Molecular Cardiology Research Institute, Tufts Medical Center, Boston, MA 02111, USA.
Nucleic Acids Res. 2010 Jan;38(2):400-13. doi: 10.1093/nar/gkp1030. Epub 2009 Nov 11.
Nucleosome positioning plays a major role in controlling the accessibility of DNA to transcription factors and other nuclear processes. Nucleosome positions after assembly are at least partially determined by the relative affinity of DNA sequences for the histone octamer. Nucleosomes can be moved, however, by a class of ATP dependent chromatin remodeling complexes. We recently showed that the human SWI/SNF remodeling complex moves nucleosomes in a sequence specific manner, away from nucleosome positioning sequences (NPSes). Here, we compare the repositioning specificity of five remodelers of diverse biological functions (hSWI/SNF, the SNF2h ATPase and the hACF, CHRAC and WICH complexes than each contain SNF2h) on 5S rDNA, MMTV and 601 NPS polynucleosomal templates. We find that all five remodelers act similarly to reduce nucleosome occupancy over the strongest NPSes, an effect that could directly contribute to the function of WICH in activating 5S rDNA transcription. While some differences were observed between complexes, all five remodelers were found to result in surprisingly similar nucleosome distributions. This suggests that remodeling complexes may share a conserved repositioning specificity, and that their divergent biological functions may largely arise from other properties conferred by complex-specific subunits.
核小体定位在控制 DNA 对转录因子和其他核过程的可及性方面起着重要作用。组装后核小体的位置至少部分取决于 DNA 序列与组蛋白八聚体的相对亲和力。然而,核小体可以通过一类 ATP 依赖的染色质重塑复合物移动。我们最近表明,人 SWI/SNF 重塑复合物以序列特异性的方式移动核小体,远离核小体定位序列(NPSes)。在这里,我们比较了五种具有不同生物学功能的重塑酶(hSWI/SNF、SNF2h ATPase 和 hACF、CHRAC 和 WICH 复合物,它们都包含 SNF2h)在 5S rDNA、MMTV 和 601 NPS 多聚核小体模板上的重新定位特异性。我们发现,所有五种重塑酶都能类似地降低最强 NPSes 上的核小体占有率,这种效应可能直接有助于 WICH 激活 5S rDNA 转录的功能。虽然在复合物之间观察到一些差异,但发现所有五种重塑酶都导致了令人惊讶的相似的核小体分布。这表明重塑复合物可能具有保守的重新定位特异性,而它们不同的生物学功能可能主要来自于特定于复合物的亚基赋予的其他特性。