Efficient chromosome segregation during mitosis relies on the coordinated activity of
molecular motors with proteins that regulate kinetochore attachments to dynamic spindle
microtubules [1]. CLASPs are conserved kinetochore- and microtubule-associated
proteins encoded by two paralogue genes, clasp1 and clasp2, and have been previously
implicated in the regulation of kinetochore-microtubule dynamics [2-4]. However, it
remains unknown how CLASPs work in concert with other proteins to form a functional
kinetochore-microtubule interface. Here we have identified mitotic interactors of human
CLASP1 using a proteomic approach. Among these, the microtubule plus-end directed
motor CENP-E [5] was found to form a complex with CLASP1 that co-localizes to
multiple structures of the mitotic apparatus in human cells. We found that CENP-E
recruits both CLASP1 and CLASP2 to kinetochores independent of its motor activity or
the presence of microtubules. Depletion of CLASPs or CENP-E by RNAi in human cells
causes a significant and comparable reduction of kinetochore-microtubule poleward flux
and turnover rates, as well as rescues spindle bipolarity in Kif2a-depleted cells. We
conclude that CENP-E integrates two critical functions that are important for accurate
chromosome movement and spindle architecture: one relying directly on its motor
activity and the other involving the targeting of key microtubule regulators to
kinetochores
