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Originally published as MBC in Press, 10.1091/mbc.E07-03-0242 on July 5, 2007

Vol. 18, Issue 9, 3440-3450, September 2007

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A Novel Pathway that Coordinates Mitotic Exit with Spindle PositionFormula Formula

Scott A. Nelson, and John A. Cooper

Department of Cell Biology, Washington University in St. Louis, St. Louis, MO 63110

Submitted March 14, 2007; Accepted June 26, 2007
Monitoring Editor: Kerry Bloom

In budding yeast, the spindle position checkpoint (SPC) delays mitotic exit until the mitotic spindle moves into the neck between the mother and bud. This checkpoint works by inhibiting the mitotic exit network (MEN), a signaling cascade initiated and controlled by Tem1, a small GTPase. Tem1 is regulated by a putative guanine exchange factor, Lte1, but the function and regulation of Lte1 remains poorly understood. Here, we identify novel components of the checkpoint that operate upstream of Lte1. We present genetic evidence in agreement with existing biochemical evidence for the molecular mechanism of a pathway that links microtubule-cortex interactions with Lte1 and mitotic exit. Each component of this pathway is required for the spindle position checkpoint to delay mitotic exit until the spindle is positioned correctly.


This was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E07-03-0242) on July 5, 2007.

Formula Formula The online version of this article contains supplemental material at MBC Online (http://www.molbiolcell.org).

Address correspondence to: John Cooper (jcooper{at}wustl.edu).

Abbreviations used: SPC, spindle position checkpoint; MEN, mitotic exit network; GAP, GTPase-activating protein; GEF, guanine exchange factor; SPB, spindle pole body; FEAR, cdc14 early anaphase release; snRNP, small nuclear ribonucleoprotein; FLIP, fluorescence loss in photobleaching.




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