Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/27466
Author(s): Lince-Faria, Mariana
Maffini, Stefano
Orr, Bernard
Ding, Yun
Florindo, Cláudia
Sunkel, CE
Tavares, Álvaro
Johansen, Jørgen
Johansen, Kristen M
Maiato, H
Title: Spatiotemporal control of mitosis by the conserved spindle matrix protein Megator
Issue Date: 2009
Abstract: A putative spindle matrix has been hypothesized to mediate chromosome motion, but its existence and functionality remain controversial. In this report, we show that Megator (Mtor), the Drosophila melanogaster counterpart of the human nuclear pore complex protein translocated promoter region (Tpr), and the spindle assembly checkpoint (SAC) protein Mad2 form a conserved complex that localizes to a nuclear derived spindle matrix in living cells. Fluorescence recovery after photobleaching experiments supports that Mtor is retained around spindle microtubules, where it shows distinct dynamic properties. Mtor/Tpr promotes the recruitment of Mad2 and Mps1 but not Mad1 to unattached kinetochores (KTs), mediating normal mitotic duration and SAC response. At anaphase, Mtor plays a role in spindle elongation, thereby affecting normal chromosome movement. We propose that Mtor/Tpr functions as a spatial regulator of the SAC, which ensures the efficient recruitment of Mad2 to unattached KTs at the onset of mitosis and proper spindle maturation, whereas enrichment of Mad2 in a spindle matrix helps confine the action of a diffusible “wait anaphase” signal to the vicinity of the spindle.
URI: http://hdl.handle.net/10216/27466
Catalogue Link: http://dx.doi.org/10.1083/jcb.200811012
Source: The Journal of Cell Biology, vol.184(5), p.647–657
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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