Cells Can Replicate Their DNA Precisely

A schematic shows a double-stranded DNA molecule undergoing the replication process. At right, the
double helix has opened and the top strand has separated from the bottom. A globular yellow structure,
representing the protein helicase, is bound to the ends of several nitrogenous bases on the lower
strand.

Replication is the process by which a double-stranded DNA molecule is copied to produce two identical
DNA molecules. DNA replication is one of the most basic processes that occurs within a cell. Each time a
cell divides, the two resulting daughter cells must contain exactly the same genetic information, or DNA,
as the parent cell. To accomplish this, each strand of existing DNA acts as a template for replication.

How is DNA replicated?

Replication occurs in three major steps: the opening of the double helix and separation of the DNA
strands, the priming of the template strand, and the assembly of the new DNA segment. During
separation, the two strands of the DNA double helix uncoil at a specific location called the origin. Several
enzymes and proteins then work together to prepare, or prime, the strands for duplication. Finally, a
special enzyme called DNA polymerase organizes the assembly of the new DNA strands. The following
description of this three-stage process applies generally to all cells, but specific variations within the
process may occur depending on organism and cell type.

What triggers replication?

A schematic shows a double-stranded DNA molecule undergoing the replication process. The left side of
the molecule is double-stranded. In the middle of the molecule, a globular yellow structure,
representing the protein helicase, is bound to the ends of several nitrogenous bases on the lower
strand. To the right of the helicase protein, the double helix has opened and the top strand has
separated from the bottom. At right, a short segment of the newly replicated double-stranded DNA
molecule is visible.

Figure 1: Helicase (yellow) unwinds the double helix.

The initiation of DNA replication occurs in two steps. First, a so-called initiator protein unwinds a short
stretch of the DNA double helix. Then, a protein known as helicase attaches to and breaks apart the
hydrogen bonds between the bases on the DNA strands, thereby pulling apart the two strands. As the
helicase moves along the DNA molecule, it continues breaking these hydrogen bonds and separating the
two polynucleotide chains (Figure 1).

A schematic shows a double-stranded DNA molecule undergoing the replication process. At right, the
double helix has opened and the top strand has separated from the bottom. A globular yellow structure,
representing the protein helicase, is bound to the ends of several nitrogenous bases on the lower
strand. A red globular molecule, representing the enzyme primase, is bound to the lower DNA strand to
the right of helicase.
Figure 2: While helicase and the initiator protein (not shown) separate the two polynucleotide chains,
primase (red) assembles a primer. This primer permits the next step in the replication process.

Figure Detail

Meanwhile, as the helicase separates the strands, another enzyme called primase briefly attaches to
each strand and assembles a foundation at which replication can begin. This foundation is a short
stretch of nucleotides called a primer (Figure 2).

How are DNA strands replicated?

A schematic shows a region of horizontal single-stranded DNA. A transparent blue globular structure,
representing the enzyme DNA polymerase, is bound to a seven-nucleotide-long region on the right-hand
side of the DNA strand. The region of DNA bound by DNA polymerase is visible inside the transparent
enzyme at a higher magnification. Six nucleotides in this region are bound to six complementary
nucleotides arranged above and in parallel to the single strand, forming red-green or blue-orange pairs.
About two dozen individual nucleotides float in the background.

Figure 3: Beginning at the primer sequence, DNA polymerase (shown in blue) attaches to the original
DNA strand and begins assembling a new, complementary strand.

After the primer is in place on a single, unwound polynucleotide strand, DNA polymerase wraps itself
around that strand, and it attaches new nucleotides to the exposed nitrogenous bases. In this way, the
polymerase assembles a new DNA strand on top of the existing one (Figure 3).

A schematic shows two rows of nucleotides. Each individual nucleotide is represented as an elongated,
vertical, colored rectangle (a nitrogenous base) bound at one end to a grey horizontal cylinder (a sugar
molecule). Each nitrogenous base binds specifically to its partner, with A and T forming a pair and C and
G forming a pair.

Figure 4: Each nucleotide has an affinity for its partner. A pairs with T, and C pairs with G.

Figure Detail

As DNA polymerase makes its way down the unwound DNA strand, it relies upon the pool of free-
floating nucleotides surrounding the existing strand to build the new strand. The nucleotides that make
up the new strand are paired with partner nucleotides in the template strand; because of their
molecular structures, A and T nucleotides always pair with one another, and C and G nucleotides always
pair with one another. This phenomenon is known as complementary base pairing (Figure 4), and it
results in the production of two complementary strands of DNA.

A schematic shows a region of DNA, with part of the DNA being single-stranded and most of the DNA
being double-stranded. A transparent blue globular structure, representing the enzyme DNA
polymerase, is bound to a several-nucleotide-long region along the DNA strand about a quarter of the
way from the left side. The DNA is single-stranded to the left of DNA polymerase and double stranded to
the right, indicating that DNA polymerase is moving from right to left as it replicates the DNA strand. The
sugar-phosphate backbone is depicted as a segmented grey cylinder. Nitrogenous bases are represented
by blue, orange, red, or green vertical rectangles attached above each segment of the sugar-phosphate
backbone. The region of DNA bound by DNA polymerase is visible inside the transparent enzyme at a
higher magnification. Six nucleotides in this region are bound to six complementary nucleotides
arranged above and in parallel to the single strand, forming red-green or blue-orange pairs of rungs
between the grey cylinders. About a half dozen individual nucleotides float in the background.

Figure 5: A new DNA strand is synthesized. This strand contains nucleotides that are complementary to
those in the template sequence.

Base pairing ensures that the sequence of nucleotides in the existing template strand is exactly matched
to a complementary sequence in the new strand, also known as the anti-sequence of the template
strand. Later, when the new strand is itself copied, its complementary strand will contain the same
sequence as the original template strand. Thus, as a result of complementary base pairing, the
replication process proceeds as a series of sequence and anti-sequence copying that preserves the
coding of the original DNA.