let-7 miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching

The switch from fetal hemoglobin ( gamma- globin, HBG ) to adult hemoglobin ( beta- globin, HBB gene transcription in erythroid cells serves as a paradigm for a complex and clinically relevant developmental gene regulatory program. We previously identi fi ed HIC2 as regulator of the switch by inhibiting the transcription of BCL11A , a key repressor of HBG production. HIC2 is highly expressed in fetal cells, but the mechanism of its regulation unclear. Here we report that HIC2 developmental expression is controlled by microRNAs (miRNAs), as loss of global miRNA biogenesis through DICER1 depletion leads to upregulation of HIC2 and HBG messenger RNA. We identi fi ed the adult -expressed let miRNA family as a direct posttranscriptional regulator of HIC2 . Ectopic expression of let in fetal cells lowered HIC2 levels, whereas inhibition of let -7 in adult erythroblasts increased HIC2 production, culminating in decommissioning of a BCL11A erythroid enhancer and reduced BCL11A transcription. HIC2 depletion let -7 -inhibited cells restored BCL11A-mediated repression of HBG . Together, these data establish that fetal hemoglobin silencing in adult erythroid cells is under the control of a miRNA-mediated inhibitory pathway ( let -7 -I HIC2 BCL11A -I HBG ).