Martinez Danielle R, Richards Hunter W, Lin Qiushi, Torres-Cabala Carlos A, Prieto Victor G, Curry Jonathan L, Medrano Estela E
Huffington Center on Aging, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA ; Health Science Center, University of Texas, 6431 Fannin Street, Houston, TX 77030, USA.
J Skin Cancer. 2012;2012:823534. doi: 10.1155/2012/823534. Epub 2012 Nov 25.
The current study characterizes the mitosis-associated histone dual modification on the core of histone H3: trimethylation of histone H3 lysine 79 and simultaneous phosphorylation of H3 threonine 80 (H3K79me3T80ph). Through the use of protein and microscopy-based techniques, we find that H3K79me3T80ph shares a similar spatial and temporal regulation as H3S10ph but additionally requires methyltransferase activity. In addition, we find that Aurora kinase activity is necessary for the catalysis of H3K79me3T80ph in vivo. Finally, our analysis of H3K79me3T80ph using a tissue microarray indicates that H3K79me3T80ph marks a subset of primary cutaneous melanomas with metastatic potential indicating that H3K79me3T80ph may identify a subset of invasive melanomas with a more aggressive clinical behaviour.
当前研究对组蛋白H3核心区域与有丝分裂相关的组蛋白双重修饰进行了表征:组蛋白H3赖氨酸79三甲基化以及H3苏氨酸80同时磷酸化(H3K79me3T80ph)。通过使用基于蛋白质和显微镜的技术,我们发现H3K79me3T80ph与H3S10ph具有相似的时空调控,但另外还需要甲基转移酶活性。此外,我们发现极光激酶活性对于体内H3K79me3T80ph的催化是必需的。最后,我们使用组织微阵列对H3K79me3T80ph进行的分析表明,H3K79me3T80ph标记了具有转移潜能的原发性皮肤黑色素瘤的一个亚群,这表明H3K79me3T80ph可能识别出具有更侵袭性临床行为的侵袭性黑色素瘤亚群。