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  4. MISP is a novel Plk1 substrate required for proper spindle orientation and mitotic progression
 
research article

MISP is a novel Plk1 substrate required for proper spindle orientation and mitotic progression

Zhu, Mei
•
Settele, Florian
•
Kotak, Sachin  
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2013
The Journal of cell biology

Precise positioning of the mitotic spindle determines the correct cell division axis and is crucial for organism development. Spindle positioning is mediated through a cortical machinery by capturing astral microtubules, thereby generating pushing/pulling forces at the cell cortex. However, the molecular link between these two structures remains elusive. Here we describe a previously uncharacterized protein, MISP (C19orf21), as a substrate of Plk1 that is required for correct mitotic spindle positioning. MISP is an actin-associated protein throughout the cell cycle. MISP depletion led to an impaired metaphase-to-anaphase transition, which depended on phosphorylation by Plk1. Loss of MISP induced mitotic defects including spindle misorientation accompanied by shortened astral microtubules. Furthermore, we find that MISP formed a complex with and regulated the cortical distribution of the +TIP binding protein p150(glued), a subunit of the dynein-dynactin complex. We propose that Plk1 phosphorylates MISP, thus stabilizing cortical and astral microtubule attachments required for proper mitotic spindle positioning.

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Type
research article
DOI
10.1083/jcb.201207050
Author(s)
Zhu, Mei
Settele, Florian
Kotak, Sachin  
Sanchez-Pulido, Luis
Ehret, Lena
Ponting, Chris P.
Gönczy, Pierre  
Hoffmann, Ingrid
Date Issued

2013

Published in
The Journal of cell biology
Volume

200

Issue

6

Start page

773

End page

87

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
UPGON  
Available on Infoscience
June 27, 2013
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/93007
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