Hesson Luke B, Sloane Mathew A, Wong Jason Wh, Nunez Andrea C, Srivastava Sameer, Ng Benedict, Hawkins Nicholas J, Bourke Michael J, Ward Robyn L
a Adult Cancer Program; Lowy Cancer Research Center and Prince of Wales Clinical School; UNSW ; Sydney , Australia.
Epigenetics. 2014 Oct;9(10):1422-30. doi: 10.4161/15592294.2014.970077.
Gene silencing in cancer frequently involves hypermethylation and dense nucleosome occupancy across promoter regions. How a promoter transitions to this silent state is unclear. Using colorectal adenomas, we investigated nucleosome positioning, DNA methylation, and gene expression in the early stages of gene silencing. Genome-wide gene expression correlated with highly positioned nucleosomes upstream and downstream of a nucleosome-depleted transcription start site (TSS). Hypermethylated promoters displayed increased nucleosome occupancy, specifically at the TSS. We investigated 2 genes, CDH1 and CDKN2B, which were silenced in adenomas but lacked promoter hypermethylation. Instead, silencing correlated with loss of nucleosomes from the -2 position upstream of the TSS relative to normal mucosa. In contrast, permanent CDH1 silencing in carcinoma cells was characterized by promoter hypermethylation and dense nucleosome occupancy. Our findings suggest that silenced genes transition through an intermediary stage involving altered promoter nucleosome positioning, before permanent silencing by hypermethylation and dense nucleosome occupancy.
癌症中的基因沉默通常涉及启动子区域的高甲基化和密集的核小体占据。启动子如何转变为这种沉默状态尚不清楚。我们利用结直肠腺瘤研究了基因沉默早期的核小体定位、DNA甲基化和基因表达。全基因组基因表达与核小体缺失的转录起始位点(TSS)上下游高度定位的核小体相关。高甲基化启动子显示核小体占据增加,特别是在TSS处。我们研究了两个基因,CDH1和CDKN2B,它们在腺瘤中沉默但缺乏启动子高甲基化。相反,沉默与相对于正常黏膜TSS上游-2位置的核小体丢失相关。相比之下,癌细胞中CDH1的永久沉默以启动子高甲基化和密集的核小体占据为特征。我们的研究结果表明,沉默基因在通过高甲基化和密集的核小体占据实现永久沉默之前,会经历一个涉及启动子核小体定位改变的中间阶段。