Promoters:

Two Promoter regions:

CAAT box - located 60-80 bases upstream of 5' end of the coding region

TATA (or Hogness) box - located 25 bases upstream

Gene transcription begins when RNA polymerase II attaches at one of these promoter sites in a process facilitated by numerous general transcription factors (In eukaryotes, RNA polymerase II alone is unable to recognize the TATA box).

Enhancers:

In contrast to promoters, enhancers increase the rate of transcription initiation

through protein binding and interactions with transcription factors bound to promoter

sequences.

Enhancers or repressors can be located  anywhere upstream, downstream or even within the transcribed gene.

Enzymes

Enzyme Function
DNA helicase Unwinds the DNA double helix at the replication fork
DNA topoisomerase Prevents supercoiling during replication Fluoroquinolones inhibit topoisomeras II (DNA gyrase) and topoisomerase IV
DNA polymerase III Only found in prokaryotes. Elongates the leading strand of DNA in a 5'-3' direction The 3'-5' exonuclease activity of DNA polymerase III proofreads the newly synthesised DNA strand
DNA polymerase I Only found in prokaryotes. Removes RNA primers (5' to 3' exonuclease activity) and replaces them with DNA
DNA ligase Seals up the fragments

Differences between DNA replication occurs in prokaryotes and eukaryotes

Prokaryotes Eukaryotes
Location of DNA replication Cytoplasm Nucleus
Origin of replication One Multiple

Multiple origins of replication make eukaryotic DNA synthesis quick and effective despite the large size of the genome compared to that of prokaryotic organisms.

Telomerase

a reverse transcriptase enzyme (RNA-dependent DNA polymerase) that adds TTAGGG repeats to the 3' end of DNA strands at the terminal end of chromosomes, the telomere region.