Svaren J, Hörz W
Institut für Physiologische Chemie, Universität München, Germany.
Semin Cell Biol. 1995 Aug;6(4):177-83. doi: 10.1006/scel.1995.0025.
In this review, we summarize experiments which have used the yeast PHO5 gene to determine the functional consequences of nucleosome structure in the promoter region. In the PHO5 system, nucleosomes participate in promoter repression by interfering with factor binding. Therefore, disruption of nucleosome structure is likely a prerequisite for promoter activation. There still remain several important questions regarding the assembly and disassembly of chromatin repression. Recent experiments have shown that the PHO5 chromatin transition is replication and transcription independent. Nucleosome disruption does, however, depend upon binding of a transactivator, Pho4, to the PHO5 promoter. Moreover, the activation domain of Pho4 appears to play a critical role in chromatin disruption.
在本综述中,我们总结了利用酵母PHO5基因来确定启动子区域核小体结构功能后果的实验。在PHO5系统中,核小体通过干扰因子结合参与启动子抑制。因此,核小体结构的破坏可能是启动子激活的先决条件。关于染色质抑制的组装和拆卸仍存在几个重要问题。最近的实验表明,PHO5染色质转变与复制和转录无关。然而,核小体的破坏确实依赖于反式激活因子Pho4与PHO5启动子的结合。此外,Pho4的激活结构域似乎在染色质破坏中起关键作用。