CENP-32 is required to maintain centrosomal dominance in bipolar spindle assembly

Shinya Ohta*, Laura Wood, Iyo Toramoto, Ken Ichi Yagyu, Tatsuo Fukagawa, William C. Earnshaw

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Centrosomes nucleate spindle formation, direct spindle pole positioning, and are important for proper chromosome segregation during mitosis in most animal cells. We previously reported that centromere protein 32 (CENP-32) is required for centrosome association with spindle poles during metaphase. In this study, we show that CENP-32 depletion seems to release centrosomes from bipolar spindles whose assembly they had previously initiated. Remarkably, the resulting anastral spindles function normally, aligning the chromosomes to a metaphase plate and entering anaphase without detectable interference from the free centrosomes, which appear to behave as free asters in these cells. The free asters, which contain reduced but significant levels of CDK5RAP2, show weak interactions with spindle microtubules but do not seem to make productive attachments to kinetochores. Thus CENP-32 appears to be required for centrosomes to integrate into a fully functional spindle that not only nucleates astral microtubules, but also is able to nucleate and bind to kinetochore and central spindle microtubules. Additional data suggest that NuMA tethers microtubules at the anastral spindle poles and that augmin is required for centrosome detachment after CENP-32 depletion, possibly due to an imbalance of forces within the spindle.

Original languageEnglish
Pages (from-to)1225-1237
Number of pages13
JournalMolecular Biology of the Cell
Volume26
Issue number7
Early online date5 Feb 2015
DOIs
Publication statusPublished - 15 Apr 2015

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