Department of Genetics, Development and Cell Biology, Iowa State University, Ames, Iowa, United States of America.
PLoS One. 2011 Apr 21;6(4):e18826. doi: 10.1371/journal.pone.0018826.
Large-scale sequencing of human cancer genomes and mouse transposon-induced tumors has identified a vast number of genes mutated in different cancers. One of the outstanding challenges in this field is to determine which genes, when mutated, contribute to cellular transformation and tumor progression. To identify new and conserved genes that drive tumorigenesis we have developed a novel cancer model in a distantly related vertebrate species, the zebrafish, Danio rerio. The Sleeping Beauty (SB) T2/Onc transposon system was adapted for somatic mutagenesis in zebrafish. The carp ß-actin promoter was cloned into T2/Onc to create T2/OncZ. Two transgenic zebrafish lines that contain large concatemers of T2/OncZ were isolated by injection of linear DNA into the zebrafish embryo. The T2/OncZ transposons were mobilized throughout the zebrafish genome from the transgene array by injecting SB11 transposase RNA at the 1-cell stage. Alternatively, the T2/OncZ zebrafish were crossed to a transgenic line that constitutively expresses SB11 transposase. T2/OncZ transposon integration sites were cloned by ligation-mediated PCR and sequenced on a Genome Analyzer II. Between 700-6800 unique integration events in individual fish were mapped to the zebrafish genome. The data show that introduction of transposase by transgene expression or RNA injection results in an even distribution of transposon re-integration events across the zebrafish genome. SB11 mRNA injection resulted in neoplasms in 10% of adult fish at ∼10 months of age. T2/OncZ-induced zebrafish tumors contain many mutated genes in common with human and mouse cancer genes. These analyses validate our mutagenesis approach and provide additional support for the involvement of these genes in human cancers. The zebrafish T2/OncZ cancer model will be useful for identifying novel and conserved genetic drivers of human cancers.
大规模的人类癌症基因组测序和小鼠转座子诱导的肿瘤已经鉴定出大量在不同癌症中发生突变的基因。该领域的一个突出挑战是确定哪些基因在发生突变时会导致细胞转化和肿瘤进展。为了鉴定新的和保守的驱动肿瘤发生的基因,我们在一种亲缘关系较远的脊椎动物斑马鱼(Danio rerio)中开发了一种新的癌症模型。睡眠美人(SB)T2/Onc 转座子系统被改编为斑马鱼的体细胞诱变。鲤鱼 β-肌动蛋白启动子被克隆到 T2/Onc 中,以创建 T2/OncZ。通过将线性 DNA 注射到斑马鱼胚胎中,分离出含有 T2/OncZ 大片段的两种转基因斑马鱼系。在 1 细胞期注射 SB11 转座酶 RNA,T2/OncZ 转座子从转基因阵列中在斑马鱼基因组中移动。或者,T2/OncZ 斑马鱼与稳定表达 SB11 转座酶的转基因系杂交。通过连接介导的 PCR 克隆 T2/OncZ 转座子整合位点,并在基因组分析仪 II 上进行测序。在单个鱼中,700-6800 个独特的整合事件被映射到斑马鱼基因组。数据表明,通过转基因表达或 RNA 注射引入转座酶会导致转座子重新整合事件在斑马鱼基因组中均匀分布。在大约 10 个月大时,SB11 mRNA 注射导致 10%的成年鱼发生肿瘤。T2/OncZ 诱导的斑马鱼肿瘤与人类和小鼠癌症基因具有许多共同的突变基因。这些分析验证了我们的诱变方法,并为这些基因参与人类癌症提供了额外的支持。斑马鱼 T2/OncZ 癌症模型将有助于鉴定人类癌症的新的和保守的遗传驱动因素。