Montagna M, Santacatterina M, Corneo B, Menin C, Serova O, Lenoir G M, Chieco-Bianchi L, D'Andrea E
Institute of Oncology, University of Padua, Italy.
Cancer Res. 1996 Dec 1;56(23):5466-9.
We analyzed 16 Italian breast and breast/ovarian cancer families for BRCA1 germline mutations using a combination of the protein truncation test (PTT) and the single-strand conformation polymorphism techniques. Genomic DNA from the affected proband of each family was analyzed by applying the PTT to exon 11 of the BRCA1 gene. This initial screening led to the identification of truncated protein products in three families that were shown to carry three different frameshift mutations. In the families that scored negative in the PTT, single-strand conformation polymorphism analysis of the entire coding sequence of the gene revealed four additional mutations consisting of one nonsense, one in-frame deletion, one frameshift, and one missense mutation (in a family with a case of male breast cancer). The four frameshift mutations resulted in a decreased expression of the mutant allele, whereas no loss of transcript was associated with the other three mutations. All mutant alleles were shown to cosegregate with the cancer phenotype within the families, and none have previously been reported.
我们运用蛋白质截短试验(PTT)和单链构象多态性技术相结合的方法,对16个意大利乳腺癌及乳腺癌/卵巢癌家族进行了BRCA1基因种系突变分析。通过对每个家族中受影响的先证者的基因组DNA应用PTT检测BRCA1基因第11外显子,进行初步筛查。这一初步筛查在三个家族中鉴定出截短的蛋白质产物,显示这些家族携带三种不同的移码突变。在PTT检测呈阴性的家族中,对该基因整个编码序列进行单链构象多态性分析,又发现了另外四个突变,包括一个无义突变、一个框内缺失突变、一个移码突变和一个错义突变(在一个有男性乳腺癌病例的家族中)。这四个移码突变导致突变等位基因表达降低,而另外三个突变未伴有转录本缺失。所有突变等位基因在家族中均与癌症表型共分离,且此前均未被报道过。