DNA replication
Stage one
The DNA is unwound and unzipped.
- the helix structure is unwound
- special molecules break the weak hydrogen bonds between bases, which are holding the two strands together
- this process occurs at several locations on a DNA molecule
Stage two
DNA polymerase adds the free DNA nucleotides to the 3’ end of the primer.
This uses complementary base pairing (A-T and C-G):
- adenine pairs with thymine
- thymine pairs with adenine
- cytosine pairs with guanine
- guanine pairs with cytosine
This allows the new DNA strand to form. A primer is needed to start replication.
- Leading strand is synthesised continuously:
- DNA polymerase adds nucleotides to the deoxyribose (3’) ended strand
- this happens in a 5’ to 3’ direction
- Lagging strand is synthesised in fragments:
- nucleotides cannot be added to the phosphate (5’) end because DNA polymerase can only add DNA nucleotides in a 5’ to 3’ direction
- the lagging strand is therefore synthesised in fragments
- the fragments are then sealed together by an enzyme called ligase
Stage three
The two new strands twist to form a double helix. Each is identical to the original strand.
Image caption, Replication starts with a single strand of DNA
Image caption, Stage one - The DNA strand is unwound and unzipped
Image caption, Stage two - Leading strand is synthesised continuously
Image caption, Stage two - Lagging strand is synthesised in fragments
Image caption, Stage two - Fragments are sealed together by ligase
Image caption, Stage three - Strands twist to form double helix
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