Center for Molecular Biology, University of Heidelberg, German Cancer Research Center-Center for Molecular Biology Alliance, Heidelberg, Germany.
J Cell Biol. 2021 Mar 1;220(3). doi: 10.1083/jcb.202004196.
The spindle pole body (SPB) provides microtubule-organizing functions in yeast and duplicates exactly once per cell cycle. The first step in SPB duplication is the half-bridge to bridge conversion via the antiparallel dimerization of the centrin (Cdc31)-binding protein Sfi1 in anaphase. The bridge, which is anchored to the old SPB on the proximal end, exposes free Sfi1 N-termini (N-Sfi1) at its distal end. These free N-Sfi1 promote in G1 the assembly of the daughter SPB (dSPB) in a yet unclear manner. This study shows that N-Sfi1 including the first three Cdc31 binding sites interacts with the SPB components Spc29 and Spc42, triggering the assembly of the dSPB. Cdc31 binding to N-Sfi1 promotes Spc29 recruitment and is essential for satellite formation. Furthermore, phosphorylation of N-Sfi1 has an inhibitory effect and delays dSPB biogenesis until G1. Taking these data together, we provide an understanding of the initial steps in SPB assembly and describe a new function of Cdc31 in the recruitment of dSPB components.
纺锤体极体 (SPB) 在酵母中提供微管组织功能,并且在每个细胞周期中准确复制一次。SPB 复制的第一步是通过后期中心体结合蛋白 Sfi1 的反平行二聚化将半桥转换为桥,该桥在近端锚定在旧的 SPB 上,在其远端暴露游离的 Sfi1 N 末端(N-Sfi1)。这些游离的 N-Sfi1 在 G1 中以一种尚未阐明的方式促进子 SPB (dSPB) 的组装。本研究表明,包括前三个 Cdc31 结合位点的 N-Sfi1 与 SPB 成分 Spc29 和 Spc42 相互作用,触发 dSPB 的组装。Cdc31 与 N-Sfi1 的结合促进了 Spc29 的招募,并且对于卫星的形成是必不可少的。此外,N-Sfi1 的磷酸化具有抑制作用,并延迟 dSPB 的生物发生直到 G1。综合这些数据,我们提供了对 SPB 组装初始步骤的理解,并描述了 Cdc31 在招募 dSPB 成分中的新功能。