Fazzio Thomas G, Gelbart Marnie E, Tsukiyama Toshio
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Mail stop A1-162, P.O. Box 19024, 1100 Fairview Avenue North, Seattle, WA 98109-1024, USA.
Mol Cell Biol. 2005 Nov;25(21):9165-74. doi: 10.1128/MCB.25.21.9165-9174.2005.
We have previously shown that Saccharomyces cerevisiae Isw2 complex slides nucleosomes to remodel chromatin in vivo. Our data suggested a model in which Isw2 complex binds the histone octamer and DNA separately to generate the force necessary for nucleosome movement. Here we find that the histone H4 "basic patch" is the only portion of any amino-terminal histone tail required for both target-specific association of Isw2 complex with chromatin and chromatin remodeling in vivo, whereas it is dispensable for basal levels of chromatin binding. Similarly, we find that nonremodeled chromatin structure and integrity of Isw2 complex are required only for target-specific association of Isw2 with chromatin. These data demonstrate fundamental differences between the target-specific and basal modes of chromatin binding by Isw2 complex in vivo and suggest that only the former involves contributions from DNA, histone H4, and sequence-specific DNA binding proteins. We propose a model for target recognition and chromatin remodeling by Isw2 complex in vivo.
我们之前已经表明,酿酒酵母Isw2复合物在体内滑动核小体以重塑染色质。我们的数据提出了一个模型,即Isw2复合物分别结合组蛋白八聚体和DNA,以产生核小体移动所需的力。在这里,我们发现组蛋白H4“碱性补丁”是Isw2复合物与染色质在体内进行靶标特异性结合以及染色质重塑所必需的任何氨基末端组蛋白尾巴的唯一部分,而对于染色质结合的基础水平则是可有可无的。同样,我们发现未重塑的染色质结构和Isw2复合物的完整性仅对于Isw2与染色质的靶标特异性结合是必需的。这些数据证明了Isw2复合物在体内与染色质结合的靶标特异性模式和基础模式之间的根本差异,并表明只有前者涉及DNA、组蛋白H4和序列特异性DNA结合蛋白的作用。我们提出了一个Isw2复合物在体内进行靶标识别和染色质重塑的模型。