DNA Replication
DNA Replication
GENETICS
Prepared by:
Zuela C. Cabading
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RECAP
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DNA REPLICATION
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Learning Objectives
At the end of the lesson, the students should be able to:
a) explain the step-by-step process of DNA replication;
b) describe the roles of the enzymes involved in DNA
replication;
c) illustrate and label a diagram of DNA replication; and
d) share the importance of DNA replication by citing its role in
cellular function and inheritance, as well as its role in
preserving genetic information across generations.
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DNA REPLICATION
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DNA REPLICATION
The process by which a cell copies its DNA before it
divides. It ensures that each new cell gets an exact
copy of the DNA.
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Biological molecules, typically proteins, that act as
catalysts to speed up chemical reactions in the
body. Enzymes are highly specific – each catalyzes
a particular reaction or type of reaction.
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Initiation Stage
Elongation Stage
Termination Stage
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ELONGATION STAGE
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TERMINATION STAGE
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ELONGATION STAGE
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ELONGATION STAGE
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ELONGATION STAGE
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ELONGATION STAGE
ELONGATION STAGE
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TERMINATION STAGE
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STAGES PROCESSES
INITIATION
ELONGATION
TERMINATION
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STAGES PROCESSES
The process begins at specific sites called origins of replication. The enzyme helicase unwinds the DNA
double helix, creating a Y-shaped replication fork by separating the two strands. Single-strand binding
proteins then bind to the separated strands to keep them apart and prevent them from reannealing.
INITIATION As helicase continues to unwind the DNA, it causes supercoiling ahead of the replication fork.
Topoisomerase alleviates this tension by temporarily cutting the DNA strands, allowing them to
unwind, and then resealing the strands to maintain the DNA’s stability. Meanwhile, primase synthesizes
a short RNA primer to provide a starting point for DNA polymerase.
The synthesis of new DNA strands takes place. DNA polymerase III binds to the RNA primer and adds
complementary DNA nucleotides in the 5' to 3' direction, creating the new strands. Because the DNA
strands are antiparallel, replication occurs differently on each strand: the leading strand is synthesized
ELONGATION continuously in the same direction as the replication fork, while the lagging strand is synthesized
discontinuously in short segments known as Okazaki fragments. DNA polymerase III also possesses
proofreading capabilities, allowing it to check for and remove incorrectly paired nucleotides to
ensure accuracy. After the lagging strand is synthesized, DNA ligase joins the Okazaki fragments by
sealing the gaps, resulting in a continuous DNA strand.
The process concludes as the replication forks meet at specific termination sites, completing the
synthesis of new DNA strands. RNA primers used to initiate DNA synthesis are removed, typically by the
enzyme RNase H or DNA Polymerase I, and DNA polymerase III fills in the resulting gaps with DNA
TERMINATION nucleotides. Any remaining Okazaki fragments on the lagging strand are joined together by DNA
ligase to create a continuous DNA strand. Additionally, topoisomerase resolves any supercoiling or
intertwining of the DNA, ensuring that the two newly formed double helices can separate cleanly.
Finally, the proteins involved in replication, including DNA polymerases and helicase, are released,
allowing the new double-stranded DNA molecules to exist independently and ready for the next
phase of the cell cycle.
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Performance Task:
Create a DNA Replication model.
Submission Date: October 28, 2024
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Illustration of the 55LCC complex courtesy of Cameron
Baines (Phospho Biomedical Animation).
Biologists from the Perelman School of When 55LCC is absent, the researchers found
Medicine at the University of Pennsylvania and that replication is likely to become stuck, and
from the University of Leeds have identified a affected cells cease dividing.
multi-protein “machine” in cells that helps
govern the pausing or stopping of DNA
replication to ensure its smooth progress.