Independence and interdependence of the three human aldolase A promoters in transgenic mice.

The human aldolase A gene is transcribed from three alternative promoters, clustered in a small 1.6-kb DNA domain. In transgenic mice, the upstream pN and the downstream pH promoters are ubiquitous, whereas the pM promoter, located between pN and pH, is activated specifically in fast skeletal muscles. A strong ubiquitous enhancer, lying upstream of the pH promoter, is necessary for both pN and pH ubiquitous activities, whereas a fast-muscle-specific enhancer, located upstream of the pM promoter, is required for pM-specific activation. In the present study, we use the transgenic mice model to further investigate the contribution of these two regulatory elements to the overall control of these three promoters. We confirm that the pM and pH promoters are activated independently of each other and, in particular, we show that the activation of pM in fast muscle is not responsible for the downregulation of the downstream pH in this tissue. By contrast, the pN promoter needs the presence of both enhancers to reproduce its correct pattern of activity and is unable to function autonomously in vivo.