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Absence of mutations in the highest mutability region of the p-53 gene in tumour-derived CHEF18 Chinese hamster cells
Author(s) -
Giuseppe Rainaldi,
Silvia Marchetti,
Barbara Capecchi,
Raffaella Meneveri,
Antonio Piras,
Rosanna Leuzzi
Publication year - 1998
Publication title -
mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.723
H-Index - 91
eISSN - 1464-3804
pISSN - 0267-8357
DOI - 10.1093/mutage/13.2.153
Subject(s) - chinese hamster , exon , complementary dna , microbiology and biotechnology , biology , gene , hamster , genetics , chinese hamster ovary cell , endonuclease , homology (biology) , mutation , cell culture
A series of independent tumour-derived Chinese hamster CHEF18 cell lines was analyzed for the presence of mutations in the cDNA region (exons 5-9) of the p53 gene, where the great majority of p53 mutations of human tumours accumulate. Since the gene is highly conserved among species, we used two primers designed on the basis of the human cDNA sequence to isolate the cDNA region from total RNA of Chinese hamster cells. The amplified fragments of 614 bp were digested with cleavase I endonuclease and fragment length polymorphism analysis showed that the restriction pattern of the p53 exons 5-9 region of tumour-derived cell lines was identical to that of diploid Chinese hamster CHL fibroblasts. Sequencing of the amplified fragments showed 100% homology between sequences, which demonstrated the absence of p53 mutations in the exons 5-9 cDNA region expected to have the highest mutability. Nevertheless, the antibody DO-7 recognized the presence of a stabilized p53 protein only in tumour-derived cell lines, which indicated that p53 expression correlated with transformed status.

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