- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Schiestl, R. H.
- Articles by Hastings, P. J.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Schiestl, R. H.
- Articles by Hastings, P. J.
Genetics, Vol 119, 237-247, Copyright © 1988
INVESTIGATIONS |
Analysis of the Mechanism for Reversion of a Disrupted Gene
R. H. Schiestl, S. Igarashi and P. J. Hastings
Present address: Department of Biology, University of Rochester, Rochester, New York 14627.
A positive selection system for intrachromosomal recombination in Saccharomyces cerevisiae has been developed. This was achieved by integration of a plasmid containing an internal fragment of the HIS3 gene into its chromosomal location. This resulted in two copies of the HIS3 gene one with a terminal deletion at the 3' end and the other with a terminal deletion at the 5' end. Reversion of the gene disruption could be brought about by plasmid excision, unequal sister chromatid exchange or sister chromatid conversion. The purpose of this study was to define the mechanisms involved in reversion of the gene disruption. The frequency of plasmid excision could be determined by placing a yeast sequence bearing an origin of replication onto the plasmid that was subsequently integrated into the yeast genome. Unequal sister chromatid exchange and conversion could be distinguished by determining the nature of the reciprocal product by Southern blotting. The results indicate that reversion might occur mainly by conversion between sister chromatids. This is because the frequency of plasmid excision was about two orders of magnitude lower than the overall frequency of reversion and no reciprocal product indicative of sister chromatid exchange was found. The findings of this presentation suggest that conversion might be an important mechanism for recombination of sister chromatids and possibly for repair of damaged DNA in S or G(2).
This article has been cited by other articles:
![]() |
Z. Kirpnick-Sobol, R. Reliene, and R. H. Schiestl Carcinogenic Cr(VI) and the Nutritional Supplement Cr(III) Induce DNA Deletions in Yeast and Mice. Cancer Res., April 1, 2006; 66(7): 3480 - 3484. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. R. Read, S. J. Raynard, A. Ruksc, and M. D. Baker Gene repeat expansion and contraction by spontaneous intrachromosomal homologous recombination in mammalian cells Nucleic Acids Res., February 20, 2004; 32(3): 1184 - 1196. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Molinier, G. Ries, S. Bonhoeffer, and B. Hohn Interchromatid and Interhomolog Recombination in Arabidopsis thaliana PLANT CELL, February 1, 2004; 16(2): 342 - 352. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Galli, T. Cervelli, and R. H. Schiestl Characterization of the Hyperrecombination Phenotype of the pol3-t Mutation of Saccharomyces cerevisiae Genetics, May 1, 2003; 164(1): 65 - 79. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. J.R. Bishop and R. H. Schiestl Homologous recombination as a mechanism for genome rearrangements: environmental and genetic effects Hum. Mol. Genet., October 1, 2000; 9(16): 2427 - 2334. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Ji, E. E. Eichler, S. Schwartz, and R. D. Nicholls Structure of Chromosomal Duplicons and their Role in Mediating Human Genomic Disorders Genome Res., May 1, 2000; 10(5): 597 - 610. [Abstract] [Full Text] |
||||
![]() |
A. J. R. Bishop, C. Barlow, A. J. Wynshaw-Boris, and R. H. Schiestl Atm Deficiency Causes an Increased Frequency of Intrachromosomal Homologous Recombination in Mice Cancer Res., January 1, 2000; 60(2): 395 - 399. [Abstract] [Full Text] |
||||
![]() |
J. Aubrecht, M.B. Secretan, A. J.R. Bishop, and R. H. Schiestl Involvement of p53 in X-ray induced intrachromosomal recombination in mice Carcinogenesis, December 1, 1999; 20(12): 2229 - 2236. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Carls and R. H. Schiestl Effect of ionizing radiation on transgenerational appearance of pun reversions in mice Carcinogenesis, December 1, 1999; 20(12): 2351 - 2354. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y.-T. Lai and W. Masker In Vitro Repair of Gaps in Bacteriophage T7 DNA J. Bacteriol., December 1, 1998; 180(23): 6193 - 6202. [Abstract] [Full Text] |
||||
![]() |
A. Galli and R. H. Schiestl Effects of DNA Double-Strand and Single-Strand Breaks on Intrachromosomal Recombination Events in Cell-Cycle-Arrested Yeast Cells Genetics, July 1, 1998; 149(3): 1235 - 1250. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. H. Schiestl, J. Aubrecht, F. Khogali, and N. Carls Carcinogens induce reversion of the mouse pink-eyed unstable mutation PNAS, April 29, 1997; 94(9): 4576 - 4581. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Schiestl, F Khogali, and N Carls Reversion of the mouse pink-eyed unstable mutation induced by low doses of x-rays Science, December 2, 1994; 266(5190): 1573 - 1576. [Abstract] [PDF] |
||||









