Ontology highlight
ABSTRACT:
SUBMITTER: Yang YW
PROVIDER: S-EPMC3921674 | biostudies-literature | 2014
REPOSITORIES: biostudies-literature
Yang Yul W YW Flynn Ryan A RA Chen Yong Y Qu Kun K Wan Bingbing B Wang Kevin C KC Lei Ming M Chang Howard Y HY
eLife 20140212
The WDR5 subunit of the MLL complex enforces active chromatin and can bind RNA; the relationship between these two activities is unclear. Here we identify a RNA binding pocket on WDR5, and discover a WDR5 mutant (F266A) that selectively abrogates RNA binding without affecting MLL complex assembly or catalytic activity. Complementation in ESCs shows that WDR5 F266A mutant is unable to accumulate on chromatin, and is defective in gene activation, maintenance of histone H3 lysine 4 trimethylation, ...[more]