Cairo Lucas V, Wozniak Richard W
Department of Cell Biology, University of Alberta, Edmonton, AB T6G 2H7, Canada.
Department of Cell Biology, University of Alberta, Edmonton, AB T6G 2H7, Canada.
Cell Rep. 2016 Mar 15;14(10):2440-50. doi: 10.1016/j.celrep.2016.02.041. Epub 2016 Mar 3.
The karyopherin (Kap) family of nuclear transport factors facilitates macromolecular transport through nuclear pore complexes (NPCs). The binding of Kaps to their cargos can also regulate, both temporally and spatially, the interactions of the cargo protein with interacting partners. Here, we show that the essential yeast Kap, Kap121, binds Dam1 and Duo1, components of the microtubule (MT)-associated Dam1 complex required for linking dynamic MT ends with kinetochores (KTs). Like mutations in the Dam1 complex, loss of Kap121 function compromises the formation of normal KT-MT attachments during mitosis. We show that the stability of the Dam1 complex in vivo is dependent on its association with Kap121. Furthermore, we show that the Kap121/Duo1 complex is maintained in the presence of RanGTP but Kap121 is released by the cooperative actions of RanGTP and tubulin. We propose that Kap121 stabilizes the Dam1 complex and participates in escorting it to spindle MTs.
核转运因子的核转运蛋白(Kap)家族促进大分子通过核孔复合体(NPC)进行转运。Kap与其货物的结合还可以在时间和空间上调节货物蛋白与其相互作用伙伴的相互作用。在这里,我们表明,酵母必需的Kap,即Kap121,与Dam1和Duo1结合,Dam1和Duo1是微管(MT)相关的Dam1复合体的组成部分,该复合体是将动态MT末端与动粒(KT)连接所必需的。与Dam1复合体中的突变一样,Kap121功能的丧失会损害有丝分裂期间正常KT-MT附着的形成。我们表明,Dam1复合体在体内的稳定性取决于其与Kap121的结合。此外,我们表明,Kap121/Duo1复合体在RanGTP存在的情况下得以维持,但Kap121会通过RanGTP和微管蛋白的协同作用而释放。我们提出,Kap121稳定Dam1复合体并参与将其护送至纺锤体MTs。