Steps of DNA Replication
Steps of DNA Replication
Steps of DNA Replication
The first stage in replication is to separate the two DNA strands of the parental DNA molecule.
To unwind the DNA, positive superhelical turns have to be removed by cutting the DNA, and
allowing it to relax or by introducing negative superhelical turns to compensate for the positive
ones.
Replication fork:
During elongation, an enzyme called DNA polymerase adds DNA nucleotides to the 3′ end of the
newly synthesized polynucleotide strand.
DNA polymerases lack the ability to initiate a new strand and can only elongate a pre-existing
strand.
Unlike DNA polymerases, RNA polymerases can start new strands without any pre-existing 3’-
OH. A special RNA polymerase, known as primase, makes the RNA primers that are responsible
for strand initiation during DNA synthesis.
Leading strand :
The “leading strand” is synthesized continuously toward the replication fork as helicase unwinds the
template double-stranded DNA. The leading strand only needs to be started once.
Lagging strand:
The “lagging strand” is synthesized in the direction away from the replication fork and away from the
DNA helicase unwinds. the lagging strand is made in short sections and a new RNA primer must be
created each time a new portion is made. DNA polymerase then builds new strands of DNA starting
from each RNA primer
Okazaki fragments
Okazaki fragments are short sequences of DNA nucleotides which are synthesized
discontinuously and later linked together by the enzyme DNA ligase.
Termination of DNA replication occurs when two oppositely orientated replication forks
meet and fuse, to create two separate and complete double ‐stranded DNA molecules.
The replication termination protein (RTP) is one of only two well-defined proteins known
to be involved in arresting DNA replication forks.
the other being a protein known as tus (termination utilisation substance) from E. coli.