Aberrant RNA splicing in the hMSH2 gene: molecular identification of three aberrant RNA in Scottish patients with colorectal cancer in the West of Scotland.

A Davoodi-Semiromi, G W Lanyon, R Davidson, M J Connor
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引用次数: 4

Abstract

Blood samples from 47 unselected patients with colorectal cancer were used as a source of hMSH2 mRNA. We identified three new hMSH2 aberrant mRNAs including: 1) IVS15 +5 G-->C resulting in exon 15 skipping from transcript; 2) an mRNA deletion of exons 2 to 6 inclusive; and 3) an mRNA deletion of exons 2 to 8 inclusive. In order to find out whether or not exon skipping is a natural consequence of alternative mRNA splicing, total RNA from 20 healthy individuals was converted to cDNA by reverse-transcriptase polymerase chain reaction, and our results show that none of the healthy individuals have the above aberrant mRNA. Our results also show that the presence of mutations in colorectal cancer cases, which do not fully meet the hereditary non-polyposis colon cancer criteria, would suggest that all familial cases should be investigated for germ line mutations in the mismatch repair genes.

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hMSH2基因中的异常RNA剪接:苏格兰西部结直肠癌患者中三种异常RNA的分子鉴定
来自47名未选择的结直肠癌患者的血液样本被用作hMSH2 mRNA的来源。我们发现了三种新的hMSH2异常mrna,包括:1)IVS15 + 5g ->C导致转录本外显子15跳过;2)外显子2至6的mRNA缺失;3)包括2至8外显子的mRNA缺失。为了确定外显子跳变是否是mRNA选择性剪接的自然结果,我们通过逆转录聚合酶链反应将20个健康个体的总RNA转化为cDNA,结果表明健康个体均没有上述异常mRNA。我们的研究结果还表明,在结直肠癌病例中存在不完全符合遗传性非息肉病性结肠癌标准的突变,这表明所有家族病例都应该调查错配修复基因的种系突变。
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