Matlashewski G, Lamb P, Pim D, Peacock J, Crawford L, Benchimol S
EMBO J. 1984 Dec 20;3(13):3257-62. doi: 10.1002/j.1460-2075.1984.tb02287.x.
A cDNA clone for human p53 cellular tumor antigen has been isolated and characterized. This clone contains the complete 3'-untranslated region and most of the open reading frame for the protein. Nucleotide sequence analysis revealed that p53 mRNA contains an Alu repeat in the 3'-untranslated region. Hybridization selection experiments showed this clone was capable of selectively binding p53 mRNA. In vitro translation of SV80 mRNA resulted in the synthesis of two immunoreactive p53 polypeptide species. Northern blot analysis showed that human p53 mRNA was 2.8 kb in length and was present in cell lines containing high and low levels of p53 protein. There appears to be only a single p53 gene in human cells and Southern blot analysis demonstrated no major genomic rearrangements or amplification of the p53 gene in the transformed cell lines examined.
一个用于人类p53细胞肿瘤抗原的cDNA克隆已被分离和鉴定。该克隆包含完整的3'非翻译区和该蛋白质的大部分开放阅读框。核苷酸序列分析表明,p53 mRNA在3'非翻译区含有一个Alu重复序列。杂交筛选实验表明,该克隆能够选择性地结合p53 mRNA。SV80 mRNA的体外翻译导致合成了两种具有免疫反应性的p53多肽。Northern印迹分析表明,人类p53 mRNA长度为2.8 kb,存在于含有高水平和低水平p53蛋白的细胞系中。人类细胞中似乎只有一个p53基因,Southern印迹分析表明,在所检测的转化细胞系中,p53基因没有主要的基因组重排或扩增。