Abstract

Kinetochore fibers (K-fibers) are microtubule bundles attached to chromosomes. Efficient K-fiber formation is required for chromosome congression, crucial for faithful chromosome segregation in cells. However, the mechanisms underlying K-fiber formation before chromosome biorientation remain unclear. Depletion of hepatoma up-regulated protein (HURP), a RanGTP-dependent microtubule-associated protein localized on K-fibers, has been shown to result in low-efficiency K-fiber formation. Therefore, here we sought to identify critical interaction partners of HURP that may modulate this function. Using co-immunoprecipitation and bimolecular fluorescence complementation assays, we determined that HURP interacts directly with the centrosomal protein transforming acidic coiled coil-containing protein 3 (TACC3), a centrosomal protein, both in vivo and in vitro through the HURP1-625 region. We found that HURP is important for TACC3 function during kinetochore microtubule assembly at the chromosome region in prometaphase. Moreover, HURP regulates stable lateral kinetochore attachment and chromosome congression in early mitosis by modulation of TACC3. These findings provide new insight into the coordinated regulation of K-fiber formation and chromosome congression in prometaphase by microtubule-associated proteins.

Highlights

  • Kinetochore fibers (K-fibers) are microtubule bundles attached to chromosomes

  • Our results demonstrated that FLAG-hepatoma up-regulated protein (HURP) and HA-transforming acidic coiled coil– containing protein 3 (TACC3) could interact with each other (Fig. 1C)

  • Our findings suggest that HURP and TACC3 co-regulate the status of KT–MT attachment, which is crucial for efficient chromosome congression and establishment of chromosome biorientation in mitotic cells

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Summary

ARTICLE cro

HURP regulates stable lateral kinetochore attachment and chromosome congression in early mitosis by modulation of TACC3 These findings provide new insight into the coordinated regulation of K-fiber formation and chromosome congression in prometaphase by microtubule-associated proteins. The transition function of the TACC3– ch-TOG– clathrin complex from MT polymerase activity to microtubule cross-linking activity is regulated by the activation of Aurora protein kinase A through TACC3 [34] It remains unclear how these kMT-localized proteins regulate K-fiber formation. Successful sorting and bundling as a result of this interaction promotes the formation of K-fibers, which is important for stable lateral attachment in prometaphase to ensure efficient chromosome congression and promote mitotic progression. Our study provides new insight into the coordinating mechanisms present between MAPs that promote successful K-fiber formation and chromosome congression in prometaphase

Results
Discussion
Cell culture and synchronization
Plasmid construction
Recombinant protein expression and pulldown experiment
Quantitative analyses of chromosome movement
Imaging processing and statistical analysis
Full Text
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