Mitotic chromosome loss induced by methyl benzimidazole-2-yl-carbamate as a rapid mapping method in Saccharomyces cerevisiae.
Open Access
- 1 September 1982
- journal article
- research article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 2 (9) , 1080-1087
- https://doi.org/10.1128/mcb.2.9.1080
Abstract
Mitotic chromosome loss induced by methyl benzimidazole-2-yl-carbamate has been utilized as a rapid and simple method for assigning genes to individual chromosomes in Saccharomyces cerevisiae. This technique relied on the segregation of heterozygous markers in a diploid strain after methyl benzimidazole-2-yl-carbamate treatment due to loss of whole chromosomes. Correlations between the expression of an unmapped gene and that of a previously mapped recessive marker indicated chromosomal linkage. Depending on whether the unmapped gene and the marker were located in coupling or in repulsion, either positive or negative correlations were seen. The chromosomal location of several previously mapped genes were confirmed as a test of the method, and one previously unmapped gene, nib1, was mapped.This publication has 9 references indexed in Scilit:
- Genetic effects of methyl benzimidazole-2-yl-carbamate on Saccharomyces cerevisiae.Molecular and Cellular Biology, 1982
- Sensitivity to the Yeast Plasmid 2mu DNA is conferred by the nuclear allele nibl.Molecular and Cellular Biology, 1982
- Genetic map of Saccharomyces cerevisiae.1980
- The influence of the microtubule inhibitor, methyl benzimidazol-2-yl carbamate (MBC) on nuclear division and the cell cycle in Saccharomyces cerevisiaeJournal of Cell Science, 1980
- The Status of the Gene Map of the Human ChromosomesScience, 1977
- The use ofp-fluorophenylalanine with ‘master strains’ ofAspergillus nidulansfor assigning genes to linkage groupsGenetics Research, 1965