Distinct distal and proximal p53-binding sites in the MCK promoter govern the transcriptional response to p53

Abstract

We have investigated the functional importance of nucleotide sequence differences between proximal (P-) and distal (D-) p53-binding elements in the MCK promoter. P- and D-elements normally co-operate to permit synergistic promoter activation by p53. Interestingly, we find that P-elements cannot co-operate with each other. In contrast, co-operation between D-binding sites results in levels of p53-induced transcription far higher than those obtained by co-operation between P- and D-elements. These studies imply that distinct D- and P-p53-binding sites in the MCK promoter may dictate the promoter response to p53.