Institute for Medical Engineering and Science, and Department of Physics, MIT, Cambridge, Massachusetts 02139, USA.
Howard Hughes Medical Institute, and Program in Systems Biology, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Cold Spring Harb Perspect Biol. 2022 Jul 1;14(7):a040147. doi: 10.1101/cshperspect.a040147.
Microscopy and genomic approaches provide detailed descriptions of the three-dimensional folding of chromosomes and nuclear organization. The fundamental question is how activity of molecules at the nanometer scale can lead to complex and orchestrated spatial organization at the scale of chromosomes and the whole nucleus. At least three key mechanisms can bridge across scales: (1) tethering of specific loci to nuclear landmarks leads to massive reorganization of the nucleus; (2) spatial compartmentalization of chromatin, which is driven by molecular affinities, results in spatial isolation of active and inactive chromatin; and (3) loop extrusion activity of SMC (structural maintenance of chromosome) complexes can explain many features of interphase chromatin folding and underlies key phenomena during mitosis. Interestingly, many features of chromosome organization ultimately result from collective action and the interplay between these mechanisms, and are further modulated by transcription and topological constraints. Finally, we highlight some outstanding questions that are critical for our understanding of nuclear organization and function. We believe many of these questions can be answered in the coming years.
显微镜和基因组方法提供了对染色体和核组织三维折叠的详细描述。基本问题是,分子在纳米尺度上的活性如何能够导致在染色体和整个核尺度上的复杂和协调的空间组织。至少有三个关键机制可以跨越尺度:(1)将特定基因座固定到核地标上会导致核的大规模重组;(2)由分子亲和力驱动的染色质的空间分隔导致活性和非活性染色质的空间隔离;(3)SMC(染色体结构维持)复合物的环挤出活性可以解释有丝分裂间期染色质折叠的许多特征,并构成有丝分裂过程中的关键现象。有趣的是,染色体组织的许多特征最终是由这些机制的集体作用和相互作用产生的,并受到转录和拓扑约束的进一步调节。最后,我们强调了一些对于我们理解核组织和功能至关重要的悬而未决的问题。我们相信,在未来几年内,这些问题中的许多都可以得到解答。