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DNA Replication: A Comprehensive Guide for Students, Study notes of Genetics

DNA replication is said to be semi-conservative because of this process of replication, where the resulting double helix is composed of both an old strand and ...

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2021/2022

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Genetics
DNA replication
DNA replication is the process in which a cell’s entire DNA is copied, or replicated. The identification of
the structure of DNA suggested that each strand of the double helix would serve as a template for
synthesis of a new strand. DNA replication process occurs during the Synthesis (S) phase of the eukaryotic
cell cycle. As each DNA strand has the same genetic information, both strands of the double helix can
serve as templates for the reproduction of a complementary new strand. The two resulting double
helices, which each contain one "old" strand and one "new" strand of DNA, are identical to the initial
double helix. DNA replication is said to be semi-conservative because of this process of replication, where
the resulting double helix is composed of both an old strand and a new strand.
The semi-conservative mechanism of replication was one of three models originally proposed for DNA
replication:
Semiconservative replication
would produce two copies that
each contained one of the original
strands and one new strand.
Conservative replication would
leave the two original template
DNA strands together in a double
helix, with the new DNA composed
entirely of two new strands.
Dispersive replication would
produce two copies of the DNA,
both containing a mixture of old
and new material.
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DNA replication

DNA replication is the process in which a cell’s entire DNA is copied, or replicated. The identification of the structure of DNA suggested that each strand of the double helix would serve as a template for synthesis of a new strand. DNA replication process occurs during the Synthesis (S) phase of the eukaryotic cell cycle. As each DNA strand has the same genetic information, both strands of the double helix can serve as templates for the reproduction of a complementary new strand. The two resulting double helices, which each contain one "old" strand and one "new" strand of DNA, are identical to the initial double helix. DNA replication is said to be semi-conservative because of this process of replication, where the resulting double helix is composed of both an old strand and a new strand.

The semi-conservative mechanism of replication was one of three models originally proposed for DNA replication: Semiconservative replication would produce two copies that each contained one of the original strands and one new strand. Conservative replication would leave the two original template DNA strands together in a double helix, with the new DNA composed entirely of two new strands. Dispersive replication would produce two copies of the DNA, both containing a mixture of old and new material.

DNA replication begins as an enzyme DNA helicase which breaks the hydrogen bonds holding the two strands together and forms a replication fork. The strands are held open by a single strand of binding proteins , preventing premature reannealing. Topoisomerase solves the problem caused by tension generated by winding/unwinding of DNA. This enzyme wraps around DNA and makes a cut permitting the helix to spin and relax. Once DNA is relaxed, topoisomerase reconnects broken strands. The resulting structure has two branching strands of DNA backbone with exposed bases. These exposed bases allow the DNA to be “read” by another enzyme, DNA polymerase , which then builds the complementary DNA strand. As DNA helicase continues to open the double helix, the replication fork grows.

The two new strands of DNA are “built” in opposite directions, through either a leading strand or a lagging strand. The leading strand is the DNA strand that DNA polymerase constructs in the 5' → 3' direction. This strand of DNA is made in a continuous manner, moving as the replication fork grows. The lagging strand is the DNA strand at the opposite side of the replication fork from the leading strand. It goes in the opposite direction, from 3' to 5'. DNA polymerase cannot build a strand in the 3' → 5' direction. Thus, this "lagging” strand is synthesized in short segments known as Okazaki fragments. On the lagging strand, an enzyme known as primase builds a short RNA primer. DNA polymerase is then able to use the free 3'-OH group on the RNA primer to make DNA in the 5' → 3' direction. The RNA fragments are then degraded and new DNA nucleotides are added to fill the gaps where the RNA was present. Another enzyme, DNA ligase , is then able to attach (ligate) the DNA nucleotides together, completing the synthesis of the lagging strand.

Many replication forks develop along a chromosome. This process continues until the replication forks meet, and the all of the DNA in a chromosome has been copied. Each new strand that has formed is complementary to the strand used as the template. Each resulting DNA molecule is identical to the original DNA molecule. During prophase of mitosis or prophase I of meiosis, these molecules of DNA condense into a chromosome made of two identical "sister" chromatids. This process ensures that cells that result from cell division have identical sets of genetic material , and that the DNA is an exact copy of the parent cell’s DNA.