Liu Xiao-Rong, Shan Xiang-Nian, Friedl W, Uhlhaas S, Li Jin-Tian, Propping P, Wang Ya-Ping
Laboratory of Medical Genetics, Medical School, Nanjing University, Nanjing 210093, China.
Yi Chuan Xue Bao. 2005 Sep;32(9):903-8.
The protein truncation test was established for analyzing mutations in the adenomatous polyposis coli (APC) gene which plays an important role in familial adenomatous polyposis (FAP). The sites of APC mutations and the clinic features of FAP patients were examined to find the relationship between them. Genomic DNA, which was extracted from peripheral blood lymphocytes of 22 FAP patients and the normal colon tissues of 43 sporadic colorectal cancers, were examined for mutations in exon15 of the APC gene by using PCR-TNT T7 Quick Coupled Tanscription/Translation System. The subsequent sequencing was used to confirm the mutation sites. Germline mutations were found in 5 of 22 FAP patients. All of the five mutations showed base pair deletions and led to produce truncated protein. No truncating germline mutation was found in normal tissues of 43 sporadic colorectal cancers. The protein truncation test is a sensitive and accurate technique to detect truncated mutations especially in the large exons of APC gene. It can be used as an routine method for assisting the early diagnosis of the FAP patients.
蛋白质截短试验用于分析在家族性腺瘤性息肉病(FAP)中起重要作用的腺瘤性息肉病 coli(APC)基因的突变。检测 APC 突变位点和 FAP 患者的临床特征以发现它们之间的关系。使用 PCR-TNT T7 快速偶联转录/翻译系统,对从 22 例 FAP 患者外周血淋巴细胞和 43 例散发性结直肠癌的正常结肠组织中提取的基因组 DNA 进行 APC 基因第 15 外显子的突变检测。随后的测序用于确认突变位点。22 例 FAP 患者中有 5 例发现种系突变。所有这五个突变均显示碱基对缺失并导致产生截短蛋白。43 例散发性结直肠癌的正常组织中未发现截短的种系突变。蛋白质截短试验是一种灵敏且准确的技术,可检测截短突变,尤其是在 APC 基因的大外显子中。它可作为辅助 FAP 患者早期诊断的常规方法。