Rao Suhas S P, Huang Su-Chen, Glenn St Hilaire Brian, Engreitz Jesse M, Perez Elizabeth M, Kieffer-Kwon Kyong-Rim, Sanborn Adrian L, Johnstone Sarah E, Bascom Gavin D, Bochkov Ivan D, Huang Xingfan, Shamim Muhammad S, Shin Jaeweon, Turner Douglass, Ye Ziyi, Omer Arina D, Robinson James T, Schlick Tamar, Bernstein Bradley E, Casellas Rafael, Lander Eric S, Aiden Erez Lieberman
The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Cell. 2017 Oct 5;171(2):305-320.e24. doi: 10.1016/j.cell.2017.09.026.
The human genome folds to create thousands of intervals, called "contact domains," that exhibit enhanced contact frequency within themselves. "Loop domains" form because of tethering between two loci-almost always bound by CTCF and cohesin-lying on the same chromosome. "Compartment domains" form when genomic intervals with similar histone marks co-segregate. Here, we explore the effects of degrading cohesin. All loop domains are eliminated, but neither compartment domains nor histone marks are affected. Loss of loop domains does not lead to widespread ectopic gene activation but does affect a significant minority of active genes. In particular, cohesin loss causes superenhancers to co-localize, forming hundreds of links within and across chromosomes and affecting the regulation of nearby genes. We then restore cohesin and monitor the re-formation of each loop. Although re-formation rates vary greatly, many megabase-sized loops recovered in under an hour, consistent with a model where loop extrusion is rapid.
人类基因组折叠形成数千个区间,称为“接触结构域”,其内部呈现出增强的接触频率。“环状结构域”的形成是由于位于同一条染色体上的两个位点(几乎总是由CTCF和黏连蛋白结合)之间的拴系作用。当具有相似组蛋白标记的基因组区间共同分离时,“区室结构域”形成。在这里,我们研究了降解黏连蛋白的影响。所有环状结构域都被消除,但区室结构域和组蛋白标记均未受影响。环状结构域的丧失不会导致广泛的异位基因激活,但确实会影响相当少数的活跃基因。特别是,黏连蛋白的丧失会导致超级增强子共定位,在染色体内部和染色体之间形成数百个连接,并影响附近基因的调控。然后我们恢复黏连蛋白并监测每个环状结构的重新形成。尽管重新形成的速率差异很大,但许多兆碱基大小的环状结构在不到一小时内就恢复了,这与环状挤压迅速的模型一致。