Kanno Rieko, Janakiraman Harinarayanan, Kanno Masamoto
Department of Immunology, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3-Kasumi, Minami-ku, Hiroshima 734-8551, Japan.
Cancer Sci. 2008 Jun;99(6):1077-84. doi: 10.1111/j.1349-7006.2008.00797.x. Epub 2008 Apr 14.
The chromatin-associated Polycomb group (PcG) proteins were first identified in genetic screens for homeotic transformations in Drosophila melanogaster. Besides body patterning, members of the PcG are now known to regulate epigenetic cellular memory, stem cell self-renewal, and cancer development. Here, we discuss the multifarious functions of the PcG family, isoforms of protein complexes, and its enzymatic activities, for example histone methylation, links to DNA methylation, its phosphorylation status, H2A mono-ubiquitination, SUMOylation, and links to non-coding RNA. We also discuss the function of cytosolic PcG complexes as a regulator of receptor-induced actin polymerization and proliferation in a methylation-dependent manner. We propose that the functional versatility of PcG protein complexes contributed significantly to the complexity of heritable gene repression mechanisms, signal transduction, and cell proliferation in cancer development.
与染色质相关的多梳蛋白家族(PcG)最初是在黑腹果蝇同源异型转化的遗传筛选中被鉴定出来的。除了身体模式形成外,现在已知PcG成员还能调节表观遗传细胞记忆、干细胞自我更新和癌症发展。在这里,我们讨论了PcG家族的多种功能、蛋白质复合物的异构体及其酶活性,例如组蛋白甲基化、与DNA甲基化的联系、其磷酸化状态、H2A单泛素化、SUMO化以及与非编码RNA的联系。我们还讨论了胞质PcG复合物作为受体诱导的肌动蛋白聚合和增殖的甲基化依赖性调节剂的功能。我们认为,PcG蛋白复合物的功能多样性显著促成了癌症发展中可遗传基因抑制机制、信号转导和细胞增殖的复杂性。