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Cell Cycle 2017 Jun 18;16(12):1210-9

PP2A-B56gamma is required for an efficient spindle assembly checkpoint.

Varadkar P, Abbasi F, Takeda K, Dyson JJ, McCright B

Abstract

The Spindle Assembly Checkpoint (SAC) is part of a complex feedback system designed to ensure that cells do not proceed through mitosis unless all chromosomal kinetochores have attached to spindle microtubules. The formation of the kinetochore complex and the implementation of the SAC are regulated by multiple kinases and phosphatases. BubR1 is a phosphoprotein that is part of the Cdc20 containing mitotic checkpoint complex that inhibits the APC/C so that Cyclin B1 and Securin are not degraded, thus preventing cells going into anaphase. In this study, we found that PP2A in association with its B56¿ regulatory subunit, are needed for the stability of BubR1 during nocodazole induced cell cycle arrest. In primary cells that lack B56¿, BubR1 is prematurely degraded and the cells proceed through mitosis. The reduced SAC efficiency results in cells with abnormal chromosomal segregation, a hallmark of transformed cells. Previous studies on PP2A's role in the SAC and kinetochore formation were done using siRNAs to all five of the B56 family members. In our study we show that inactivation of only the PP2A-B56¿ subunit can affect the efficiency of the SAC. We also provide data that show the intracellular locations of the B56 subunits varies between family members, which is consistent with the hypothesis that they are not completely functionally redundant.


Category: Journal Article
PubMed ID: #28562161 DOI: 10.1080/15384101.2017.1325042
PubMed Central ID: #PMC5499913
Includes FDA Authors from Scientific Area(s): Biologics
Entry Created: 2017-01-31 Entry Last Modified: 2019-06-09
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