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Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis
K12 is a temperature-sensitive (ts) mutant cell line derived from Chinese hamster fibroblasts. When incubated at the nonpermissive temperature, K12 cells exhibit the following properties: (a) the cells cannot initiate DNA synthesis;o (b) the synthesis of cytosol thymidine kinase is suppressed; and (...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1982
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112043/ https://www.ncbi.nlm.nih.gov/pubmed/7085753 |
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collection | PubMed |
description | K12 is a temperature-sensitive (ts) mutant cell line derived from Chinese hamster fibroblasts. When incubated at the nonpermissive temperature, K12 cells exhibit the following properties: (a) the cells cannot initiate DNA synthesis;o (b) the synthesis of cytosol thymidine kinase is suppressed; and (c) the synthesis of three cellular proteins of molecular weights 94, 78, and 58 kdaltons is greatly enhanced. Here we characterize a spontaneous revertant clone, R12, derived from the K12 cells. We selected the revertant clone for its ability to grow at the nonpermissive temperature. Our results indicate that all the traits which constitute the K12 mutant phenotype are simultaneously reverted to the wild type in the revertant cell line, suggesting that the ts mutation of the K12 cells is of regulatory nature and exerts multiple effects on the expressed phenotypes. |
format | Text |
id | pubmed-2112043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1982 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21120432008-05-01 Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis J Cell Biol Articles K12 is a temperature-sensitive (ts) mutant cell line derived from Chinese hamster fibroblasts. When incubated at the nonpermissive temperature, K12 cells exhibit the following properties: (a) the cells cannot initiate DNA synthesis;o (b) the synthesis of cytosol thymidine kinase is suppressed; and (c) the synthesis of three cellular proteins of molecular weights 94, 78, and 58 kdaltons is greatly enhanced. Here we characterize a spontaneous revertant clone, R12, derived from the K12 cells. We selected the revertant clone for its ability to grow at the nonpermissive temperature. Our results indicate that all the traits which constitute the K12 mutant phenotype are simultaneously reverted to the wild type in the revertant cell line, suggesting that the ts mutation of the K12 cells is of regulatory nature and exerts multiple effects on the expressed phenotypes. The Rockefeller University Press 1982-03-01 /pmc/articles/PMC2112043/ /pubmed/7085753 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis |
title | Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis |
title_full | Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis |
title_fullStr | Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis |
title_full_unstemmed | Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis |
title_short | Characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis |
title_sort | characterization of a cell cycle mutant derived from hamster fibroblast: reversion analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112043/ https://www.ncbi.nlm.nih.gov/pubmed/7085753 |