Max Planck Institute of Biophysics, Frankfurt am Main, Germany.
Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Nature. 2023 Apr;616(7958):843-848. doi: 10.1038/s41586-023-05963-3. Epub 2023 Apr 19.
Structural maintenance of chromosomes (SMC) protein complexes are essential for the spatial organization of chromosomes. Whereas cohesin and condensin organize chromosomes by extrusion of DNA loops, the molecular functions of the third eukaryotic SMC complex, Smc5/6, remain largely unknown. Using single-molecule imaging, we show that Smc5/6 forms DNA loops by extrusion. Upon ATP hydrolysis, Smc5/6 reels DNA symmetrically into loops at a force-dependent rate of one kilobase pair per second. Smc5/6 extrudes loops in the form of dimers, whereas monomeric Smc5/6 unidirectionally translocates along DNA. We also find that the subunits Nse5 and Nse6 (Nse5/6) act as negative regulators of loop extrusion. Nse5/6 inhibits loop-extrusion initiation by hindering Smc5/6 dimerization but has no influence on ongoing loop extrusion. Our findings reveal functions of Smc5/6 at the molecular level and establish DNA loop extrusion as a conserved mechanism among eukaryotic SMC complexes.
染色体结构维持(SMC)蛋白复合物对于染色体的空间组织至关重要。尽管黏合蛋白和凝聚素通过挤出 DNA 环来组织染色体,但第三种真核 SMC 复合物 Smc5/6 的分子功能在很大程度上仍是未知的。我们使用单分子成像技术表明,Smc5/6 通过挤出形成 DNA 环。在 ATP 水解过程中,Smc5/6 以每秒一千碱基对的力依赖速度对称地将 DNA 卷入环中。Smc5/6 以二聚体的形式挤出环,而单体 Smc5/6 则沿 DNA 单向迁移。我们还发现,亚基 Nse5 和 Nse6(Nse5/6)作为环挤出的负调节剂。Nse5/6 通过阻碍 Smc5/6 二聚化来抑制环挤出的起始,但对正在进行的环挤出没有影响。我们的发现揭示了 Smc5/6 在分子水平上的功能,并确立了 DNA 环挤出是真核 SMC 复合物之间的保守机制。