Skip to main content
Genetics logoLink to Genetics
. 1977 Apr;85(4):573–585. doi: 10.1093/genetics/85.4.573

Association of Chromosome Loss with Centromere-Adjacent Mitotic Recombination in a Yeast Disomic Haploid

D A Campbell 1, S Fogel 1
PMCID: PMC1213642  PMID: 324869

Abstract

Experiments designed to characterize the association between disomic chromosome loss and centromere-adjacent mitotic recombination were performed. Mitotic gene convertants were selected at two heteroallelic sites on the left arm of disomic chromosome III and tested for coincident chromosome loss. The principal results are: (1) Disomic chromosome loss is markedly enhanced (nearly 40-fold) over basal levels among mitotic gene convertants selected to arise close to the centromere; no such enhancement is observed among convertants selected to arise relatively far from the centromere. (2) Chromosome loss is primarily associated with proximal allele conversion at the centromere-adjacent site, and many of these convertants are reciprocally recombined in the adjacent proximal interval. (3) Partial aneuploid exceptions provisionally identified as carrying left arm telocentrics have been found. A testable model is proposed suggesting that centromere involvement in genetic recombination may precipitate segregational disfunction leading to mitotic chromosome loss.

Full Text

The Full Text of this article is available as a PDF (819.5 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Byers B., Goetsch L. Electron microscopic observations on the meiotic karyotype of diploid and tetraploid Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1975 Dec;72(12):5056–5060. doi: 10.1073/pnas.72.12.5056. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Campbell D. A., Fogel S., Lusnak K. Mitotic chromosome loss in a disomic haploid of Saccharomyces cerevisiae. Genetics. 1975 Mar;79(3):383–396. doi: 10.1093/genetics/79.3.383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. HURST D. D., FOGEL S. MITOTIC RECOMBINATION AND HETEROALLELIC REPAIR IN SACCHAROMYCES CEREVISIAE. Genetics. 1964 Sep;50:435–458. doi: 10.1093/genetics/50.3.435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 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]
  5. Meselson M. Formation of hybrid DNA by rotary diffusion during genetic recombination. J Mol Biol. 1972 Nov 28;71(3):795–798. doi: 10.1016/s0022-2836(72)80040-8. [DOI] [PubMed] [Google Scholar]
  6. Petes T. D., Newlon C. S., Byers B., Fangman W. L. Yeast chromosomal DNA: size, structure, and replication. Cold Spring Harb Symp Quant Biol. 1974;38:9–16. doi: 10.1101/sqb.1974.038.01.004. [DOI] [PubMed] [Google Scholar]
  7. Sigal N., Alberts B. Genetic recombination: the nature of a crossed strand-exchange between two homologous DNA molecules. J Mol Biol. 1972 Nov 28;71(3):789–793. doi: 10.1016/s0022-2836(72)80039-1. [DOI] [PubMed] [Google Scholar]
  8. Steinitz-Sears L. M. Somatic instability of telocentric chromosomes in wheat and the nature of the centromere. Genetics. 1966 Jul;54(1):241–248. doi: 10.1093/genetics/54.1.241. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES