Boot Arnoud, Oosting Jan, Doorn Saskia, Ouahoud Sarah, Ventayol Garcia Marina, Ruano Dina, Morreau Hans, van Wezel Tom
Department of Pathology, Leiden University Medical Center, Leiden, Netherlands.
Int J Genomics. 2019 Apr 10;2019:1287671. doi: 10.1155/2019/1287671. eCollection 2019.
Allele-specific expression (ASE) is found in approximately 20-30% of human genes. During tumorigenesis, ASE changes due to somatic alterations that change the regulatory landscape. In colorectal cancer (CRC), many chromosomes show frequent gains or losses while homozygosity of chromosome 7 is rare. We hypothesized that genes essential to survival show allele-specific expression (ASE) on both alleles of chromosome 7. Using a panel of 21 recently established low-passage CRC cell lines, we performed ASE analysis by hybridizing DNA and cDNA to Infinium HumanExome-12 v1 BeadChips containing cSNPs in 392 chromosome 7 genes. The results of this initial analysis were extended and validated in a set of 89 paired normal mucosa and CRC samples. We found that 14% of genes showed ASE in one or more cell lines and identified of the potential cell survival genes , , and on chromosome 7, whereby the most abundantly expressed allele in the normal tissue is the lowest expressed allele in the tumor and vice versa. We established that this allelic switch does not result from loss of imprinting. The allelic switching of may be a result of transcriptional downregulation, while the exact mechanisms resulting in the allelic switching of and remain to be elucidated. In conclusion, our results show that profound changes take place in allelic transcriptional regulation during the tumorigenesis of CRC.
等位基因特异性表达(ASE)在约20%-30%的人类基因中存在。在肿瘤发生过程中,ASE会因改变调控格局的体细胞改变而发生变化。在结直肠癌(CRC)中,许多染色体显示出频繁的获得或缺失,而7号染色体的纯合性则很罕见。我们假设对生存至关重要的基因在7号染色体的两个等位基因上都表现出等位基因特异性表达(ASE)。我们使用一组21个最近建立的低传代CRC细胞系,通过将DNA和cDNA与包含392个7号染色体基因中cSNP的Infinium HumanExome-12 v1 BeadChips杂交来进行ASE分析。这一初步分析的结果在一组89对正常黏膜和CRC样本中得到了扩展和验证。我们发现14%的基因在一个或多个细胞系中表现出ASE,并在7号染色体上鉴定出了潜在的细胞存活基因、和,其中正常组织中表达最丰富的等位基因在肿瘤中是表达最低的等位基因,反之亦然。我们确定这种等位基因转换不是由印记丢失导致的。的等位基因转换可能是转录下调的结果,而导致和等位基因转换的确切机制仍有待阐明。总之,我们的结果表明,在CRC肿瘤发生过程中等位基因转录调控发生了深刻变化。