Abstract
The structural analysis of aberrant chromosomes is important for our understanding of the molecular mechanisms underlying chromosomal rearrangements. We have identified a number of diploid Saccharomyces cerevisiae clones that have undergone loss of heterozygosity (LOH) leading to functional inactivation of the hemizygous URA3 marker placed on the right arm of chromosome III. Aberrant-sized chromosomes derived from chromosome III were detected in approximately 8% of LOH clones. Here, we have analyzed the structure of the aberrant chromosomes in 45 LOH clones with a PCR-based method that determines the ploidy of a series of loci on chromosome III. The alterations included various deletions and amplifications. Sequencing of the junctions revealed that all the breakpoints had been made within repeat sequences in the yeast genome, namely, MAT-HMR, which resulted in intrachromosomal deletion, and retrotransposon Ty1 elements, which were involved in various translocations. Although the translocations involved different breakpoints on different chromosomes, all breakpoints were exclusively within Ty1 elements. Some of the resulting Ty1 elements left at the breakpoints had a complex construction that indicated the involvement of other Ty1 elements not present at the parental breakpoints. These indicate that Ty1 elements are crucially involved in the generation of chromosomal rearrangements in diploid yeast cells.
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- Breilmann D., Gafner J., Ciriacy M. Gene conversion and reciprocal exchange in a Ty-mediated translocation in yeast. Curr Genet. 1985;9(7):553–560. doi: 10.1007/BF00381167. [DOI] [PubMed] [Google Scholar]
- Chen C., Kolodner R. D. Gross chromosomal rearrangements in Saccharomyces cerevisiae replication and recombination defective mutants. Nat Genet. 1999 Sep;23(1):81–85. doi: 10.1038/12687. [DOI] [PubMed] [Google Scholar]
- Chen C., Umezu K., Kolodner R. D. Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair. Mol Cell. 1998 Jul;2(1):9–22. doi: 10.1016/s1097-2765(00)80109-4. [DOI] [PubMed] [Google Scholar]
- Christman M. F., Dietrich F. S., Fink G. R. Mitotic recombination in the rDNA of S. cerevisiae is suppressed by the combined action of DNA topoisomerases I and II. Cell. 1988 Nov 4;55(3):413–425. doi: 10.1016/0092-8674(88)90027-x. [DOI] [PubMed] [Google Scholar]
- Downs K. M., Brennan G., Liebman S. W. Deletions extending from a single Ty1 element in Saccharomyces cerevisiae. Mol Cell Biol. 1985 Dec;5(12):3451–3457. doi: 10.1128/mcb.5.12.3451. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eichelberger L., Technical Assistance of Michael Roma THE DISTRIBUTION OF WATER AND ELECTROLYTES BETWEEN BLOOD AND SKELETAL MUSCLE IN EXPERIMENTAL HYPERTENSION. J Exp Med. 1943 Mar 1;77(3):205–213. doi: 10.1084/jem.77.3.205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gupta P. K., Sahota A., Boyadjiev S. A., Bye S., Shao C., O'Neill J. P., Hunter T. C., Albertini R. J., Stambrook P. J., Tischfield J. A. High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination. Cancer Res. 1997 Mar 15;57(6):1188–1193. [PubMed] [Google Scholar]
- Hani J., Feldmann H. tRNA genes and retroelements in the yeast genome. Nucleic Acids Res. 1998 Feb 1;26(3):689–696. doi: 10.1093/nar/26.3.689. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hiraoka M., Watanabe K., Umezu K., Maki H. Spontaneous loss of heterozygosity in diploid Saccharomyces cerevisiae cells. Genetics. 2000 Dec;156(4):1531–1548. doi: 10.1093/genetics/156.4.1531. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ji H., Moore D. P., Blomberg M. A., Braiterman L. T., Voytas D. F., Natsoulis G., Boeke J. D. Hotspots for unselected Ty1 transposition events on yeast chromosome III are near tRNA genes and LTR sequences. Cell. 1993 Jun 4;73(5):1007–1018. doi: 10.1016/0092-8674(93)90278-x. [DOI] [PubMed] [Google Scholar]
- Keil R. L., McWilliams A. D. A gene with specific and global effects on recombination of sequences from tandemly repeated genes in Saccharomyces cerevisiae. Genetics. 1993 Nov;135(3):711–718. doi: 10.1093/genetics/135.3.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klein H. L. Genetic control of intrachromosomal recombination. Bioessays. 1995 Feb;17(2):147–159. doi: 10.1002/bies.950170210. [DOI] [PubMed] [Google Scholar]
- Knudson A. G. Antioncogenes and human cancer. Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):10914–10921. doi: 10.1073/pnas.90.23.10914. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kupiec M., Petes T. D. Allelic and ectopic recombination between Ty elements in yeast. Genetics. 1988 Jul;119(3):549–559. doi: 10.1093/genetics/119.3.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lasko D., Cavenee W., Nordenskjöld M. Loss of constitutional heterozygosity in human cancer. Annu Rev Genet. 1991;25:281–314. doi: 10.1146/annurev.ge.25.120191.001433. [DOI] [PubMed] [Google Scholar]
- Liebman S., Shalit P., Picologlou S. Ty elements are involved in the formation of deletions in DEL1 strains of Saccharomyces cerevisiae. Cell. 1981 Nov;26(3 Pt 1):401–409. doi: 10.1016/0092-8674(81)90209-9. [DOI] [PubMed] [Google Scholar]
