DNA REPLICATION
• DNA replication is the process by which the genome's DNA is
copied in cells.
• Replication increases the DNA copies in the cells
• The entire genome is copied so that each new daughter cell
ends up with its own complete genome
PROCESS/STEPS IN DNA REPLICATION
1. Recognition of initiation point
- Starts at specific point called origin of replication (OR)
- Replication fork forms at OR
- OR is a nucleotide sequence of 100 to 200 pairs of bases.
- Specific initiation proteins recognize the initiation site on DNA
- Such proteins along with DNA directed RNA polymerase initiate the
synthesis of RNA primer
- RNA primer – responsible for the formation of DNA chain.
*IN prokaryotes – only one replication fork
*In Eukaryotes – several replication forks are formed
2. Unwinding of DNA –
• DNA duplex molecule is cut open (nicked) to form a bubble or fork
• unwinding proteins get attached at the point of nick
• Separation of the strands of the DNA duplex occurs
• Unwinding occurs in the presence of DNA HELICASE an enzyme.
3. Template DNA –
• The single stranded DNA on which the new DNA is synthesized is
called template DNA.
4. RNA Primer –
• RNA polymerase synthesizes RNA primer on template DNA
• In the absence of RNA primer the DNA replication is irregular.
5. Chain Elongation –
• New DNA strand is formed due to DNA polymerase III enzyme
• This enzyme adds nucleotides in 5’ to 3’ direction
• This activity of DNA polymerase is called polymerizing.
6. Replication forks –
• LEADING STRAND
- The strand of nascent DNA
- It is synthesized in the same direction as the growing replication fork.
- The synthesis of leading strand is continuous.
• LAGGING STRAND
- is the strand of new DNA whose direction is opposite to the direction of the growing
replication fork
- Replication of the lagging strand is more complicated
• It is synthesized in short, separated segments, which are then joined together by DNA ligase
to form a continuous DNA strand.
• OKAZAKI FRAGMENT
- Short pieces synthesized DNA on the lagging strand.
*Replication can be unidirectional or bi directional.
7. Proof reading –
• Errors made during the replication may lead to mutation
• The DNA polymerase I and polymerase III act as proof readers of the
newly formed DNA
• They move along the new synthesized DNA, read mistakes formed
due to improper base pairing
8. Removal of RNA primer and completion of DNA strand
• The RNA primer is removed by DNA polymerase I which synthesizes
a short segment of complimentary DNA to seal the gap
• Polymerase I remove the primer one nucleotide at a time and replace it
with complimentary deoxyribonucleotide.
9. Joining of fragments –
• Fragments are joined by DNA ligase
• A phosphodiesterase bond if formed between 3’ OH end of the
growing strand and 5’ end of the okazaki fragment.
DNA replication animations
https://www.youtube.com/watch?v=RLhwrFEtDEs
https://www.youtube.com/watch?v=3jslVQDGkLU
Protein Synthesis
https://www.youtube.com/watch?v=8wAwLwJAGHs
https://www.youtube.com/watch?v=bKIpDtJdK8Q