Abstract
Here, we show that transcription factors bound to regulatory sequences can be identified by purifying these unique sequences directly from mammalian cells in vivo. Using targeted chromatin purification (TChP), a double-pull-down strategy with a tetracycline-sensitive "hook" bound to a specific promoter, we identify transcription factors bound to the repressed gamma-globin gene-associated regulatory regions. After validation of the binding, we show that, in human primary erythroid cells, knockdown of a number of these transcription factors induces gamma-globin gene expression. Reactivation of gamma-globin gene expression ameliorates the symptoms of beta-thalassemia and sickle cell disease, and these factors provide potential targets for the development of therapeutics for treating these patients.
Original language | Undefined/Unknown |
---|---|
Pages (from-to) | 589-600 |
Number of pages | 12 |
Journal | Cell Reports |
Volume | 4 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2013 |
Research programs
- EMC MGC-02-13-02
- EMC MGC-02-21-01
- EMC ONWAR-01-94-01