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Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae.

A number of genetic systems are described which involve the use of the yeast Saccharomyces cerevisiae. The systems may be used to detect the production of aneuploid cells produced during both mitotic and meiotic cell division in the presence of genetically active chemicals. During mitotic cell divis...

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Detalles Bibliográficos
Autores principales: Parry, J M, Sharp, D, Parry, E M
Formato: Texto
Lenguaje:English
Publicado: 1979
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637641/
https://www.ncbi.nlm.nih.gov/pubmed/387403
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author Parry, J M
Sharp, D
Parry, E M
author_facet Parry, J M
Sharp, D
Parry, E M
author_sort Parry, J M
collection PubMed
description A number of genetic systems are described which involve the use of the yeast Saccharomyces cerevisiae. The systems may be used to detect the production of aneuploid cells produced during both mitotic and meiotic cell division in the presence of genetically active chemicals. During mitotic cell division, monosomic colonies (2n - 1) may be detected by plating upon selective medium. Increases in such monosomic colonies are produced by exposure of cells to a number of chemical mutagens such as ethyl methane-sulfonate and mitomycin C. More importantly, monosomic colonies are also induced by nonmutagens such as sulfacetamide and saccharin, which suggests that such chemicals are capable of inducing aneuploidy (aneugenic) in the absence of mutagenic activity. Genetic analysis of aneuploid colonies produced on nonselective medium indicate that at least a proportion of the monosomic colonies were the result of mitotic nondisjunction. During meiotic cell division, disomic cells (n + 1) produced by chromosome nondisjunction may be detected by plating on selective media. The frequency of disomic cells has been shown to increase after exposure to p-fluorophenylalanine.
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spelling pubmed-16376412006-11-17 Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae. Parry, J M Sharp, D Parry, E M Environ Health Perspect Research Article A number of genetic systems are described which involve the use of the yeast Saccharomyces cerevisiae. The systems may be used to detect the production of aneuploid cells produced during both mitotic and meiotic cell division in the presence of genetically active chemicals. During mitotic cell division, monosomic colonies (2n - 1) may be detected by plating upon selective medium. Increases in such monosomic colonies are produced by exposure of cells to a number of chemical mutagens such as ethyl methane-sulfonate and mitomycin C. More importantly, monosomic colonies are also induced by nonmutagens such as sulfacetamide and saccharin, which suggests that such chemicals are capable of inducing aneuploidy (aneugenic) in the absence of mutagenic activity. Genetic analysis of aneuploid colonies produced on nonselective medium indicate that at least a proportion of the monosomic colonies were the result of mitotic nondisjunction. During meiotic cell division, disomic cells (n + 1) produced by chromosome nondisjunction may be detected by plating on selective media. The frequency of disomic cells has been shown to increase after exposure to p-fluorophenylalanine. 1979-08 /pmc/articles/PMC1637641/ /pubmed/387403 Text en
spellingShingle Research Article
Parry, J M
Sharp, D
Parry, E M
Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae.
title Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae.
title_full Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae.
title_fullStr Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae.
title_full_unstemmed Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae.
title_short Detection of mitotic and meiotic aneuploidy in the yeast Saccharomyces cerevisiae.
title_sort detection of mitotic and meiotic aneuploidy in the yeast saccharomyces cerevisiae.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637641/
https://www.ncbi.nlm.nih.gov/pubmed/387403
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