Elimination by shedding

itotic spindle positioning involves a con-formational switch in LGN, the mammalian version of the invertebrate Pins protein, duces a spindle rocking that represents the first genetically manipulable model for studying spindle positioning in vertebrates. The switch operates via the opening of LGN, which can normally fold back onto itself. The unfolding is triggered by binding to either membrane-bound G ␣ i or NuMA, a protein that localizes to and stabilizes spindle poles. Unfolding was detected both as lack of self-binding and a mitotic reduction in FRET between fluorophores placed on either end of LGN. In the cell, binding of NuMA to LGN appears to be a prerequisite for further interactions, as in cells lacking NuMA the LGN never made it to the cortex. NuMA and its microtubule-bundling activity are nuclear during interphase. During mitosis, NuMA is liberated when the nuclear envelope is dissolved and can now pry apart cytoplasmic LGN. This makes the LGN–NuMA complex available for binding to G ␣ i on the membrane. Overexpressed G ␣ i or LGN induced rocking of the spindle, perhaps thanks to unequal pulling forces on the spindle. Macara hopes to sort out the basis for this rocking by visualizing the behaviors of individual microtubules near the cortex. Meanwhile, the rocking should be invaluable as a readout of spindle–cortex attachment. " It's artificial, " says Macara, " but it gives us a really powerful tool to look at forces on astral microtubules during mitosis. " WA) now report that localization can also be driven by degradation at every location but the target site. The protein in question is Cse4. This budding yeast homologue of CENP-A is localized specifically to kinetochores, where it incorporates into nucleosomes. It may be one of the initial (although not necessarily sufficient) building blocks of a kinetochore. Biggins noticed that Cse4 was marked for degradation by ubiquitin tags. A stable mutant of Cse4 was lethal and localized all over chromosome arms. By contrast, adding another degradation tag to Cse4 did not induce instability of the protein that had localized to the kinetochore. The Seattle group plans to delete various kinetochore proteins to see if any one of them is responsible for protecting kinetochore-localized Cse4 from degradation. They will also use the more abundant nondegradable Cse4 mutant to continue searching for a loading factor—a factor that probably complements the degradation system to achieve Cse4 localization. ynapse elimination occurs via a …