strand break generated within a mammalian chromosome by yeast endonuclease I-SceI. Nucleic Acids Res. 1994 Dec 25;22(25):5649–5657. doi: 10.1093/nar/22.25.5649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Luria S. E., Delbrück M. Mutations of Bacteria from Virus Sensitivity to Virus Resistance. Genetics. 1943 Nov;28(6):491–511. doi: 10.1093/genetics/28.6.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Matic I., Radman M., Rayssiguier C. Structure of recombinants from conjugational crosses between Escherichia coli donor and mismatch-repair deficient Salmonella typhimurium recipients. Genetics. 1994 Jan;136(1):17–26. doi: 10.1093/genetics/136.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Merrihew R. V., Marburger K., Pennington S. L., Roth D. B., Wilson J. H. High-frequency illegitimate integration of transfected DNA at preintegrated target sites in a mammalian genome. Mol Cell Biol. 1996 Jan;16(1):10–18. doi: 10.1128/mcb.16.1.10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Meselson M. S., Radding C. M. A general model for genetic recombination. Proc Natl Acad Sci U S A. 1975 Jan;72(1):358–361. doi: 10.1073/pnas.72.1.358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Mezard C., Nicolas A. Homologous, homeologous, and illegitimate repair of double-strand breaks during transformation of a wild-type strain and a rad52 mutant strain of Saccharomyces cerevisiae. Mol Cell Biol. 1994 Feb;14(2):1278–1292. doi: 10.1128/mcb.14.2.1278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Mézard C., Pompon D., Nicolas A. Recombination between similar but not identical DNA sequences during yeast transformation occurs within short stretches of identity. Cell. 1992 Aug 21;70(4):659–670. doi: 10.1016/0092-8674(92)90434-e. [DOI] [PubMed] [Google Scholar]
  31. Porter G., Westmoreland J., Priebe S., Resnick M. A. Homologous and homeologous intermolecular gene conversion are not differentially affected by mutations in the DNA damage or the mismatch repair genes RAD1, RAD50, RAD51, RAD52, RAD54, PMS1 and MSH2. Genetics. 1996 Jun;143(2):755–767. doi: 10.1093/genetics/143.2.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Priebe S. D., Westmoreland J., Nilsson-Tillgren T., Resnick M. A. Induction of recombination between homologous and diverged DNAs by double-strand gaps and breaks and role of mismatch repair. Mol Cell Biol. 1994 Jul;14(7):4802–4814. doi: 10.1128/mcb.14.7.4802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Radman M. Mismatch repair and the fidelity of genetic recombination. Genome. 1989;31(1):68–73. doi: 10.1139/g89-014. [DOI] [PubMed] [Google Scholar]
  34. Rayssiguier C., Dohet C., Radman M. Interspecific recombination between Escherichia coli and Salmonella typhimurium occurs by the RecABCD pathway. Biochimie. 1991 Apr;73(4):371–374. doi: 10.1016/0300-9084(91)90103-8. [DOI] [PubMed] [Google Scholar]
  35. Rayssiguier C., Thaler D. S., Radman M. The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants. Nature. 1989 Nov 23;342(6248):396–401. doi: 10.1038/342396a0. [DOI] [PubMed] [Google Scholar]
  36. Resnick M. A., Zgaga Z., Hieter P., Westmoreland J., Fogel S., Nilsson-Tillgren T. Recombinant repair of diverged DNAs: a study of homoeologous chromosomes and mammalian YACs in yeast. Mol Gen Genet. 1992 Jul;234(1):65–73. doi: 10.1007/BF00272346. [DOI] [PubMed] [Google Scholar]
