A cytokinesis furrow is positioned by two consecutive signals

Henrik Bringmann () and Anthony A Hyman
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Henrik Bringmann: Max Planck Institute for Molecular Cell Biology and Genetics
Anthony A Hyman: Max Planck Institute for Molecular Cell Biology and Genetics

Nature, 2005, vol. 436, issue 7051, 731-734

Abstract: Abstract The position of the cytokinesis furrow in a cell determines the relative sizes of its two daughter cells as well as the distribution of their contents. In animal cells, the position of the cytokinesis furrow is specified by the position of the mitotic spindle1. The cytokinesis furrow bisects the spindle midway between the microtubule asters, at the site of the microtubule-based midzone, producing two daughter cells. Experiments in some cell types have suggested that the midzone positions the furrow2,3, but experiments in other cells have suggested that the asters position the furrow4,5. One possibility is that different organisms and cell types use different mechanisms to position the cytokinesis furrow. An alternative possibility is that both asters and the midzone contribute to furrow positioning6,7. Recent work in C. elegans has suggested that centrosome separation and the midzone are implicated in cytokinesis8. Here we examine the relative contributions of different parts of the mitotic spindle to positioning of the cytokinesis furrow in the C. elegans zygote. By spatially separating the spindle midzone from one of the asters using an ultraviolet laser, we show that the cytokinesis furrow is first positioned by a signal determined by microtubule asters, and then by a second signal that is derived from the spindle midzone. Thus, the position of the cytokinesis furrow is specified by two consecutive furrowing activities.

Date: 2005
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DOI: 10.1038/nature03823

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