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XB-ART-9997
Mol Cell Biol 2000 Dec 01;2023:8643-54. doi: 10.1128/MCB.20.23.8643-8654.2000.
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Proteasome-mediated degradation of the coactivator p300 impairs cardiac transcription.

Poizat C , Sartorelli V , Chung G , Kloner RA , Kedes L .


Abstract
The transcription of tissue-specific genes is controlled by regulatory factors and cofactors and is suppressed in cardiac cells by the antineoplastic agent doxorubicin. Here we show that exposure of cultured cardiomyocytes to doxorubicin resulted in the rapid depletion of transcripts for MEF2C, dHAND, and NKX2.5, three pivotal regulators of cardiac gene expression. Delivery of exogenous p300, a coactivator of MEF2C and NKX2.5 in cardiomyocytes, restored cardiac transcription despite the presence of doxorubicin. Furthermore, p300 also restored the accumulation of transcripts for MEF2C itself. Importantly, cardiocytes exposed to doxorubicin displayed reduced levels of p300 proteins. This was not due to alterations in the level of p300 transcripts; rather, and surprisingly, doxorubicin promoted selective degradation of p300 mediated by the 26S-proteasome machinery. Doxorubicin had no effect on the general level of ubiquitinated proteins or on the levels of beta-catenin, a protein known to be degraded by proteasome-mediated degradation. These results provide evidence for a new mechanism of transcriptional repression caused by doxorubicin in which the selective degradation of p300 results in reduced p300-dependent transcription, including production of MEF2C mRNA.

PubMed ID: 11073966
PMC ID: PMC86467
Article link: Mol Cell Biol


Species referenced: Xenopus
Genes referenced: crebbp ep300 hand2 mef2c

References [+] :
Avantaggiati, The SV40 large T antigen and adenovirus E1a oncoproteins interact with distinct isoforms of the transcriptional co-activator, p300. 1996, Pubmed