Molecular Insights into the Architecture of the Human SMC5/6 Complex

被引:25
|
作者
Adamus, M. [1 ,2 ]
Lelkes, E. [2 ]
Potesil, D. [1 ]
Ganji, S. R. [1 ]
Kolesar, P. [2 ]
Zabrady, K. [2 ]
Zdrahal, Z. [1 ,2 ]
Palecek, J. J. [1 ,2 ]
机构
[1] Masaryk Univ, Mendel Ctr Plant Genom & Prote, Cent European Inst Technol, Kamenice 5, Brno 62500, Czech Republic
[2] Masaryk Univ, Fac Sci, Natl Ctr Biomol Res, Kotlarska 2, Brno 61137, Czech Republic
关键词
human SMC5/6 complex architecture; SMC5-SMC6 dimer coiled-coil arms; NSE1-NSE3-NSE4; trimer; NSE5-NSE6; dimer; CANIN protein-protein interaction domain; MAGE domain; PROTEINS; COHESIN; CONDENSIN; SUBUNIT; KLEISIN; BINDING; FAMILY; ROLES;
D O I
10.1016/j.jmb.2020.04.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A family of Structural Maintenance of Chromosome (SMC) complexes is essential for key cellular processes ensuring proper cohesion, condensation and replication. They share a common SMC-kleisin architecture allowing them to embrace DNA. In SMC5/6, the NSE1 and NSE3 KITE and NSE4 kleisin subunits form a stable subcomplex that binds DNA and regulates essential processes. In addition, NSE5 and NSE6 subunits associate with the core SMC5/6 complex and recruit it to DNA repair sites. The architecture of the SMC5/6 complex is crucial for its proper functioning, and mutations within the human SMC5/6 subunits result in severe syndromes. Therefore, we aimed to analyze interactions within the human SMC5/6 complex and determine its detailed architecture. Firstly, we analyzed different parts of SMC5/6 by crosslinking and MS/MS analysis. Our data suggested domain arrangements of hNSE1-hNSE3 and orientation of hNSE4 within the hNSE1-hNSE3-hNSE4 subcomplex. The crosslinking and electron microscopic analysis of the SMC5/6 core complex showed its rod-like architecture with juxtaposed hSMC5-hSMC6 arms. Additionally, we observed fully or partially opened hSMC5-hSMC6 shapes with the hNSE1-hNSE3-hNSE4 trimer localized in the SMC head domains. To complete mapping of the human SMC5/6 complex architecture, we analyzed positions of hNSE5-hNSE6 at the hSMC5-hSMC6 arms. We showed that hNSE6 binding to hNSE5 and the coiled-coil arm of hSMC6 is mediated by a conserved FAM178 domain, which we therefore renamed CANIN (Coiled-coil SMC6 And NSE5 iNteracting) domain. Interestingly, hNSE6 bound both hSMC5 and hSMC6 arms, suggesting that hNSE6 may lock the arms and regulate the dynamics of the human SMC5/6 complex. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3820 / 3837
页数:18
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