Yamato K, Oka T, Hiroi M, Iwahara Y, Sugito S, Tsuchida N, Miyoshi I
Department of Medicine, Kochi Medical School.
Jpn J Cancer Res. 1993 Jan;84(1):4-8. doi: 10.1111/j.1349-7006.1993.tb02775.x.
By immunoprecipitation analysis, enhanced p53 expression was detected in 3 of 4 adult T-cell leukemia (ATL) cell lines, 1 of 3 HTLV-I-infected cell lines and 1 of 5 fresh ATL samples, compared with phytohemagglutinin-stimulated peripheral blood lymphocytes. Among these 5 high expressers, p53 missense mutations were indicated in 2 ATL cell lines and 1 fresh ATL sample by extensive p53 cDNA and genomic DNA polymerase chain reaction single-strand conformation polymorphism analysis. No mutation was found throughout the entire coding region of the remaining 2 high expressers (1 ATL and 1 HTLV-I-infected cell lines) and low expressers of p53 (2 HTLV-I-infected cell lines). Tax oncoprotein expression was found in these 2 high p53 expressers in which p53 mutation was not present, but not in low p53 expressers or cells carrying this mutation. The levels of p53 mRNA were similar among the samples regardless of p53 levels. Posttranscriptional mechanisms other than missense mutation would thus appear to increase p53 in the Tax-expressing cells but not in cells containing undetectable levels of Tax. No complex formation between p53 and Tax was observed.
通过免疫沉淀分析,与植物血凝素刺激的外周血淋巴细胞相比,在4株成人T细胞白血病(ATL)细胞系中的3株、3株HTLV-I感染细胞系中的1株以及5份新鲜ATL样本中的1份中检测到p53表达增强。在这5个高表达者中,通过广泛的p53 cDNA和基因组DNA聚合酶链反应单链构象多态性分析,在2株ATL细胞系和1份新鲜ATL样本中发现了p53错义突变。在其余2个高表达者(1株ATL和1株HTLV-I感染细胞系)以及p53低表达者(2株HTLV-I感染细胞系)的整个编码区均未发现突变。在这2个不存在p53突变的高p53表达者中发现了Tax癌蛋白表达,但在p53低表达者或携带该突变的细胞中未发现。无论p53水平如何,各样本中p53 mRNA水平相似。因此,除错义突变外的转录后机制似乎会在表达Tax的细胞中增加p53,但在Tax水平不可检测的细胞中则不会。未观察到p53与Tax之间形成复合物。