  37. Rubnitz J., Subramani S. The minimum amount of homology required for homologous recombination in mammalian cells. Mol Cell Biol. 1984 Nov;4(11):2253–2258. doi: 10.1128/mcb.4.11.2253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Scheerer J. B., Adair G. M. Homology dependence of targeted recombination at the Chinese hamster APRT locus. Mol Cell Biol. 1994 Oct;14(10):6663–6673. doi: 10.1128/mcb.14.10.6663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Selva E. M., New L., Crouse G. F., Lahue R. S. Mismatch correction acts as a barrier to homeologous recombination in Saccharomyces cerevisiae. Genetics. 1995 Mar;139(3):1175–1188. doi: 10.1093/genetics/139.3.1175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Shen P., Huang H. V. Effect of base pair mismatches on recombination via the RecBCD pathway. Mol Gen Genet. 1989 Aug;218(2):358–360. doi: 10.1007/BF00331291. [DOI] [PubMed] [Google Scholar]
  41. Shen P., Huang H. V. Homologous recombination in Escherichia coli: dependence on substrate length and homology. Genetics. 1986 Mar;112(3):441–457. doi: 10.1093/genetics/112.3.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Southern P. J., Berg P. Transformation of mammalian cells to antibiotic resistance with a bacterial gene under control of the SV40 early region promoter. J Mol Appl Genet. 1982;1(4):327–341. [PubMed] [Google Scholar]
  43. Stachelek J. L., Liskay R. M. Accuracy of intrachromosomal gene conversion in mouse cells. Nucleic Acids Res. 1988 May 11;16(9):4069–4076. doi: 10.1093/nar/16.9.4069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Swain M. A., Galloway D. A. Nucleotide sequence of the herpes simplex virus type 2 thymidine kinase gene. J Virol. 1983 Jun;46(3):1045–1050. doi: 10.1128/jvi.46.3.1045-1050.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Szostak J. W., Orr-Weaver T. L., Rothstein R. J., Stahl F. W. The double-strand-break repair model for recombination. Cell. 1983 May;33(1):25–35. doi: 10.1016/0092-8674(83)90331-8. [DOI] [PubMed] [Google Scholar]
  46. Wagner M. J., Sharp J. A., Summers W. C. Nucleotide sequence of the thymidine kinase gene of herpes simplex virus type 1. Proc Natl Acad Sci U S A. 1981 Mar;78(3):1441–1445. doi: 10.1073/pnas.78.3.1441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Waldman A. S., Liskay R. M. Dependence of intrachromosomal recombination in mammalian cells on uninterrupted homology. Mol Cell Biol. 1988 Dec;8(12):5350–5357. doi: 10.1128/mcb.8.12.5350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Waldman A. S., Liskay R. M. Differential effects of base-pair mismatch on intrachromosomal versus extrachromosomal recombination in mouse cells. Proc Natl Acad Sci U S A. 1987 Aug;84(15):5340–5344. doi: 10.1073/pnas.84.15.5340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Waldman A. S., Waldman B. C. Stimulation of intrachromosomal homologous recombination in mammalian cells by an inhibitor of poly(ADP-ribosylation). Nucleic Acids Res. 1991 Nov 11;19(21):5943–5947. doi: 10.1093/nar/19.21.5943. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Wells R. D. Molecular basis of genetic instability of triplet repeats. J Biol Chem. 1996 Feb 9;271(6):2875–2878. doi: 10.1074/jbc.271.6.2875. [DOI] [PubMed] [Google Scholar]
  51. Wheeler C. J., Maloney D., Fogel S., Goodenow R. S. Microconversion between murine H-2 genes integrated into yeast. Nature. 1990 Sep 13;347(6289):192–194. doi: 10.1038/347192a0. [DOI] [PubMed] [Google Scholar]
  52. Worth L., Jr, Clark S., Radman M., Modrich P. Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs. Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):3238–3241. doi: 10.1073/pnas.91.8.3238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Yang D., Waldman A. S. An examination of the effects of double-strand breaks on extrachromosomal recombination in mammalian cells. Genetics. 1992 Dec;132(4):1081–1093. doi: 10.1093/genetics/132.4.1081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. de Wind N., Dekker M., Berns A., Radman M., te Riele H. Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer. Cell. 1995 Jul 28;82(2):321–330. doi: 10.1016/0092-8674(95)90319-4. [DOI] [PubMed] [Google Scholar]

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