What is the explanation for transcription factors to bind to intronic regions downstream of the transcription start site?
Given that the most common model for transcriptional activation is that binding just upstream of the transcription start site (TSS) help place polymerase II at the beginning of the gene, what would be the reason to have binding sites for the same transcription factor peppered around introns in the same target genes?
My favourite gene had a bit of that: http://www.ncbi.nlm.nih.gov/pubmed/14623874 Maybe it makes sense for some TFs to be displaced by RNAPol