Mapelli Marina, Massimiliano Lucia, Santaguida Stefano, Musacchio Andrea
Department of Experimental Oncology, European Institute of Oncology, Via Adamello 16, I-20139, Milan, Italy.
Cell. 2007 Nov 16;131(4):730-43. doi: 10.1016/j.cell.2007.08.049.
The 25 kDa Mad2 protein is a key player in the spindle assembly checkpoint, a safeguard against chromosome segregation errors in mitosis. Mad2 combines three unusual properties. First, Mad2 adopts two conformations with distinct topologies, open (O) and closed (C) Mad2. Second, C-Mad2 forms topological links with its two best-characterized protein ligands, Mad1 and Cdc20. Third, O-Mad2 and C-Mad2 engage in a "conformational" dimer that is essential for spindle checkpoint function in different organisms. The crystal structure of the O-Mad2-C-Mad2 conformational dimer, reported here, reveals an asymmetric interface that explains the selective dimerization of the O-Mad2 and C-Mad2 conformers. The structure also identifies several buried hydrophobic residues whose rearrangement correlates with the Mad2 topological change. The structure of the O-Mad2-C-Mad2 conformational dimer is consistent with a catalytic model in which a C-Mad2 template facilitates the binding of O-Mad2 to Cdc20, the target of Mad2 in the spindle checkpoint.
25 kDa的Mad2蛋白是纺锤体组装检验点中的关键因子,该检验点可防止有丝分裂过程中染色体分离错误。Mad2具有三个不同寻常的特性。其一,Mad2呈现出两种具有不同拓扑结构的构象,即开放型(O)Mad2和封闭型(C)Mad2。其二,C-Mad2与其两个最具特征的蛋白质配体Mad1和Cdc20形成拓扑连接。其三,O-Mad2和C-Mad2形成一种“构象”二聚体,这对于不同生物体中的纺锤体检验点功能至关重要。本文报道的O-Mad2-C-Mad2构象二聚体的晶体结构揭示了一个不对称界面,该界面解释了O-Mad2和C-Mad2构象异构体的选择性二聚化。该结构还确定了几个埋藏的疏水残基,其重排与Mad2拓扑变化相关。O-Mad2-C-Mad2构象二聚体的结构与一种催化模型一致,在该模型中,C-Mad2模板促进O-Mad2与Cdc20的结合(Cdc20是Mad2在纺锤体检验点中的作用靶点)。