ERRα protein is stabilized by LSD1 in a demethylation-independent manner

被引:23
作者
Carnesecchi, Julie [1 ,2 ]
Cerutti, Catherine [1 ]
Vanacker, Jean-Marc [1 ]
Forcet, Christelle [1 ]
机构
[1] Univ Lyon 1, Inst Genom Fonct Lyon, CNRS UMR5242, Ecole Normale Super Lyon, Lyon, France
[2] Heidelberg Univ, COS Heidelberg, Dept Dev Biol, Heidelberg, Germany
关键词
ESTROGEN-RELATED-RECEPTOR; CANCER-CELL-MIGRATION; BREAST-CANCER; PROSTATE-CANCER; GENE-EXPRESSION; IN-VIVO; TARGET; PROLIFERATION; METHYLATION; BIOMARKERS;
D O I
10.1371/journal.pone.0188871
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The LSD1 histone demethylase is highly expressed in breast tumors where it constitutes a factor of poor prognosis and promotes traits of cancer aggressiveness such as cell invasiveness. Recent work has shown that the Estrogen-Related Receptor a (ERR alpha) induces LSD1 to demethylate the Lys 9 of histone H3. This results in the transcriptional activation of a number of common target genes, several of which being involved in cellular invasion. High expression of ERR alpha protein is also a factor of poor prognosis in breast tumors. Here we show that, independently of its demethylase activities, LSD1 protects ERR alpha from ubiquitination, resulting in overexpression of the latter protein. Our data also suggests that the elevation of LSD1 mRNA and protein in breast cancer (as compared to normal tissue) may be a key event to increase ERRa protein, independently of its corresponding mRNA.
引用
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页数:12
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