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Selective and nonselective isolation of temperature‐sensitive mutants of mouse L‐cells and their characterization
Author(s) -
Thompson L. H.,
Mankovitz R.,
Baker R. M.,
Wright J. A.,
Till J. E.,
Siminovitch L.,
Whitmore G. F.
Publication year - 1971
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1040780312
Subject(s) - mutant , plating efficiency , phenotype , mutagen , isolation (microbiology) , dna , microbiology and biotechnology , dna synthesis , cell division , biology , doubling time , cell culture , population , genetics , chemistry , cell , gene , demography , sociology
Mutants of mouse L‐cells which are temperature‐sensitive for growth have been obtained by using both selective and nonselective isolation procedures on populations treated with the mutagen nitrosoguanidine. Selective isolation was carried out by utilizing a five‐day treatment with 3 H‐TdR and ara‐C as selective agents at the nonpermissive temperature. Nonselective isolation was performed by isolating 1400 clones in the absence of selective agents and then testing them for temperature‐sensitivity. From this experiment we obtained a minimum estimate of 6 × 10 −3 for the frequency of mutants in the mutagentreated population. The mutants were characterized by their plating efficiencies, growth in suspension culture, and uptake of isotopic precursors of DNA, RNA, and protein. A range in phenotypes was observed, and there appeared to be some differences between the mutants obtained by the two types of isolation procedures. In uptake experiments the most marked reductions in the rates of precursor incorporation were seen with 3 H‐TdR, rather than 3 H‐UR or 3 H‐Leu. Different mutant lines showed considerable variation in the rate of cessation of DNA synthesis as well as the time required for termination of cell division. These experiments suggest that both types of isolation procedures are feasible for obtaining temperature‐sensitive mutants having a range of phenotypes.