How substrate specificity is imposed on a histone demethylase-lessons from KDM2A

被引:10
|
作者
Tsai, Chi-Lin [1 ]
Shi, Yang [2 ,3 ]
Tainer, John A. [1 ,4 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Life Sci, Berkeley, CA 94720 USA
[2] Harvard Univ, Sch Med, Boston Childrens Hosp, Div Newborn Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[4] Scripps Res Inst, Skaggs Inst Chem Biol, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
histone demethylase; KDM2A; mechanism; substrate specificity; STRUCTURAL BASIS; TRIMETHYLLYSINE; RECOGNITION; JMJD2A; FAMILY;
D O I
10.1101/gad.249755.114
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Histone lysine methylation and demethylation regulate histone methylation dynamics, which impacts chromatin structure and function. To read and erase the methylated histone residues, lysine demethylases must specifically recognize the histone sequences and methylated sites and discriminate the degree of these methylations. In this issue of Genes & Development, Cheng and colleagues (pp. 1758-1771) determine a crystal structure of histone lysine demethylase KDM2A that specifically targets lower degrees of H3K36 methylation. The results reveal the structural basis for H3K36 substrate specificity and suggest mechanisms of Lys36 demethylation. This KDM2A-H3K36 complex structure, coupled with functional studies, provides needed insight into the process and regulation of histone demethylation.
引用
收藏
页码:1735 / 1738
页数:4
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