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Genetic Complementation of the Immortal Phenotype in Group D Cell Lines by Introduction of Chromosome 7
Authors:Toshihiko Ogata  Mitsuo Oshimura  Masayoshi Namba  Michihiko Fujii  Michio Oishi  Dai Ayusawa
Affiliation:Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113;Department of Molecular and Cell Genetics, School of Life Sciences, Tottori University, 86 Nishi-cho, Yonago, Tottori-ken 683;Institute of Molecular and Cellular Biology, Okayama University Medical School, 2-5-1 Sikata-cho, Okayama, Okayama-ken 700
Abstract:Human immortal cell lines have been classified into at least four (A–D) genetic complementation groups by cell-cell hybrid analysis, i.e., a hybrid derived from different groups becomes mortal. Recently we have demonstrated that introduction of human chromosome 7 suppresses indefinite division potential in the non-tumorigenic human immortalized fibroblast lines KMST-6 and SUSM-1, both assigned to complementation group D. By extending our microcell-mediated chromosome transfer, we found that chromosome 7 also suppresses division potential in the human hepatoma line HepG2 (again, assigned to group D). Chromosome 7 was thus shown to suppress indefinite growth in the above group D cell lines irrespective of their cell types, or whether they are tumorigenic or not. Since chromosome 7 had no such effect on representative cell lines derived from complementation group A, B or C, these results indicate that the senescence gene(s) commonly mutated in the group D cell lines is located on chromosome 7.
Keywords:Cellular senescence    Immortalization    Complementation group    Chromosome transfer
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