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Related Concept Videos

Chromosome Replication02:31

Chromosome Replication

Before a cell can divide, it must accurately replicate all of its chromosomes, including the DNA and its associated histone and non-histone proteins.  This process begins at numerous origins of replication during the S phase of the cell cycle in each of a cell’s chromosomes simultaneously. Certain nucleotides can act as origins of replication, but these sequences are not well defined - especially in complex, multi-cellular, eukaryotic species. The length of DNA that spans an origin of...
Viruses with RNA Genomes01:29

Viruses with RNA Genomes

RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart, a...
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...
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...
Replication in Eukaryotes01:29

Replication in Eukaryotes

In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
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Related Experiment Video

Updated: May 23, 2026

Isolation of Viral Replication Compartment-enriched Sub-nuclear Fractions from Adenovirus-infected Normal Human Cells
10:22

Isolation of Viral Replication Compartment-enriched Sub-nuclear Fractions from Adenovirus-infected Normal Human Cells

Published on: November 12, 2015

Replication-uncoupled histone deposition during adenovirus DNA replication.

Tetsuro Komatsu1, Kyosuke Nagata

  • 1Department of Infection Biology, Faculty of Medicine and Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.

Journal of Virology
|April 13, 2012
PubMed
Summary

Viral DNA in infected cells associates with histones during both early and late infection stages. Histone variant H3.3 is selectively bound, suggesting replication-uncoupled histone deposition.

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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

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Last Updated: May 23, 2026

Isolation of Viral Replication Compartment-enriched Sub-nuclear Fractions from Adenovirus-infected Normal Human Cells
10:22

Isolation of Viral Replication Compartment-enriched Sub-nuclear Fractions from Adenovirus-infected Normal Human Cells

Published on: November 12, 2015

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

Area of Science:

  • Molecular Biology
  • Virology
  • Epigenetics

Background:

  • Chromatin structure of adenovirus DNA is crucial for genome functions in infected cells.
  • Incoming viral DNA associates with viral protein VII and histones in early infection phases.

Purpose of the Study:

  • To investigate histone association with newly synthesized viral DNA in late infection phases.
  • To explore the role of histone chaperones and DNA binding proteins in viral chromatin formation.

Main Methods:

  • Chromatin immunoprecipitation assays with epitope-tagged histone H3.
  • Microscopic analyses of histone and transcription factor localization.
  • Knockdown of CAF-1 (chromatin assembly factor-1) and observation of its effect on histone binding.

Main Results:

  • Newly synthesized adenovirus DNA associates with histones in late infection.
  • Histone variant H3.3 is selectively bound to both incoming and newly synthesized viral DNA.
  • CAF-1 knockdown does not alter histone H3 levels on viral chromatin, despite CAF-1 accumulation at replication foci.
  • Histones, but not USF1, are excluded from viral DNA replication foci, mediated by DNA binding protein (DBP) oligomerization.

Conclusions:

  • Histone deposition onto newly synthesized viral DNA appears uncoupled from viral DNA replication.
  • DBP oligomerization may play a role in this replication-uncoupled histone deposition process.