Barel D, Avigad S, Mor C, Fogel M, Cohen I J, Zaizov R
Cancer Molecular Genetics, Felsenstein Medical Research Center, Petah Tiqva, Israel.
Cancer Genet Cytogenet. 1998 May;103(1):1-6. doi: 10.1016/s0165-4608(97)00258-6.
We identified a novel germ-line p53 mutation in the noncoding, nonsplicing regions of a Li-Fraumeni family. Patients belonging to this family included pediatric medulloblastoma and rhabdomyosarcoma patients and a breast carcinoma patient. Three positions in the p53 gene were analyzed for loss of heterozygosity (LOH). One of the three loci retained heterozygosity, whereas the other two exhibited LOH. Sequence analysis of the third locus identified a change of 5'-CCGGGTGA-3' to 5'-CCAGGTTGGA-3', 63 bp downstream of exon 6. The mutation was identified in the germ line of the two pediatric patients and in each of the related parents. We excluded any additional mutation in the entire coding region of the p53 gene, including splice-site intronic sequences. Strong positive nuclear staining of the p53 protein was detected in both normal and tumor paraffin-embedded tissues. Eighty-five normal persons were negative for this alteration, which thus supports it as a mutation. These results may indicate that genetic changes within the noncoding region of the p53 gene may serve as an alternative mechanism of activating this gene. Mutations in the noncoding region of this gene should be further studied.
我们在一个李-佛美尼综合征家族的非编码、非剪接区域发现了一种新的种系p53突变。该家族的患者包括小儿髓母细胞瘤和横纹肌肉瘤患者以及一名乳腺癌患者。对p53基因的三个位点进行了杂合性缺失(LOH)分析。三个位点中的一个保持杂合性,而另外两个表现出杂合性缺失。对第三个位点的序列分析确定,在第6外显子下游63 bp处,序列从5'-CCGGGTGA-3'变为5'-CCAGGTTGGA-3'。在两名小儿患者及其相关父母的种系中均发现了该突变。我们排除了p53基因整个编码区域(包括剪接位点内含子序列)中的任何其他突变。在正常和肿瘤石蜡包埋组织中均检测到p53蛋白强烈的阳性核染色。85名正常人未出现这种改变,因此支持将其认定为一种突变。这些结果可能表明,p53基因非编码区域内的基因变化可能是激活该基因的另一种机制。该基因非编码区域的突变应进一步研究。