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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