Transcriptional enhancers are cis-acting DNA elements that are binding site
s for regulatory proteins and function at large distances from promoter ele
ments to stimulate transcription. Once thought to be. unique to eukaryotes,
enhancer-like elements have been discovered in a wide variety of bacteria.
The regulatory proteins that bind to these bacterial enhancers must contac
t RNA. polymerase to activate transcription, in principle, interactions bet
ween bacterial enhancer-binding proteins and RNA polymerase san occur by ei
ther DNA looping or tracking of the enhancer-binding protein along the DNA.
Paradigms for each of these methods are round in bacterial systems. Activa
tors of sigma (54)-RNA polymerase holoenzyme contact polymerase by DNA loop
ing, while bacteriophage T4 gp45 functions as a sliding clamp that tracks a
long DNA until it engages RNA polymerase. Significant advances have been ma
de over the last few veers towards understanding the mechanisms by which ba
cterial enhancer-binding proteins activate transcription, but important asp
ects of these mechanisms are still poorly defined.