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Sensing Chromosome Bi-Orientation by Spatial Separation of Aurora B Kinase from Kinetochore Substrates
Dan Liu,1
Gerben Vader,2*
Martijn J. M. Vromans,2
Michael A. Lampson,1
Susanne M. A. Lens2
Abstract:
Successful cell division requires that chromosomes attach toopposite poles of the mitotic spindle (bi-orientation). AuroraB kinase regulates chromosome-spindle attachments by phosphorylatingkinetochore substrates that bind microtubules. Centromere tensionstabilizes bi-oriented attachments, but how physical forcesare translated into signaling at individual centromeres is unknown.Using fluorescence resonance energy transfer–based biosensorsto measure localized phosphorylation dynamics in living cells,we found that phosphorylation of an Aurora B substrate at thekinetochore depended on its distance from the kinase at theinner centromere. Furthermore, repositioning Aurora B closerto the kinetochore prevented stabilization of bi-oriented attachmentsand activated the spindle checkpoint. Thus, centromere tensioncan be sensed by increased spatial separation of Aurora B fromkinetochore substrates, which reduces phosphorylation and stabilizeskinetochore microtubules.
1 Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA. 2 Department of Medical Oncology, University Medical Center, 3584 CG Utrecht, Netherlands.
* Present address: Whitehead Institute for Biomedical Research,Cambridge, MA 02142, USA.
These authors contributed equally to this work.
To whom correspondence should be addressed. E-mail: lampson{at}sas.upenn.edu
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