Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Trends Biochem Sci. 2018 Jun;43(6):469-478. doi: 10.1016/j.tibs.2018.03.006. Epub 2018 Apr 21.
Chromosomes are folded and compacted in interphase nuclei, but the molecular basis of this folding is poorly understood. Chromosome conformation capture methods, such as Hi-C, combine chemical crosslinking of chromatin with fragmentation, DNA ligation, and high-throughput DNA sequencing to detect neighboring loci genome-wide. Hi-C has revealed the segregation of chromatin into active and inactive compartments and the folding of DNA into self-associating domains and loops. Depletion of CTCF, cohesin, or cohesin-associated proteins was recently shown to affect the majority of domains and loops in a manner that is consistent with a model of DNA folding through extrusion of chromatin loops. Compartmentation was not dependent on CTCF or cohesin. Hi-C contact maps represent the superimposition of CTCF/cohesin-dependent and -independent folding states.
染色体在间期核中折叠和压缩,但这种折叠的分子基础还了解甚少。染色体构象捕获方法,如 Hi-C,将染色质的化学交联与片段化、DNA 连接和高通量 DNA 测序相结合,以检测全基因组的邻近基因座。Hi-C 揭示了染色质的分离成活跃和不活跃的隔室,以及 DNA 折叠成自我关联的域和环。最近的研究表明,CTCF、黏连蛋白或黏连蛋白相关蛋白的耗竭会以一种通过挤出染色质环来折叠 DNA 的模型一致的方式影响大多数结构域和环。隔室化并不依赖于 CTCF 或黏连蛋白。Hi-C 接触图谱代表了 CTCF/黏连蛋白依赖和独立折叠状态的叠加。