Anaphase-Promoting Complex/Cyclosome Participates in the Acute Response to Protein-Damaging Stress

Johanna K. Ahlskog, Johanna K. Björk, Alexandra N. Elsing, Camilla Aspelin, Marko Kallio, Pia Roos-Mattjus, Lea Sistonen

Research output: Contribution to journalArticleScientificpeer-review

18 Citations (Scopus)

Abstract

The ubiquitin E3 ligase anaphase-promoting complex/cyclosome (APC/C) drives degradation of cell cycle regulators in cycling cells by associating with the coactivators Cdc20 and Cdh1. Although a plethora of APC/C substrates have been identified, only a few transcriptional regulators are described as direct targets of APC/C-dependent ubiquitination. Here we show that APC/C, through substrate recognition by both Cdc20 and Cdh1, mediates ubiquitination and degradation of heat shock factor 2 (HSF2), a transcription factor that binds to the Hsp70 promoter. The interaction between HSF2 and the APC/C subunit Cdc27 and coactivator Cdc20 is enhanced by moderate heat stress, and the degradation of HSF2 is induced during the acute phase of the heat shock response, leading to clearance of HSF2 from the Hsp70 promoter. Remarkably, Cdc20 and the proteasome 20S core α2 subunit are recruited to the Hsp70 promoter in a heat shock-inducible manner. Moreover, the heat shock-induced expression of Hsp70 is increased when Cdc20 is silenced by a specific small interfering RNA (siRNA). Our results provide the first evidence for participation of APC/C in the acute response to protein-damaging stress.
Original languageEnglish
Pages (from-to)5608-5620
JournalMolecular and Cellular Biology
Volume30
Issue number24
DOIs
Publication statusPublished - 2010
MoE publication typeA1 Journal article-refereed

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Anaphase-Promoting Complex-Cyclosome
Heat-Shock Proteins
Hot Temperature
Shock
Ubiquitination
Heat-Shock Response
Ubiquitin-Protein Ligases
Proteasome Endopeptidase Complex
Small Interfering RNA
Cell Cycle
Transcription Factors

Cite this

Ahlskog, J. K., Björk, J. K., Elsing, A. N., Aspelin, C., Kallio, M., Roos-Mattjus, P., & Sistonen, L. (2010). Anaphase-Promoting Complex/Cyclosome Participates in the Acute Response to Protein-Damaging Stress. Molecular and Cellular Biology, 30(24), 5608-5620. https://doi.org/10.1128/MCB.01506-09
Ahlskog, Johanna K. ; Björk, Johanna K. ; Elsing, Alexandra N. ; Aspelin, Camilla ; Kallio, Marko ; Roos-Mattjus, Pia ; Sistonen, Lea. / Anaphase-Promoting Complex/Cyclosome Participates in the Acute Response to Protein-Damaging Stress. In: Molecular and Cellular Biology. 2010 ; Vol. 30, No. 24. pp. 5608-5620.
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abstract = "The ubiquitin E3 ligase anaphase-promoting complex/cyclosome (APC/C) drives degradation of cell cycle regulators in cycling cells by associating with the coactivators Cdc20 and Cdh1. Although a plethora of APC/C substrates have been identified, only a few transcriptional regulators are described as direct targets of APC/C-dependent ubiquitination. Here we show that APC/C, through substrate recognition by both Cdc20 and Cdh1, mediates ubiquitination and degradation of heat shock factor 2 (HSF2), a transcription factor that binds to the Hsp70 promoter. The interaction between HSF2 and the APC/C subunit Cdc27 and coactivator Cdc20 is enhanced by moderate heat stress, and the degradation of HSF2 is induced during the acute phase of the heat shock response, leading to clearance of HSF2 from the Hsp70 promoter. Remarkably, Cdc20 and the proteasome 20S core α2 subunit are recruited to the Hsp70 promoter in a heat shock-inducible manner. Moreover, the heat shock-induced expression of Hsp70 is increased when Cdc20 is silenced by a specific small interfering RNA (siRNA). Our results provide the first evidence for participation of APC/C in the acute response to protein-damaging stress.",
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Ahlskog, JK, Björk, JK, Elsing, AN, Aspelin, C, Kallio, M, Roos-Mattjus, P & Sistonen, L 2010, 'Anaphase-Promoting Complex/Cyclosome Participates in the Acute Response to Protein-Damaging Stress', Molecular and Cellular Biology, vol. 30, no. 24, pp. 5608-5620. https://doi.org/10.1128/MCB.01506-09

Anaphase-Promoting Complex/Cyclosome Participates in the Acute Response to Protein-Damaging Stress. / Ahlskog, Johanna K.; Björk, Johanna K.; Elsing, Alexandra N.; Aspelin, Camilla; Kallio, Marko; Roos-Mattjus, Pia; Sistonen, Lea.

In: Molecular and Cellular Biology, Vol. 30, No. 24, 2010, p. 5608-5620.

Research output: Contribution to journalArticleScientificpeer-review

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AB - The ubiquitin E3 ligase anaphase-promoting complex/cyclosome (APC/C) drives degradation of cell cycle regulators in cycling cells by associating with the coactivators Cdc20 and Cdh1. Although a plethora of APC/C substrates have been identified, only a few transcriptional regulators are described as direct targets of APC/C-dependent ubiquitination. Here we show that APC/C, through substrate recognition by both Cdc20 and Cdh1, mediates ubiquitination and degradation of heat shock factor 2 (HSF2), a transcription factor that binds to the Hsp70 promoter. The interaction between HSF2 and the APC/C subunit Cdc27 and coactivator Cdc20 is enhanced by moderate heat stress, and the degradation of HSF2 is induced during the acute phase of the heat shock response, leading to clearance of HSF2 from the Hsp70 promoter. Remarkably, Cdc20 and the proteasome 20S core α2 subunit are recruited to the Hsp70 promoter in a heat shock-inducible manner. Moreover, the heat shock-induced expression of Hsp70 is increased when Cdc20 is silenced by a specific small interfering RNA (siRNA). Our results provide the first evidence for participation of APC/C in the acute response to protein-damaging stress.

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