Cariello N F, Cui L, Beroud C, Soussi T
Environmental Sciences and Engineering Department, University of North Carolina, Chapel Hill 27599.
Cancer Res. 1994 Aug 15;54(16):4454-60.
Mutations of the human p53 gene are of importance in the development of cancer. Perhaps 50% of all human cancers contain a mutation in the p53 oncogene and many laboratories are investigating mutations at this locus. In an effort to centralize and standardize the information regarding human p53 mutations, we have created a computerized database that contains information about DNA sequence alterations for > 3000 p53 mutants. Information on the cancer type, the origin of the cells, the specific mutation, the amino acid change, the literature citation, and other data are provided for each mutant. We have also produced a software package for the analysis of the p53 database. Routines have been developed for the analysis of single-base substitutions, including programs to (a) determine whether two mutational spectra are different, (b) display the number of mutations and mutable sites in each exon, (c) determine whether mutations show a DNA strand bias, (d) determine the frequency of transitions and transversions, (e) display the number and kind of mutations observed at each base in the coding region, (f) perform nearest neighbor analysis, and (g) display mutable amino acids in the p53 protein. The software runs only on IBM-compatible machines with MS-DOS. The software and p53 database are freely available via the Internet, using the remote file transfer protocol. These programs simplify the analysis of the rapidly increasing body of information about p53 mutations. The programs permit facile comparison between different p53 data sets, as well as the identification of mutational patterns that may be of importance to experimenters studying the mechanisms of mutation and the etiology of cancers.
人类p53基因的突变在癌症发展过程中具有重要意义。或许所有人类癌症中有50%都含有p53癌基因的突变,许多实验室都在研究该位点的突变。为了集中并规范有关人类p53突变的信息,我们创建了一个计算机化数据库,其中包含3000多个p53突变体的DNA序列改变信息。为每个突变体提供了癌症类型、细胞来源、特定突变、氨基酸变化、文献引用及其他数据。我们还开发了一个用于分析p53数据库的软件包。已开发出用于分析单碱基替换的程序,包括用于(a)确定两个突变谱是否不同的程序,(b)显示每个外显子中突变和可突变位点数量的程序,(c)确定突变是否显示DNA链偏向性的程序,(d)确定转换和颠换频率的程序,(e)显示编码区每个碱基处观察到的突变数量和类型的程序,(f)进行最近邻分析的程序,以及(g)显示p53蛋白中可突变氨基酸的程序。该软件仅在装有MS-DOS的IBM兼容机器上运行。该软件和p53数据库可通过互联网使用远程文件传输协议免费获取。这些程序简化了对迅速增加的有关p53突变信息的分析。这些程序便于不同p53数据集之间的比较,以及识别对于研究突变机制和癌症病因的实验人员可能具有重要意义的突变模式。