Josep Carreras Leukaemia Research Institute, Campus Institut Català d'Oncologia - Germans Trias i Pujol, Campus Can Ruti, 08916 Badalona, Spain.
Program for Predictive and Personalized Medicine of Cancer, Germans Trias i Pujol Research Institute, 08916 Badalona, Spain.
Nat Rev Mol Cell Biol. 2017 May;18(5):299-314. doi: 10.1038/nrm.2016.166. Epub 2017 Feb 1.
Histone variants endow chromatin with unique properties and show a specific genomic distribution that is regulated by specific deposition and removal machineries. These variants - in particular, H2A.Z, macroH2A and H3.3 - have important roles in early embryonic development, and they regulate the lineage commitment of stem cells, as well as the converse process of somatic cell reprogramming to pluripotency. Recent progress has also shed light on how mutations, transcriptional deregulation and changes in the deposition machineries of histone variants affect the process of tumorigenesis. These alterations promote or even drive cancer development through mechanisms that involve changes in epigenetic plasticity, genomic stability and senescence, and by activating and sustaining cancer-promoting gene expression programmes.
组蛋白变体赋予染色质独特的性质,并表现出特定的基因组分布,这种分布受特定的沉积和去除机制调控。这些变体——特别是 H2A.Z、macroH2A 和 H3.3——在早期胚胎发育中具有重要作用,它们调控着干细胞的谱系分化,以及体细胞重编程为多能性的相反过程。最近的进展也揭示了组蛋白变体的突变、转录失调和沉积机制的变化如何影响肿瘤发生过程。这些改变通过改变表观遗传可塑性、基因组稳定性和衰老,以及激活和维持促进癌症的基因表达程序,促进甚至驱动癌症的发展。