Jeppsson Kristian, Pradhan Biswajit, Sutani Takashi, Sakata Toyonori, Umeda Igarashi Miki, Berta Davide Giorgio, Kanno Takaharu, Nakato Ryuichiro, Shirahige Katsuhiko, Kim Eugene, Björkegren Camilla
Karolinska Institutet, Department of Cell and Molecular Biology, Biomedicum, Tomtebodavägen 16, 171 77 Stockholm, Sweden; Karolinska Institutet, Department of Biosciences and Nutrition, Neo, Hälsovägen 7c, 141 83 Huddinge, Sweden; Institute for Quantitative Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
Max Planck Institute of Biophysics, 60438 Frankfurt am Main, Germany.
Mol Cell. 2024 Mar 7;84(5):867-882.e5. doi: 10.1016/j.molcel.2024.01.005. Epub 2024 Jan 30.
The structural maintenance of chromosomes (SMC) protein complexes-cohesin, condensin, and the Smc5/6 complex (Smc5/6)-are essential for chromosome function. At the molecular level, these complexes fold DNA by loop extrusion. Accordingly, cohesin creates chromosome loops in interphase, and condensin compacts mitotic chromosomes. However, the role of Smc5/6's recently discovered DNA loop extrusion activity is unknown. Here, we uncover that Smc5/6 associates with transcription-induced positively supercoiled DNA at cohesin-dependent loop boundaries on budding yeast (Saccharomyces cerevisiae) chromosomes. Mechanistically, single-molecule imaging reveals that dimers of Smc5/6 specifically recognize the tip of positively supercoiled DNA plectonemes and efficiently initiate loop extrusion to gather the supercoiled DNA into a large plectonemic loop. Finally, Hi-C analysis shows that Smc5/6 links chromosomal regions containing transcription-induced positive supercoiling in cis. Altogether, our findings indicate that Smc5/6 controls the three-dimensional organization of chromosomes by recognizing and initiating loop extrusion on positively supercoiled DNA.
染色体结构维持(SMC)蛋白复合物——黏连蛋白、凝缩蛋白和Smc5/6复合物(Smc5/6)——对染色体功能至关重要。在分子水平上,这些复合物通过环挤压来折叠DNA。因此,黏连蛋白在间期形成染色体环,而凝缩蛋白使有丝分裂染色体浓缩。然而,Smc5/6最近发现的DNA环挤压活性的作用尚不清楚。在这里,我们发现Smc5/6在芽殖酵母(酿酒酵母)染色体上黏连蛋白依赖的环边界处与转录诱导的正超螺旋DNA相关联。从机制上讲,单分子成像显示Smc5/6二聚体特异性识别正超螺旋DNA螺旋的末端,并有效地启动环挤压,将超螺旋DNA聚集到一个大的螺旋环中。最后,Hi-C分析表明Smc5/6在顺式中连接包含转录诱导正超螺旋的染色体区域。总之,我们的研究结果表明,Smc5/6通过识别正超螺旋DNA并启动环挤压来控制染色体的三维组织。