Loidl P
Institut für Medizinische Chemie und Biochemie, Universität Innsbruck, Austria.
FEBS Lett. 1988 Jan 25;227(2):91-5. doi: 10.1016/0014-5793(88)80874-3.
A model is presented which explains the biological function of posttranslational acetylation of core histones in chromatin. Along the lines of this model histone acetylation serves as a general mechanism to destabilize nucleosome core particles during various processes occurring in chromatin. Acetylation acts as a signal that modulates histone-protein and histone-DNA interactions and finally leads to the displacement of particular histones from nucleosome cores. The high specificity of the acetylation signal for different processes (DNA replication, transcription, differentiation-specific histone replacement) is achieved by site specificity and asymmetry of acetylation in nucleosomes. The essential features of this model are in accord with the more recent results on histone acetylation.
本文提出了一个模型,该模型解释了染色质中核心组蛋白翻译后乙酰化的生物学功能。按照这个模型,组蛋白乙酰化是一种在染色质发生的各种过程中使核小体核心颗粒不稳定的普遍机制。乙酰化作为一种信号,调节组蛋白-蛋白质和组蛋白-DNA相互作用,最终导致特定组蛋白从核小体核心中被置换出来。通过核小体中乙酰化的位点特异性和不对称性,实现了乙酰化信号对不同过程(DNA复制、转录、分化特异性组蛋白置换)的高度特异性。该模型的基本特征与最近关于组蛋白乙酰化的研究结果一致。