Identification of an upstream enhancer containing an AML1 site in the human myeloperoxidase (MPO) gene

Abstract 

Myeloperoxidase (MPO) is an important antibacterial enzyme found only in granulocytes and monocytes. The human MPO gene is transcribed early during myelogenesis but MPO RNA synthesis ceases at the end of the promyelocyte stage of myeloid maturation. We recently identified a basal MPO promoter and several adjacent cis-elements in the proximal 5′-flanking region of this gene. Transfection studies using constructs containing several kb of 5′-flanking MPO DNA revealed the presence of a DNA segment located between bp (base pair) −4200 and bp −3800 with enhancer activity for the endogenous basal MPO promoter. Deletion studies revealed the core enhancer activity to lie between bp −4100 and bp −3844. The percentage enhancement of promoter activity is greater in MPO-expressing myeloid cells than in MPO-non-expressing myeloid cells or non-myeloid cells. Furthermore, the enhancer confers TPA- or DMSO-responsiveness upon either endogenous or exogenous promoters. DNase I footprinting and transfection experiments identified an AML1 site as a functionally important element within the enhancer. Gelshift competition and supershift experiments demonstrated the binding of the alpha subunit of the transcription factor AML1 to this site in HL-60 cells. This distal enhancer appears likely to play an important role in the control of MPO transcription during myeloid differentiation.

Abbreviations:  DTT, dithiothreitol, MPO, myeloperoxidase, PMSF, phenylmethylsulfonylfluoride, TPA, tetradecanoyl phorbol acetate, DMSO, dimethyl sulfoxide

Keywords:  Myeloperoxidase, cis-Elements, Enhancer, Promoter, Transcription, Gene regulation