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Title: The role of kinetochore dynein in checkpoint silencing is restricted to disassembly of the corona
During mitosis, kinetochore–microtubule attachments are monitored by a molecular surveillance system known as the spindle assembly checkpoint. The prevailing model posits that dynein evicts checkpoint proteins (e.g., Mad1, Mad2) from stably attached kinetochores by transporting them away from kinetochores, thus contributing to checkpoint silencing. However, the mechanism by which dynein performs this function, and its precise role in checkpoint silencing remain unresolved. Here, we find that dynein’s role in checkpoint silencing is restricted to evicting checkpoint effectors from the fibrous corona, and not the outer kinetochore. Dynein evicts these molecules from the corona in a manner that does not require stable, end-on microtubule attachments. Thus, by disassembling the corona through indiscriminate microtubule encounters, dynein primes the checkpoint signaling apparatus so it can respond to stable end-on microtubule attachments and permit cells to progress through mitosis. Accordingly, we find that dynein function in checkpoint silencing becomes largely dispensable in cells in which checkpoint effectors are excluded from the corona.  more » « less
Award ID(s):
2107444
PAR ID:
10418157
Author(s) / Creator(s):
; ; ; ;
Editor(s):
Bloom, Kerry
Date Published:
Journal Name:
Molecular Biology of the Cell
Volume:
34
Issue:
7
ISSN:
1059-1524
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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