A Mouse Erythroleukemia Cell Line Possessing Friend Spleen Focus‐forming Virus gp55 Transgene and Temperature‐sensitive Mutant p53 Gene
Autor: | Mitsuaki A. Yoshida, Hisato Senda, Tatsuro Ikeuchi, Xin Xu, Yasuko Yamamura, Mariko Nagayoshi, Teruyo Tsukada, Yoji Ikawa |
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Jazyk: | angličtina |
Rok vydání: | 1995 |
Předmět: |
Cancer Research
Friend leukemia Tumor suppressor gene Transgene Molecular Sequence Data Mice Transgenic Biology Article Exon Mice Viral Envelope Proteins Gene expression Tumor Cells Cultured Animals Point Mutation Friend spleen focus‐forming virus (F‐SFFV) gp55 gene Gene Spleen Focus-Forming Viruses Base Sequence Temperature Sequence Analysis DNA Temperature-sensitive mutant Genes p53 Molecular biology Erythrodifferentiation Mice Inbred C57BL Oncology Cell culture Karyotyping Mutation Cancer research Murine erythroleukemia Temperature‐sensitive p53 mutant Leukemia Erythroblastic Acute |
Zdroj: | Japanese Journal of Cancer Research : Gann |
ISSN: | 1876-4673 0910-5050 |
Popis: | Two different erythroleukemia cell lines have been established from the splenic lesions of transgenic mice possessing the Friend spleen focus-forming virus (F-SFFV) gp55 gene. One showed a near-diploid karyotype and a temperature-sensitive (ts) p53 mutation, and the other, a hyper-triploid karyotype with double p53 mutations found by single-strand conformation polymorphism (SSCP) analysis. The cell lines both retained No.11 chromosomes on which p53 genes are localized. Another p53 allele in the cell line with the ts-p53 mutation appeared intact in the SSCP analysis of the genomic exon 5. The cells with the ts-mutant p53 gene showed no apparent change with temperature shift in their growth or dimethylsulfoxide-induced differentiation, although the wild-type p53 gene on the other allele was not expressing. This ts-p53Val-135 gene made p53-deficient fibroblasts anchorage-independent at 37 degrees C but not at 32 degrees C. This non-virus-producing, mouse erythroleukemia cell line will be useful for the study of mutated p53 function during the induction of erythrodifferentiation or apoptotic change. |
Databáze: | OpenAIRE |
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