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CpG/CpNpG motifs in the coding region are preferred sites for mutagenesis in the breast cancer susceptibility genes

机译:编码区的CpG / CpNpG基序是乳腺癌易感基因突变的首选位点

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摘要

The range of BRCA1/BRCA2 gene mutations is diverse and the mechanism accounting for this heterogeneity is obscure. To gain insight into the endogenous mutational mechanisms involved, we evaluated the association of specific sequences (i.e. CpG/CpNpG motifs, homonucleotides, short repeats) and mutations within the genes. We classified 1337 published mutations in BRCA1 (1765 BRCA2 mutations) for each specific sequence, and employed computer simulation combined with mathematical calculations to estimate the true underlying tendency of mutation occurrence. Interestingly, we found no mutational bias to homonucleotides and repeats in deletions/insertions and substitutions but striking bias to CpG/CpNpG in substitutions in both genes. This suggests that methylation-dependent DNA alterations would be a major mechanism for mutagenesis. © 2007 Federation of European Biochemical Societies.
机译:BRCA1 / BRCA2基因突变的范围是多种多样的,并且解释这种异质性的机制还不清楚。为了深入了解所涉及的内源性突变机制,我们评估了基因内特定序列(即CpG / CpNpG基序,同核苷酸,短重复序列)和突变之间的关联。我们为每个特定序列在BRCA1中分类了1337个已发布的突变(1765个BRCA2突变),并采用计算机模拟结合数学计算来估算突变发生的真正潜在趋势。有趣的是,我们在两个基因的缺失/插入和取代中均未发现对同核苷酸和重复序列的突变偏向,但在两个基因的取代中均对CpG / CpNpG产生了偏向。这表明甲基化依赖性DNA改变将是诱变的主要机制。 ©2007欧洲生物化学学会联合会。

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