Published online 29 November 2004. doi:10.1083/jcb1675rr2
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 167, Number 5, 806-806
Rocking on Pins
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LGN opens to link NuMA and G i at the cortex.
MACARA/ELSEVIER
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Mitotic spindle positioning involves a conformational switch in LGN, the mammalian version of the invertebrate Pins protein, according to Quansheng Du and Ian Macara (University of Virginia, Charlottesville, VA). Interference with the switch induces 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 LGNNuMA 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 spindlecortex attachment. "It's artificial," says Macara, "but it gives us a really powerful tool to look at forces on astral microtubules during mitosis."
Reference:
Du, Q., et al. 2004. Cell. 119:503516.[CrossRef][Medline]
William A. Wells
wellsw{at}rockefeller.edu

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