Chen Zhongzhou, Zang Jianye, Kappler John, Hong Xia, Crawford Frances, Wang Qin, Lan Fei, Jiang Chengyu, Whetstine Johnathan, Dai Shaodong, Hansen Kirk, Shi Yang, Zhang Gongyi
Department of Immunology, National Jewish Medical and Research Center, Denver, CO 80206, USA.
Proc Natl Acad Sci U S A. 2007 Jun 26;104(26):10818-23. doi: 10.1073/pnas.0704525104. Epub 2007 Jun 13.
The Jumonji C domain is a catalytic motif that mediates histone lysine demethylation. The Jumonji C-containing oxygenase JMJD2A specifically demethylates tri- and dimethylated lysine-9 and lysine-36 of histone 3 (H3K9/36 me3/2). Here we present structures of the JMJD2A catalytic core complexed with methylated H3K36 peptide substrates in the presence of Fe(II) and N-oxalylglycine. We found that the interaction between JMJD2A and peptides largely involves the main chains of the enzyme and the peptide. The peptide-binding specificity is primarily determined by the primary structure of the peptide, which explains the specificity of JMJD2A for methylated H3K9 and H3K36 instead of other methylated residues such as H3K27. The specificity for a particular methyl group, however, is affected by multiple factors, such as space and the electrostatic environment in the catalytic center of the enzyme. These results provide insights into the mechanisms and specificity of histone demethylation.
Jumonji C结构域是一种介导组蛋白赖氨酸去甲基化的催化基序。含Jumonji C的加氧酶JMJD2A特异性地使组蛋白3的赖氨酸-9和赖氨酸-36的三甲基化和二甲基化形式(H3K9/36 me3/2)去甲基化。在此,我们展示了在存在Fe(II)和N-草酰甘氨酸的情况下,JMJD2A催化核心与甲基化H3K36肽底物复合的结构。我们发现JMJD2A与肽之间的相互作用主要涉及酶和肽的主链。肽结合特异性主要由肽的一级结构决定,这解释了JMJD2A对甲基化H3K9和H3K36而非其他甲基化残基(如H3K27)的特异性。然而,对特定甲基基团的特异性受多种因素影响,如酶催化中心的空间和静电环境。这些结果为组蛋白去甲基化的机制和特异性提供了见解。