Abstract
Histones form the protein core around which genomic DNA is wrapped in eukaryotic chromatin. Numerous genetic studies have established that the structure and transcriptional state of chromatin are closely related to histone post-translational modifications. Further elucidation of the precise mechanistic roles for individual histone modifications requires the ability to isolate and study homogeneously modified histones. However, the highly heterogeneous nature of histone modifications in vivo poses a significant challenge for such studies. Chemical tools that have enabled biochemical and biophysical studies of site-specifically modified histones are the focus of this minireview.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 11045-11050 |
| Number of pages | 6 |
| Journal | Journal of Biological Chemistry |
| Volume | 285 |
| Issue number | 15 |
| DOIs | |
| State | Published - Apr 9 2010 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Biochemistry
- Cell Biology