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Related Concept Videos

Herpes01:28

Herpes

Herpes simplex type 1 (HSV‑1) is a widespread pathogen responsible for orolabial lesions. It is an enveloped, double-stranded DNA (dsDNA) virus belonging to the family Herpesviridae. Once the virus infects a host cell, its double‑stranded DNA genome is delivered into the nucleus, where a coordinated cascade of immediate‑early, early, and late gene expression directs viral DNA replication, structural protein synthesis, and virion assembly. After primary infection of epithelial cells, HSV-1...
DNA Replication02:40

DNA Replication

DNA replication involves the separation of the two strands of the double helix, with each strand serving as a template from which the new complementary strand is copied.  After replication, each double-stranded DNA includes one parental or “old” strand and one “new” strand. This is known as semiconservative replication. The resulting DNA molecules have the same sequence and are divided equally into the two daughter cells.
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Translesion DNA Polymerases02:10

Translesion DNA Polymerases

Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
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Size and Structure of Viral Genomes01:26

Size and Structure of Viral Genomes

Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
Prokaryotic DNA Replication01:32

Prokaryotic DNA Replication

DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the single origin of replication (ori) on the cell's circular chromosome. Replication then proceeds around the entire circle of the chromosome in each direction from the two replication forks, resulting in two DNA molecules.
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The DNA Replication Fork01:02

The DNA Replication Fork

An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication forks, one in...

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Related Experiment Video

Updated: Jul 3, 2026

Purification of Viral DNA for the Identification of Associated Viral and Cellular Proteins
08:26

Purification of Viral DNA for the Identification of Associated Viral and Cellular Proteins

Published on: August 31, 2017

Studies on a temperature-sensitive step essential to herpesvirus DNA replication.

J G Stevens1, N L Jackson

  • 1UCLA School of Medicine, Department of Medical Microbiology and Immunology, Los Angeles, California 90024, USA.

Virology
|August 1, 1967
PubMed
Summary

Investigating infectious bovine rhinotracheitis virus replication, a heat-sensitive step occurs one hour post-infection. This step likely involves changes to the viral deoxyribonucleic acid (DNA) or its location, influenced by increased DNA polymerase activity.

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Area of Science:

  • Virology
  • Molecular Biology
  • Biochemistry

Background:

  • Infectious bovine rhinotracheitis virus (IBRV) replication involves a critical heat-sensitive step.
  • Previous research (Stevens, 1966) identified this essential step.

Purpose of the Study:

  • To investigate the precise nature and timing of the heat-sensitive step in IBRV deoxyribonucleic acid (DNA) replication.
  • To understand the role of DNA polymerase activity in this process.

Main Methods:

  • Utilizing temperature "shift down" experiments to pinpoint the timing of the heat-sensitive step.
  • Measuring viral DNA polymerase activity at different temperatures (37°C and 42°C).

Main Results:

  • The heat-sensitive step was determined to occur approximately 1 hour after infection.
  • IBRV infection led to increased activity of a unique viral DNA polymerase at both 37°C and 42°C.

Conclusions:

  • The heat-sensitive step is crucial for IBRV DNA replication.
  • This step likely involves a modification in the intracellular location or physical state of the infecting viral DNA.
  • Elevated DNA polymerase activity supports the proposed mechanism.