Abstract
Successful cell division requires that chromosomes attach to opposite poles of the mitotic spindle (bi-orientation). Aurora B kinase regulates chromosome-spindle attachments by phosphorylating kinetochore substrates that bind microtubules. Centromere tension stabilizes bi-oriented attachments, but how physical forces are translated into signaling at individual centromeres is unknown. Using fluorescence resonance energy transfer-based biosensors to measure localized phosphorylation dynamics in living cells, we found that phosphorylation of an Aurora B substrate at the kinetochore depended on its distance from the kinase at the inner centromere. Furthermore, repositioning Aurora B closer to the kinetochore prevented stabilization of bi-oriented attachments and activated the spindle checkpoint. Thus, centromere tension can be sensed by increased spatial separation of Aurora B from kinetochore substrates, which reduces phosphorylation and stabilizes kinetochore microtubules.
| Original language | English |
|---|---|
| Pages (from-to) | 1350-3 |
| Number of pages | 4 |
| Journal | Science |
| Volume | 323 |
| Issue number | 5919 |
| DOIs | |
| Publication status | Published - 6 Mar 2009 |
| Externally published | Yes |
Keywords
- Aurora Kinase B
- Aurora Kinases
- Autoantigens/metabolism
- Biosensing Techniques
- Cell Line, Tumor
- Centromere/enzymology
- Centromere Protein A
- Chromatids/metabolism
- Chromosomal Proteins, Non-Histone/metabolism
- Chromosomes, Human/metabolism
- Fluorescence Resonance Energy Transfer
- HeLa Cells
- Humans
- Kinetochores/metabolism
- Microtubules/metabolism
- Mitosis
- Models, Biological
- Phosphorylation
- Protein Serine-Threonine Kinases/metabolism
- Recombinant Fusion Proteins/metabolism
- Spindle Apparatus/metabolism
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