Ausió Juan
Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC, Canada.
Brief Funct Genomic Proteomic. 2006 Sep;5(3):228-43. doi: 10.1093/bfgp/ell020. Epub 2006 May 10.
In recent years, the chromatin field has witnessed a renewed interest in histone variants as pertaining to their structural role, but mainly because of the functional specificity they impart to chromatin. In this review, I am going to discuss several of the most recent structural studies on core histone (H2A.Bbd, H2A.Z, H2A.X, macroH2A, H3.3, CENP-A) and linker histone variants (histone H1 microheterogeneity) focusing on their role in nucleosome stability and chromatin fibre dynamics with special emphasis on their possible functional implications. The data accumulated to date indicates that histone variability plays an important role in the histone-mediated regulation of chromatin metabolism. Understanding and deciphering the underlying structural amino acid code behind such variability remains one of the most exciting future challenges in chromatin research.
近年来,染色质领域对组蛋白变体重新产生了兴趣,这不仅涉及它们的结构作用,主要还因为它们赋予染色质的功能特异性。在这篇综述中,我将讨论一些关于核心组蛋白(H2A.Bbd、H2A.Z、H2A.X、macroH2A、H3.3、CENP - A)和连接组蛋白变体(组蛋白H1微异质性)的最新结构研究,重点关注它们在核小体稳定性和染色质纤维动力学中的作用,并特别强调其可能的功能影响。迄今为止积累的数据表明,组蛋白变异性在组蛋白介导的染色质代谢调控中起着重要作用。理解和破译这种变异性背后潜在的结构氨基酸密码仍然是染色质研究中最令人兴奋的未来挑战之一。