Bachman Kurtis E, Park Ben Ho, Rhee Ina, Rajagopalan Harith, Herman James G, Baylin Stephen B, Kinzler Kenneth W, Vogelstein Bert
The Howard Hughes Medical Institute, The Sidney Kimmel Comprehensive Cancer Center, and Program in Cellular and Molecular Medicine, The Johns Hopkins University School of Medicine, 1650 Orleans Street, Baltimore, MD 21231, USA.
Cancer Cell. 2003 Jan;3(1):89-95. doi: 10.1016/s1535-6108(02)00234-9.
We attempted to answer two central questions about epigenetic silencing of the tumor suppressor gene p16(INK4a) in this study: (1) whether the maintenance of associated histone modifications is dependent on DNA methylation and (2) whether such histone modifications can occur prior to DNA methylation. By coupling chromatin immunoprecipitation with gene targeting and the analysis of specific alleles, we found that elimination of DNA methylation from a p16(INK4a) allele resulted in profound changes in surrounding histones. After continued passage of such cells, methylation of histone H3 lysine-9 occurred in conjunction with re-silencing in the absence of DNA methylation. These results have important implications for understanding the biochemical events underlying the silencing of tumor suppressor genes and the resultant growth suppression.
在本研究中,我们试图回答关于肿瘤抑制基因p16(INK4a)表观遗传沉默的两个核心问题:(1) 相关组蛋白修饰的维持是否依赖于DNA甲基化;(2) 此类组蛋白修饰是否能在DNA甲基化之前发生。通过将染色质免疫沉淀与基因靶向及特定等位基因分析相结合,我们发现从p16(INK4a)等位基因中去除DNA甲基化会导致周围组蛋白发生深刻变化。在这些细胞持续传代后,组蛋白H3赖氨酸-9的甲基化在无DNA甲基化的情况下伴随重新沉默而出现。这些结果对于理解肿瘤抑制基因沉默及由此产生的生长抑制背后的生化事件具有重要意义。