Cell Biology
Chromatin Protein HP1α Interacts with the Mitotic Regulator Borealin Protein and Specifies the Centromere Localization of the Chromosomal Passenger Complex*

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Accurate mitosis requires the chromosomal passenger protein complex (CPC) containing Aurora B kinase, borealin, INCENP, and survivin, which orchestrates chromosome dynamics. However, the chromatin factors that specify the CPC to the centromere remain elusive. Here we show that borealin interacts directly with heterochromatin protein 1α (HP1α) and that this interaction is mediated by an evolutionarily conserved PXVXL motif in the C-terminal borealin with the chromo shadow domain of HP1α. This borealin-HP1α interaction recruits the CPC to the centromere and governs an activation of Aurora B kinase judged by phosphorylation of Ser-7 in CENP-A, a substrate of Aurora B. Consistently, modulation of the motif PXVXL leads to defects in CPC centromere targeting and aberrant Aurora B activity. On the other hand, the localization of the CPC in the midzone is independent of the borealin-HP1α interaction, demonstrating the spatial requirement of HP1α in CPC localization to the centromere. These findings reveal a previously unrecognized but direct link between HP1α and CPC localization in the centromere and illustrate the critical role of borealin-HP1α interaction in orchestrating an accurate cell division.

Cell Division
Chromosomes
Kinetochore
Mitosis
Protein Assembly

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*

This work was supported, in whole or in part, by National Institutes of Health Grants DK56292, CA164133, 8G12MD007602, and G12RR03034. This work was also supported by Chinese 973 Project Grants 2010CB912103, 2012CB917204, and 2013CB911203; by Chinese Academy of Sciences Grants KSCX1-YW-R-65 and KSCX2-YW-R-195; by Grant MOST 2009DFA31010; by Grants MOE 20113402130010 and IRT13038; by Chinese Natural Science Foundation Grants 91313303, 31320103904, 90508002, 91129714, 81270466, 31271518, 31371363, and 90913016; by China Fellowship 2012M510210; and by Fundamental Research Funds for Central Universities Grants WK2340000032 and WK2060190018.

1

Both authors contributed equally to this work.