Here, we show that transcription factors bound to regulatory sequences can be identified by purifying these unique sequences directly from mammalian cells invivo. 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 γ-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 γ-globin gene expression. Reactivation of γ-globin gene expression ameliorates the symptoms of β-thalassemia and sickle cell disease, and these factors provide potential targets for the development of therapeutics for treating these patients

doi.org/10.1016/j.celrep.2013.07.004, hdl.handle.net/1765/57141
Cell Reports
Department of Cardio-Thoracic Surgery

Pourfarzad, F., Aghajanirefah, A., deBoer, E., TenHave, S., BrynvanDijk, T., Kheradmandkia, S., … Grosveld, F. (2013). Locus-specific proteomics by TChP: Targeted chromatin purification. Cell Reports, 4(3), 589–600. doi:10.1016/j.celrep.2013.07.004