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  Paradoxical mitotic exit induced by a small molecule inhibitor of APC/C-Cdc20

Richeson, K. V., Bodrug, T., Sackton, K. L., Yamaguchi, M., Paulo, J. A., Gygi, S. P., et al. (2020). Paradoxical mitotic exit induced by a small molecule inhibitor of APC/C-Cdc20. Nature Chemical Biology, 16, 546-555. doi:10.1038/s41589-020-0495-z.

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 Creators:
Richeson, Katherine V.1, Author
Bodrug, Tatyana1, Author
Sackton, Katharine L.1, Author
Yamaguchi, Masaya1, Author
Paulo, Joao A.1, Author
Gygi, Steven P.1, Author
Schulman, Brenda A.2, Author           
Brown, Nicholas G.1, Author
King, Randall W.1, Author
Affiliations:
1external, ou_persistent22              
2Schulman, Brenda / Molecular Machines and Signaling, Max Planck Institute of Biochemistry, Max Planck Society, ou_2466699              

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Free keywords: ANAPHASE-PROMOTING COMPLEX/CYCLOSOME; SPINDLE-ASSEMBLY CHECKPOINT; CYCLIN B1; DESTRUCTION; ACTIVATION; CDC20; PROMETAPHASE; LOCALIZATION; DEGRADATION; PROGRESSION
 Abstract: The anaphase-promoting complex/cyclosome (APC/C) is a ubiquitin ligase that initiates anaphase and mitotic exit. APC/C is activated by Cdc20 and inhibited by the mitotic checkpoint complex (MCC), which delays mitotic exit when the spindle assembly checkpoint (SAC) is activated. We previously identified apcin as a small molecule ligand of Cdc20 that inhibits APC/C-Cdc20 and prolongs mitosis. Here we find that apcin paradoxically shortens mitosis when SAC activity is high. These opposing effects of apcin arise from targeting of a common binding site in Cdc20 required for both substrate ubiquitination and MCC-dependent APC/C inhibition. Furthermore, we found that apcin cooperates with p31(comet) to relieve MCC-dependent inhibition of APC/C. Apcin therefore causes either net APC/C inhibition, prolonging mitosis when SAC activity is low, or net APC/C activation, shortening mitosis when SAC activity is high, demonstrating that a small molecule can produce opposing biological effects depending on regulatory context.

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Language(s): eng - English
 Dates: 2020
 Publication Status: Published online
 Pages: 16
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: 000518737700003
DOI: 10.1038/s41589-020-0495-z
 Degree: -

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Title: Nature Chemical Biology
  Other : Nat. Chem. Biol.
Source Genre: Journal
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Publ. Info: New York, NY : Nature Pub. Group
Pages: - Volume / Issue: 16 Sequence Number: - Start / End Page: 546 - 555 Identifier: ISSN: 1552-4450
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000021290_1