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首页> 外文期刊>Genome Biology >Systematic detection of putative tumor suppressor genes through the combined use of exome and transcriptome sequencing.
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Systematic detection of putative tumor suppressor genes through the combined use of exome and transcriptome sequencing.

机译:通过外显子组和转录组测序的组合使用系统检测推定的肿瘤抑制基因。

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摘要

To identify potential tumor suppressor genes, genome-wide data from exome and transcriptome sequencing were combined to search for genes with loss of heterozygosity and allele-specific expression. The analysis was conducted on the breast cancer cell line HCC1954, and a lymphoblast cell line from the same individual, HCC1954BL. RESULTS: By comparing exome sequences from the two cell lines, we identified loss of heterozygosity events at 403 genes in HCC1954 and at one gene in HCC1954BL. The combination of exome and transcriptome sequence data also revealed 86 and 50 genes with allele specific expression events in HCC1954 and HCC1954BL, which comprise 5.4% and 2.6% of genes surveyed, respectively. Many of these genes identified by loss of heterozygosity and allele-specific expression are known or putative tumor suppressor genes, such as BRCA1, MSH3 and SETX, which participate in DNA repair pathways. CONCLUSIONS: Our results demonstrate that the combined application of high throughput sequencing to exome and allele-specific transcriptome analysis can reveal genes with known tumor suppressor characteristics, and a shortlist of novel candidates for the study of tumor suppressor activities. Copyright 2010 Zhao et al.; licensee BioMed Central Ltd.
机译:为了鉴定潜在的肿瘤抑制基因,将来自外显子组和转录组测序的全基因组数据进行组合,以寻找具有杂合性缺失和等位基因特异性表达的基因。对乳腺癌细胞系HCC1954和来自同一个体的淋巴母细胞系HCC1954BL进行了分析。结果:通过比较两种细胞系的外显子组序列,我们确定了HCC1954中403个基因和HCC1954BL中一个基因的杂合性事件丢失。外显子组和转录组序列数据的结合还揭示了HCC1954和HCC1954BL中有等位基因特异性表达事件的86和50个基因,分别占所调查基因的5.4%和2.6%。通过杂合性丧失和等位基因特异性表达鉴定的许多这些基因是已知的或推定的抑癌基因,例如BRCA1,MSH3和SETX,它们参与DNA修复途径。结论:我们的结果表明,高通量测序在外显子组和等位基因特异性转录组分析中的结合应用可以揭示具有已知抑癌特征的基因,以及用于研究抑癌活性的新候选药物的候选清单。版权所有2010 Zhao等;被许可人BioMed Central Ltd.

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