Medical Sciences, Indiana School of Medicine-Bloomington, Bloomington, IN 47405.
Department of Biology, Indiana University, Bloomington, IN 47405.
Mol Biol Cell. 2023 Apr 1;34(4):ar30. doi: 10.1091/mbc.E22-03-0113. Epub 2023 Feb 15.
Tight regulation of microtubule (MT) dynamics is necessary for proper spindle assembly and chromosome segregation. The MT destabilizing Kinesin-8, Kif18B, controls astral MT dynamics and spindle positioning. Kif18B interacts with importin α/β as well as with the plus-tip tracking protein EB1, but how these associations modulate Kif18B is not known. We mapped the key binding sites on Kif18B, made residue-specific mutations, and assessed their impact on Kif18B function. Blocking EB1 interaction disrupted Kif18B MT plus-end accumulation and inhibited its ability to control MT length on monopolar spindles in cells. Blocking importin α/β interaction disrupted Kif18B localization without affecting aster size. In vitro, importin α/β increased Kif18B MT association by increasing the on-rate and decreasing the off-rate from MTs, which stimulated MT destabilization. In contrast, EB1 promoted MT destabilization without increasing lattice binding in vitro, which suggests that EB1 and importin α/β have distinct roles in the regulation of Kif18B-mediated MT destabilization. We propose that importin α/β spatially modulate Kif18B association with MTs to facilitate its MT destabilization activity. Our results suggest that Ran regulation is important not only to control molecular motor function near chromatin but also to provide a spatial control mechanism to modulate MT binding of nuclear localization signal-containing spindle assembly factors.
微管(MT)动力学的严格调节对于正确的纺锤体组装和染色体分离是必要的。MT 不稳定的驱动蛋白-8(Kinesin-8)、Kif18B 控制着星体 MT 动力学和纺锤体定位。Kif18B 与导入蛋白 α/β 以及微管正端追踪蛋白 EB1 相互作用,但这些相互作用如何调节 Kif18B 尚不清楚。我们对 Kif18B 上的关键结合位点进行了作图,进行了残基特异性突变,并评估了它们对 Kif18B 功能的影响。阻断 EB1 相互作用会破坏 Kif18B MT 正端积累,并抑制其在细胞中单极纺锤体上控制 MT 长度的能力。阻断导入蛋白 α/β 相互作用会破坏 Kif18B 的定位,而不会影响星体的大小。在体外,导入蛋白 α/β 通过增加与 MT 的结合速率和降低解离速率来增加 Kif18B 与 MT 的结合,从而刺激 MT 去稳定化。相比之下,EB1 在体外促进 MT 去稳定化而不增加晶格结合,这表明 EB1 和导入蛋白 α/β 在调节 Kif18B 介导的 MT 去稳定化中具有不同的作用。我们提出,导入蛋白 α/β 空间调节 Kif18B 与 MT 的结合,以促进其 MT 去稳定化活性。我们的结果表明,Ran 调节不仅对控制靠近染色质的分子马达功能很重要,而且还提供了一种空间控制机制来调节核定位信号含有纺锤体组装因子与 MT 的结合。