Abstract
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.
Original language | English (US) |
---|---|
Pages (from-to) | 1735-1738 |
Number of pages | 4 |
Journal | Genes and Development |
Volume | 28 |
Issue number | 16 |
DOIs | |
State | Published - Aug 15 2014 |
Externally published | Yes |
Keywords
- Histone demethylase
- KDM2A
- Mechanism
- Substrate specificity
ASJC Scopus subject areas
- Genetics
- Developmental Biology