期刊
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
卷 350, 期 1, 页码 208-213出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2006.09.030
关键词
histone acetyltransferase; gene regulation; coactivators
The MYST acetyltransferase HBO1 is implicated in the regulation of DNA replication and activities of transcription factors such as the androgen receptor. Since the androgen receptor and NF-kappa B transcription factors crossmodulate their transcriptional activity, we investigated whether HBO1 regulates NF-kappa B signaling. Here, we report that in 293T cells HBO1 reduced dose-dependently NF-kappa B activity stimulated by TNF alpha, or by overexpressing p65/RelA, RelB, or cRel. Mutational analysis showed that the N-terminal serine-rich region of HBO1 but not the acetyltransferase function was required for inhibition. Electrophoretic mobility-shift assays demonstrated that HBO1 was neither perturbing the formation of p65/RelA DNA complexes nor binding itself to the kappa B consensus sequence or to p65/RelA, suggesting that HBO1 reduced NF-kappa B activity by squelching a cofactor. These data establish a novel function for HBO1 showing that it reduced NF-kappa B activity by sequestrating an essential coactivator from the NF-kappa B transcriptional complex. (c) 2006 Elsevier Inc. All rights reserved.
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