- 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. 1984 Jun;4(6):1020–1034. doi: 10.1128/mcb.4.6.1020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Malkova A., Ivanov E. L., Haber J. E. Double-strand break repair in the absence of RAD51 in yeast: a possible role for break-induced DNA replication. Proc Natl Acad Sci U S A. 1996 Jul 9;93(14):7131–7136. doi: 10.1073/pnas.93.14.7131. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maryon E., Carroll D. Characterization of recombination intermediates from DNA injected into Xenopus laevis oocytes: evidence for a nonconservative mechanism of homologous recombination. Mol Cell Biol. 1991 Jun;11(6):3278–3287. doi: 10.1128/mcb.11.6.3278. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Melamed C., Nevo Y., Kupiec M. Involvement of cDNA in homologous recombination between Ty elements in Saccharomyces cerevisiae. Mol Cell Biol. 1992 Apr;12(4):1613–1620. doi: 10.1128/mcb.12.4.1613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moore J. K., Haber J. E. Capture of retrotransposon DNA at the sites of chromosomal double-strand breaks. Nature. 1996 Oct 17;383(6601):644–646. doi: 10.1038/383644a0. [DOI] [PubMed] [Google Scholar]
- Morrow D. M., Connelly C., Hieter P. "Break copy" duplication: a model for chromosome fragment formation in Saccharomyces cerevisiae. Genetics. 1997 Oct;147(2):371–382. doi: 10.1093/genetics/147.2.371. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Myung K., Datta A., Chen C., Kolodner R. D. SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination. Nat Genet. 2001 Jan;27(1):113–116. doi: 10.1038/83673. [DOI] [PubMed] [Google Scholar]
- Myung K., Datta A., Kolodner R. D. Suppression of spontaneous chromosomal rearrangements by S phase checkpoint functions in Saccharomyces cerevisiae. Cell. 2001 Feb 9;104(3):397–408. doi: 10.1016/s0092-8674(01)00227-6. [DOI] [PubMed] [Google Scholar]
- Oliver S. G., van der Aart Q. J., Agostoni-Carbone M. L., Aigle M., Alberghina L., Alexandraki D., Antoine G., Anwar R., Ballesta J. P., Benit P. The complete DNA sequence of yeast chromosome III. Nature. 1992 May 7;357(6373):38–46. doi: 10.1038/357038a0. [DOI] [PubMed] [Google Scholar]
- Point D., Rodriguez J., Ferrante B., Brugère J. Cancers du voile du palais. Résultats de la chirurgie de rattrapage. Ann Otolaryngol Chir Cervicofac. 1987;104(6):395–397. [PubMed] [Google Scholar]
- Pâques F., Haber J. E. Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae. Microbiol Mol Biol Rev. 1999 Jun;63(2):349–404. doi: 10.1128/mmbr.63.2.349-404.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rachidi N., Barre P., Blondin B. Multiple Ty-mediated chromosomal translocations lead to karyotype changes in a wine strain of Saccharomyces cerevisiae. Mol Gen Genet. 1999 Jun;261(4-5):841–850. doi: 10.1007/s004380050028. [DOI] [PubMed] [Google Scholar]
- Roeder G. S., Fink G. R. DNA rearrangements associated with a transposable element in yeast. Cell. 1980 Aug;21(1):239–249. doi: 10.1016/0092-8674(80)90131-2. [DOI] [PubMed] [Google Scholar]
- Rothstein R. Deletions of a tyrosine tRNA gene in S. cerevisiae. Cell. 1979 May;17(1):185–190. doi: 10.1016/0092-8674(79)90306-4. [DOI] [PubMed] [Google Scholar]
- Rothstein R., Helms C., Rosenberg N. Concerted deletions and inversions are caused by mitotic recombination between delta sequences in Saccharomyces cerevisiae. Mol Cell Biol. 1987 Mar;7(3):1198–1207. doi: 10.1128/mcb.7.3.1198. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sugawara N., Haber J. E. Characterization of double-strand break-induced recombination: homology requirements and single-stranded DNA formation. Mol Cell Biol. 1992 Feb;12(2):563–575. doi: 10.1128/mcb.12.2.563. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Teng S. C., Kim B., Gabriel A. Retrotransposon reverse-transcriptase-mediated repair of chromosomal breaks. Nature. 1996 Oct 17;383(6601):641–644. doi: 10.1038/383641a0. [DOI] [PubMed] [Google Scholar]
- Tischfield J. A. Loss of heterozygosity or: how I learned to stop worrying and love mitotic recombination. Am J Hum Genet. 1997 Nov;61(5):995–999. doi: 10.1086/301617. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warmington J. R., Anwar R., Newlon C. S., Waring R. B., Davies R. W., Indge K. J., Oliver S. G. A 'hot-spot' for Ty transposition on the left arm of yeast chromosome III. Nucleic Acids Res. 1986 Apr 25;14(8):3475–3485. doi: 10.1093/nar/14.8.3475. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warmington J. R., Green R. P., Newlon C. S., Oliver S. G. Polymorphisms on the right arm of yeast chromosome III associated with Ty transposition and recombination events. Nucleic Acids Res. 1987 Nov 11;15(21):8963–8982. doi: 10.1093/nar/15.21.8963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wicksteed B. L., Collins I., Dershowitz A., Stateva L. I., Green R. P., Oliver S. G., Brown A. J., Newlon C. S. A physical comparison of chromosome III in six strains of Saccharomyces cerevisiae. Yeast. 1994 Jan;10(1):39–57. doi: 10.1002/yea.320100105. [DOI] [PubMed] [Google Scholar]
- Wicksteed B. L., Collins I., Dershowitz A., Stateva L. I., Green R. P., Oliver S. G., Brown A. J., Newlon C. S. A physical comparison of chromosome III in six strains of Saccharomyces cerevisiae. Yeast. 1994 Jan;10(1):39–57. doi: 10.1002/yea.320100105. [DOI] [PubMed] [Google Scholar]