Chakravarthy Srinivas, Park Young-Jun, Chodaparambil Jayanth, Edayathumangalam Rajeswari S, Luger Karolin
Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO 80523-1870, USA.
FEBS Lett. 2005 Feb 7;579(4):895-8. doi: 10.1016/j.febslet.2004.11.030.
It is now widely recognized that the packaging of genomic DNA, together with core histones, linker histones, and other functional proteins into chromatin profoundly influences nuclear processes such as transcription, replication, DNA repair, and recombination. Whereas earlier structural studies portrayed nucleosomes (the basic repeating unit of chromatin) as monolithic and static macromolecular assemblies, we now know that they are highly dynamic and capable of extensive crosstalk with the cellular machinery. Histone variants have evolved to locally alter chromatin structure, whereas histone chaperones and other cellular factors promote histone exchange and chromatin fluidity. Both of these phenomena likely facilitate interconversion between different chromatin states that show varying degrees of transcriptional activity.
现在人们普遍认识到,基因组DNA与核心组蛋白、连接组蛋白和其他功能蛋白包装成染色质,会深刻影响转录、复制、DNA修复和重组等核过程。早期的结构研究将核小体(染色质的基本重复单元)描绘为整体且静态的大分子组装体,而我们现在知道它们具有高度动态性,并且能够与细胞机制进行广泛的相互作用。组蛋白变体已经进化到可以局部改变染色质结构,而组蛋白伴侣和其他细胞因子则促进组蛋白交换和染色质流动性。这两种现象都可能促进不同染色质状态之间的相互转化,这些状态表现出不同程度的转录活性。