| Literature DB >> 27477906 |
Na Li1, Yuanyuan Li2, Jie Lv3, Xiangdong Zheng2, Hong Wen4, Hongjie Shen5, Guangjing Zhu6, Tsai-Yu Chen1, Shilpa S Dhar1, Pu-Yeh Kan1, Zhibin Wang6, Ramin Shiekhattar7, Xiaobing Shi4, Fei Lan5, Kaifu Chen3, Wei Li8, Haitao Li9, Min Gyu Lee10.
Abstract
Histone acetylation, including acetylated H3K14 (H3K14ac), is generally linked to gene activation. Monomethylated histone H3 lysine 4 (H3K4me1), together with other gene-activating marks, denotes active genes. In contrast to usual gene-activating functions of H3K14ac and H3K4me1, we here show that the dual histone modification mark H3K4me1-H3K14ac is recognized by ZMYND8 (also called RACK7) and can function to counteract gene expression. We identified ZMYND8 as a transcriptional corepressor of the H3K4 demethylase JARID1D. ZMYND8 antagonized the expression of metastasis-linked genes, and its knockdown increased the cellular invasiveness in vitro and in vivo. The plant homeodomain (PHD) and Bromodomain cassette in ZMYND8 mediated the combinatorial recognition of H3K4me1-H3K14ac and H3K4me0-H3K14ac by ZMYND8. These findings uncover an unexpected role for the signature H3K4me1-H3K14ac in attenuating gene expression and reveal a metastasis-suppressive epigenetic mechanism in which ZMYND8's PHD-Bromo cassette couples H3K4me1-H3K14ac with downregulation of metastasis-linked genes.Entities:
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Year: 2016 PMID： 27477906 PMCID： PMC4975651 DOI： 10.1016/j.molcel.2016.06.035
Source DB: PubMed Journal: Mol Cell ISSN： 1097-2765 Impact factor: 17.970