Miller C, Mohandas T, Wolf D, Prokocimer M, Rotter V, Koeffler H P
Nature. 1986;319(6056):783-4. doi: 10.1038/319783a0.
The p53 gene codes for a nuclear protein that has an important role in normal cellular replication. The concentration of p53 protein is frequently elevated in transformed cells. Transfection studies show that the p53 gene, in collaboration with the activated ras oncogene, can transform cells. Chromosomal localization may provide a better understanding of the relationship of p53 to other human cellular genes and of its possible role in malignancies associated with specific chromosomal rearrangements. A recent study mapped the human p53 gene to the long arm of chromosome 17 (17q21-q22) using in situ chromosomal hybridization. Here, by Southern filter hybridization of DNAs from human-rodent hybrids, we have localized the p53 gene to the short arm of human chromosome 17.
p53基因编码一种核蛋白,该蛋白在正常细胞复制中起重要作用。p53蛋白的浓度在转化细胞中经常升高。转染研究表明,p53基因与激活的ras癌基因协同作用可使细胞发生转化。染色体定位可能有助于更好地理解p53与其他人类细胞基因的关系及其在与特定染色体重排相关的恶性肿瘤中的可能作用。最近一项研究通过原位染色体杂交将人类p53基因定位到17号染色体长臂(17q21-q22)。在此,我们通过对人-鼠杂种DNA进行Southern印迹杂交,将p53基因定位到人类17号染色体短臂。