4.8 Article

Cryo-EM structure of DNA-bound Smc5/6 reveals DNA clamping enabled by multi-subunit conformational changes

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2202799119

Keywords

Smc5/6; DNA clamp; kleisin; KITE proteins; cryo-EM

Funding

  1. Leukemia Lymphoma Society
  2. Maloris Foundation
  3. NIH [R01GM131058, R35GM145260]
  4. A*STAR [212D800074]
  5. NIH Common Fund Transformative High Resolution Cryo-Electron Microscopy program [U24 GM129539]
  6. Simons Foundation [SF349247]
  7. NY State Assembly
  8. Beene Cancer Grant
  9. Memorial Sloan-Kettering Cancer Center Core Grant [P30-CA016086]

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In this study, the cryo-EM structure of DNA-bound Saccharomyces cerevisiae Smc5/6 complex was determined, revealing intricate interactions among core subunits and the mechanism of DNA binding. The Smc5/6 complex was found to form a clamp that encircles the DNA, with multiple subunits binding to DNA in a nonsequence-specific manner. These findings are significant for our understanding of the importance of SMC complexes in maintaining chromatin organization and function throughout the cell cycle.
Structural maintenance of chromosomes (SMC) complexes are essential for chromatin organization and functions throughout the cell cycle. The cohesin and condensin SMCs fold and tether DNA, while Smc5/6 directly promotes DNA replication and repair. The functions of SMCs rely on their abilities to engage DNA, but how Smc5/6 binds and translocates on DNA remains largely unknown. Here, we present a 3.8 angstrom cryogenic electron microscopy (cryo-EM) structure of DNA-bound Saccharomyces cerevisiae Smc5/6 complex containing five of its core subunits, including Smc5, Smc6, and the Nse1-3-4 subcomplex. Intricate interactions among these subunits support the formation of a clamp that encircles the DNA double helix. The positively charged inner surface of the clamp contacts DNA in a nonsequence-specific manner involving numerous DNA binding residues from four subunits. The DNA duplex is held up by Smc5 and 6 head regions and positioned between their coiled-coil arm regions, reflecting an engaged-head and open-arm configuration. The Nse3 subunit secures the DNA from above, while the hook-shaped Nse4 kleisin forms a scaffold connecting DNA and all other subunits. The Smc5/6 DNA clamp shares similarities with DNA-clamps formed by other SMCs but also exhibits differences that reflect its unique functions. Mapping cross-linking mass spectrometry data derived from DNA-free Smc5/6 to the DNA-bound Smc5/6 structure identifies multi-subunit conformational changes that enable DNA capture. Finally, mutational data from cells reveal distinct DNA binding contributions from each subunit to Smc5/6 chromatin association and cell fitness. In summary, our integrative study illuminates how a unique SMC complex engages DNA in supporting genome regulation.

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