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Cryo-EM structures of Smc5/6 in multiple states reveal its assembly and functional mechanisms.
- Source :
-
Nature structural & molecular biology [Nat Struct Mol Biol] 2024 Oct; Vol. 31 (10), pp. 1532-1542. Date of Electronic Publication: 2024 Jun 18. - Publication Year :
- 2024
-
Abstract
- Smc5/6 is a member of the eukaryotic structural maintenance of chromosomes (SMC) family of complexes with important roles in genome maintenance and viral restriction. However, limited structural understanding of Smc5/6 hinders the elucidation of its diverse functions. Here, we report cryo-EM structures of the budding yeast Smc5/6 complex in eight-subunit, six-subunit and five-subunit states. Structural maps throughout the entire length of these complexes reveal modularity and key elements in complex assembly. We show that the non-SMC element (Nse)2 subunit supports the overall shape of the complex and uses a wedge motif to aid the stability and function of the complex. The Nse6 subunit features a flexible hook region for attachment to the Smc5 and Smc6 arm regions, contributing to the DNA repair roles of the complex. Our results also suggest a structural basis for the opposite effects of the Nse1-3-4 and Nse5-6 subcomplexes in regulating Smc5/6 ATPase activity. Collectively, our integrated structural and functional data provide a framework for understanding Smc5/6 assembly and function.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature America, Inc.)
- Subjects :
- Protein Conformation
Chromosomal Proteins, Non-Histone chemistry
Chromosomal Proteins, Non-Histone metabolism
Chromosomal Proteins, Non-Histone ultrastructure
Cryoelectron Microscopy
Saccharomyces cerevisiae Proteins chemistry
Saccharomyces cerevisiae Proteins metabolism
Saccharomyces cerevisiae Proteins ultrastructure
Cell Cycle Proteins metabolism
Cell Cycle Proteins chemistry
Cell Cycle Proteins ultrastructure
Saccharomyces cerevisiae metabolism
Models, Molecular
Subjects
Details
- Language :
- English
- ISSN :
- 1545-9985
- Volume :
- 31
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Nature structural & molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 38890552
- Full Text :
- https://doi.org/10.1038/s41594-024-01319-1