Projects per year
Abstract
Mitosis ensures equal segregation of the genome and is controlled by a variety of ubiquitylation signals on substrate proteins. However, it remains unexplored how the versatile ubiquitin code is read out during mitotic progression. Here, we identify the ubiquitin receptor protein UBASH3B as an important regulator of mitosis. UBASH3B interacts with ubiquitylated Aurora B, one of the main kinases regulating chromosome segregation, and controls its subcellular localization but not protein levels. UBASH3B is a limiting factor in this pathway and is sufficient to localize Aurora B to microtubules prior to anaphase. Importantly, targeting Aurora B to microtubules by UBASH3B is necessary for the timing and fidelity of chromosome segregation in human cells. Our findings uncover an important mechanism defining how ubiquitin attachment to a substrate protein is decoded during mitosis.
Original language | English |
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Pages (from-to) | 63-78 |
Number of pages | 16 |
Journal | Developmental Cell |
Volume | 36 |
Issue number | 1 |
DOIs | |
Publication status | Published - 11 Jan 2016 |
ASJC Scopus subject areas
- Developmental Biology
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Dive into the research topics of 'Ubiquitin Receptor Protein UBASH3B Drives Aurora B Recruitment to Mitotic Microtubules'. Together they form a unique fingerprint.Projects
- 1 Finished
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The Open Microscopy Environment: Image Informatics for Biological Sciences (Joint with Imperial College, Oxford University, Institut Pasteur, Carnegie-Mellon University, University of Wisconsin, Harvard Medical School & University of Edinburgh)
Swedlow, J. (Investigator)
1/10/11 → 30/09/16
Project: Research