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XB-ART-37218
Science 2008 Jan 25;3195862:469-72. doi: 10.1126/science.1148980.
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Centromeric Aurora-B activation requires TD-60, microtubules, and substrate priming phosphorylation.

Rosasco-Nitcher SE , Lan W , Khorasanizadeh S , Stukenberg PT .


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The chromosome passenger complex (CPC) controls chromosome congression, kinetochore-microtubule attachments, and spindle checkpoint signaling during mitosis. Aurora-B kinase is the catalytic subunit of the CPC. To understand how a single kinase can regulate such diverse events, we have investigated the activation of Aurora-B and describe two distinct activation mechanisms. First, Aurora-B activation in vitro requires two cofactors, telophase disc-60kD (TD-60) and microtubules. TD-60 is critical to localize both the CPC and Haspin kinase activity to centromeres and thus regulates Aurora-B at several levels. Second, Aurora-B substrates can inhibit kinase activation, and this is relieved by phosphorylation of these substrates by the centromeric kinases Plk1 and Haspin. These regulatory mechanisms suggest models for phosphorylation by Aurora-B of centromeric substrates at unaligned chromosomes and merotelic attachments.

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Species referenced: Xenopus
Genes referenced: haspin plk1 rcc2
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