Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Mol Cell. 2011 Oct 21;44(2):252-64. doi: 10.1016/j.molcel.2011.09.010.
We have determined the three-dimensional (3D) architecture of the Caulobacter crescentus genome by combining genome-wide chromatin interaction detection, live-cell imaging, and computational modeling. Using chromosome conformation capture carbon copy (5C), we derive ~13 kb resolution 3D models of the Caulobacter genome. The resulting models illustrate that the genome is ellipsoidal with periodically arranged arms. The parS sites, a pair of short contiguous sequence elements known to be involved in chromosome segregation, are positioned at one pole, where they anchor the chromosome to the cell and contribute to the formation of a compact chromatin conformation. Repositioning these elements resulted in rotations of the chromosome that changed the subcellular positions of most genes. Such rotations did not lead to large-scale changes in gene expression, indicating that genome folding does not strongly affect gene regulation. Collectively, our data suggest that genome folding is globally dictated by the parS sites and chromosome segregation.
我们通过结合全基因组染色质相互作用检测、活细胞成像和计算建模,确定了新月柄杆菌基因组的三维(3D)结构。使用染色体构象捕获碳拷贝(5C),我们得到了分辨率约为 13kb 的新月柄杆菌基因组的 3D 模型。这些模型表明,基因组呈椭圆形,带有周期性排列的臂。parS 位点是一对短的连续序列元件,已知它们参与染色体分离,位于一个极点,它们将染色体固定在细胞上,并有助于形成紧凑的染色质构象。重新定位这些元件导致染色体的旋转,从而改变了大多数基因的亚细胞位置。这样的旋转并没有导致大规模的基因表达变化,表明基因组折叠不会强烈影响基因调控。总的来说,我们的数据表明,基因组折叠是由 parS 位点和染色体分离决定的。