Serveur d'exploration Hippolyte Bernheim

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In situ analysis of trifluorothymidine-resistant (TFTr) mutants of L5178Y/TK+/− mouse lymphoma cells

Identifieur interne : 000C26 ( Main/Exploration ); précédent : 000C25; suivant : 000C27

In situ analysis of trifluorothymidine-resistant (TFTr) mutants of L5178Y/TK+/− mouse lymphoma cells

Auteurs : Martha M. Moore [États-Unis] ; Donald Clive [États-Unis] ; Barry E. Howard [États-Unis] ; A. Gail Batson [États-Unis] ; Nancy T. Turner [États-Unis]

Source :

RBID : ISTEX:2E7EF1B4E664C33547F75BE2E4FAE9E87AD3386E

English descriptors

Abstract

Abstract: TFTr mutants of L5178Y/TK+/− mouse lymphoma cells are analyzed as they appear in situ following cloning and incubation for 9–11 days in soft agar cloning medium. These TFTr mutants can be divided by colony size into σ, small colony, and λ, large colony, mutants. The use of a size discriminator on an automatic colony counter allows the production of histograms to evaluate the size distribution of colonies on a plate. The evaluation of these size distribution curves provides insight into the properties of σ and λ mutants. From these analyses several conclusions may be drawn. The σ phenotype is preferentially associated with the TFTr subpopulation of a treated culture. The σ phenotype is not an artifact of delayed toxicity following treatment. The frequency of quantifiable σ mutants is not affected by agar concentrations between 0.20% and 0.45% in the cloning medium. TFTr σ mutants are produced spontaneously and can be induced by a variety of mutagens. The decline in overall detectable mutant frequency observed for some mutagens with increasing time after treatment is due to the decline in σ mutant frequency. The quantitation of both σ and λ mutants is thus useful in obtaining maximum utility of the information provided by the L5178Y/TK+/− mouse lymphoma assay.

Url:
DOI: 10.1016/0027-5107(85)90193-9


Affiliations:


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<div type="abstract" xml:lang="en">Abstract: TFTr mutants of L5178Y/TK+/− mouse lymphoma cells are analyzed as they appear in situ following cloning and incubation for 9–11 days in soft agar cloning medium. These TFTr mutants can be divided by colony size into σ, small colony, and λ, large colony, mutants. The use of a size discriminator on an automatic colony counter allows the production of histograms to evaluate the size distribution of colonies on a plate. The evaluation of these size distribution curves provides insight into the properties of σ and λ mutants. From these analyses several conclusions may be drawn. The σ phenotype is preferentially associated with the TFTr subpopulation of a treated culture. The σ phenotype is not an artifact of delayed toxicity following treatment. The frequency of quantifiable σ mutants is not affected by agar concentrations between 0.20% and 0.45% in the cloning medium. TFTr σ mutants are produced spontaneously and can be induced by a variety of mutagens. The decline in overall detectable mutant frequency observed for some mutagens with increasing time after treatment is due to the decline in σ mutant frequency. The quantitation of both σ and λ mutants is thus useful in obtaining maximum utility of the information provided by the L5178Y/TK+/− mouse lymphoma assay.</div>
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