Traceless semisynthesis of a set of histone 3 species bearing specific lysine methylation marks.

ABSTRACT: Considerable mechanistic insight into the function of histone post-translational modifications and the enzymes that install and remove them derives from in vitro experiments with modified histones, often embedded in nucleosomes. We report the first semisyntheses of native-like histone 3 (H3) bearing tri- and dimethyllysines at position 79 and trimethyllysine at position 36, as well as more facile and traceless semisyntheses of K9 and K27 trimethylated species. These semisyntheses are practical on a multi-milligram scale and can also generate H3 with combinations of marks. Each of these modifications has distinct functional consequences, although the pathways by which H3K36me3 and H3K79me2/3 act have not been entirely mapped. To this end, we demonstrated that our semisynthetic histones, whe

SUBMITTER: Chen Z 

PROVIDER: S-EPMC4415702 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature