Université de Sciences et de Technologies de Lille, Interdisciplinary Research Institute, USR 3078 CNRS, Villeneuve d'Ascq, France.
Biophys J. 2011 Aug 17;101(4):L30-2. doi: 10.1016/j.bpj.2011.07.001.
For activation or repression of genes in eukaryotic organisms, the chromatin structure has to be adapted. This action is performed at least in part by dedicated motor proteins, the chromatin remodeling complexes. Recently, investigators have shown some interest in explaining how specific nucleosomes are targeted for chromatin remodeling. For this purpose, two kinetic proofreading scenarios for gene activation and repression have been put forward. We reanalyze both scenarios and show their common points and differences. Further, we propose that in gene repression by ISWI/ACF remodelers, which involves the generation of regular nucleosomal arrays, an additional proofreading step may be active.
为了在真核生物中激活或抑制基因,染色质结构必须进行适应。这种作用至少部分是由专门的马达蛋白,即染色质重塑复合物来完成的。最近,研究人员对解释如何针对特定核小体进行染色质重塑产生了一些兴趣。为此,提出了两种用于基因激活和抑制的动力学校对方案。我们重新分析了这两种情况,并展示了它们的共同点和不同点。此外,我们提出在由 ISWI/ACF 重塑酶介导的基因抑制中,可能存在一个额外的校对步骤,其中涉及到规则核小体阵列的生成。