The microtubule-associated protein HURP recruits the centrosomal protein TACC3 to regulate K-fiber formation and support chromosome congression

J Biol Chem. 2018 Oct 5;293(40):15733-15747. doi: 10.1074/jbc.RA118.003676. Epub 2018 Jul 27.

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.

Keywords: HURP; TACC3; cell division; chromosome congression; chromosomes; kinetochore; kinetochore fiber; microtubule-associated protein (MAP); mitotic spindle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cell Cycle Proteins / antagonists & inhibitors
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Chromosome Positioning*
  • Chromosome Segregation
  • Gene Expression Regulation
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Kinetochores / metabolism
  • Kinetochores / ultrastructure
  • Microtubule-Associated Proteins / antagonists & inhibitors
  • Microtubule-Associated Proteins / genetics*
  • Microtubule-Associated Proteins / metabolism
  • Microtubules / metabolism*
  • Microtubules / ultrastructure
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Prometaphase*
  • Protein Transport
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Spindle Apparatus / metabolism
  • Spindle Apparatus / ultrastructure
  • Time-Lapse Imaging

Substances

  • Cell Cycle Proteins
  • DLGAP5 protein, human
  • Microtubule-Associated Proteins
  • NUF2 protein, human
  • Neoplasm Proteins
  • RNA, Small Interfering
  • TACC3 protein, human