4.7 Article

Characterization of HCP-6, a C-elegans protein required to prevent chromosome twisting and merotelic attachment

Journal

GENES & DEVELOPMENT
Volume 16, Issue 12, Pages 1498-1508

Publisher

COLD SPRING HARBOR LAB PRESS
DOI: 10.1101/gad.989102

Keywords

C. elegans; centromere; kinetochore; chromosome condensation; bipolar attachment; aneuploidy

Funding

  1. NCI NIH HHS [T32CA09657, T32 CA009657] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM048435, T32GM07270, T32 GM007270, R01GM48435-06] Funding Source: Medline

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Previous studies of mitosis show that capture of single kinetochores by microtubules from both centrosomes (merotelic orientation) is a major cause of aneuploidy. We have characterized hcp-6, a temperature-sensitive chromosome segregation mutant in C. elegans that exhibits chromosomes attached to both poles via a single sister kinetochore. We demonstrate that the primary defect in this mutant is a failure to fully condense chromosomes during prophase. Although centromere formation and sister centromere resolution remain unaffected in hcp-6, the chromosomes lack the rigidity of wild-type chromosomes and twist around the long axis of the chromosome. As such, they are unable to establish a proper orientation at prometaphase, allowing individual kinetochores to be captured by microtubules from both poles. We therefore propose that chromosome rigidity plays an essential role in maintaining chromosome orientation to prevent merotelic capture.

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