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J Cell Biol
2006 Jun 19;1736:829-31. doi: 10.1083/jcb.200605150.
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"HURP on" we're off to the kinetochore!
Wilde A
.
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RanGTP has a central role in spindle assembly, but the Ran-regulated factors required to initiate spindle bipolarity and stabilize MT growth toward the chromosomes remain unknown. However, three recent papers (Koffa et al., 2006; Sillje et al., 2006; Wong and Fang, 2006) have identified a single factor, HURP, that may encompass both of these properties.
Figure 1. HURP (red) is involved in stabilizing and targeting K-fibers to chromosomes (blue). Depletion of HURP leads to unstable K-fibers, which either fail to attach to kinetochores (black) or fail to generate tension between sister kinetochores; yet these cells eventually enter anaphase. Yellow depicts the gradient of RanGTP emanating from the chromosomes.
Figure 2. Model for the potential mode of action of the HURP complex. The components of the complex assemble in an MT-dependent or -independent manner. Once formed, Aurora A can phosphorylate components of the complex (arrows lead to known substrates of Aurora A). The complex may then function as a single entity or dissociate into smaller units to carry out specific functions in different parts of the spindle.
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