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

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

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 p150glued, 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.

Apa Reference Zhu, M., Settele, F., Kotak, S., Sanchez-Pulido, L., Ehret, L., Ponting, C.P., Gönczy, P. & Hoffmann, I. (2013). MISP is a novel Plk1 substrate required for proper spindle orientation and mitotic progression. Journal of Cell Biology, 200(6), 773-787. 10.1083/jcb.201207050
Doi 10.1083/jcb.201207050
Publication Date 18 Mar 2013
Publication Type Article
Researcher Luis Francisco Sánchez Pulido
Ontology Development
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