[Detection of germline mutations in the APC gene with the protein truncation test].

Xiao-Rong Liu, Xiang-Nian Shan, W Friedl, S Uhlhaas, Jin-Tian Li, P Propping, Ya-Ping Wang
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Abstract

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.

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【用蛋白截断法检测APC基因种系突变】。
为分析家族性腺瘤性息肉病(FAP)中起重要作用的大肠腺瘤性息肉病(APC)基因突变,建立了蛋白截断试验。检测APC突变位点与FAP患者临床特征之间的关系。采用PCR-TNT T7快速耦合转录/翻译系统,提取22例FAP患者外周血淋巴细胞和43例散发性结直肠癌正常结肠组织的基因组DNA,检测APC基因外显子15的突变。随后的测序用于确认突变位点。22例FAP患者中有5例发现生殖系突变。这5个突变均显示碱基对缺失,导致产生截断蛋白。43例散发性结直肠癌正常组织未发现截断性种系突变。蛋白截断试验是检测APC基因大外显子截断突变的一种灵敏、准确的技术。可作为辅助FAP患者早期诊断的常规方法。
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