4.6 Article

Feedback regulation of c-Myc by ribosomal protein L11

期刊

CELL CYCLE
卷 6, 期 22, 页码 2735-2741

出版社

TAYLOR & FRANCIS INC
DOI: 10.4161/cc.6.22.4895

关键词

ribosomal protein; L11; c-Myc; transcription; TRRAP; cell cycle

资金

  1. NCI NIH HHS [CA93614, K01 CA086957, R01 CA093614, K01-CA086957, CA 079721, R01-CA100855, R01 CA095441, K99 CA127134-01, R00 CA127134, CA095441, R01 CA100855, K990CA127134, R01 CA079721, K99 CA127134] Funding Source: Medline

向作者/读者索取更多资源

Several ribosomal proteins including L11 have been shown to activate p53 by inhibiting oncoprotein MDM2, leading to inhibition of cell cycle progression. Our recent study showed that L11 also inhibits oncoprotein c-Myc. Overexpression of L11 inhibits c-Myc-induced transcription and cell proliferation, while reduction of endogenous L11 increases these c-Myc activities. Interestingly, L11 is a transcriptional target of c-Myc, thus forming a negative feedback loop. We further showed that L11 competes with co-activator TRRAP for binding to c-Myc through the Myc box II (MB II) and reduces histone H4 acetylation at c-Myc target gene promoters. In addition, L11 appears to regulate c-Myc levels. Knocking down L11 markedly increases the mRNA and protein levels of endogenous c-Myc. These results suggest that L11 also inhibits cell cycle progression by regulating the c-Myc pathway. Here we further discuss the implications of this regulation and questions that this finding raises.

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