Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Viral Mutations00:36

Viral Mutations

39.5K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
39.5K
Leaky Scanning02:28

Leaky Scanning

5.6K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.6K
Viruses with RNA Genomes01:29

Viruses with RNA Genomes

662
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...
662
Size and Structure of Viral Genomes01:26

Size and Structure of Viral Genomes

591
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...
591
Viral Recombination00:57

Viral Recombination

24.8K
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
24.8K
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

7.9K
The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
7.9K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The purine-rich element-binding protein ChPur-α negatively regulates Hsc70 transcription in Crassostrea hongkongensis.

Cell stress & chaperones·2017
Same author

Improved antitumor effect of ionizing radiation in combination with rapamycin for treating nasopharyngeal carcinoma.

Oncology letters·2017
Same author

Roles of Cells from the Arterial Vessel Wall in Atherosclerosis.

Mediators of inflammation·2017
Same author

Metabolic and microbial signatures in rat hepatocellular carcinoma treated with caffeic acid and chlorogenic acid.

Scientific reports·2017
Same author

Arsenic removal in aqueous solution by a novel Fe-Mn modified biochar composite: Characterization and mechanism.

Ecotoxicology and environmental safety·2017
Same author

Antidiabetic activities of polysaccharides separated from Inonotus obliquus via the modulation of oxidative stress in mice with streptozotocin-induced diabetes.

PloS one·2017

Related Experiment Video

Updated: Jan 3, 2026

In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation
07:24

In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation

Published on: March 27, 2016

9.4K

Dinucleotide evolutionary dynamics in influenza A virus.

Haogao Gu1, Rebecca L Y Fan1, Di Wang2

  • 1School of Public Health, LKS Faculty of Medicine, G/F, Patrick Manson Building (North Wing), 7 Sassoon Road, Pokfulam, Hong Kong.

Virus Evolution
|November 19, 2019
PubMed
Summary

Influenza A virus shows biases in dinucleotide composition, with CpG and UpA under-represented. Temporal analysis reveals decreased CpG frequency in seasonal H1 virus, impacting evolution and codon usage.

Keywords:
codon usagedinucleotide usageevolutioninfluenza

More Related Videos

Affinity Purification of Influenza Virus Ribonucleoprotein Complexes from the Chromatin of Infected Cells
11:20

Affinity Purification of Influenza Virus Ribonucleoprotein Complexes from the Chromatin of Infected Cells

Published on: June 3, 2012

13.4K
Generation of Escape Variants of Neutralizing Influenza Virus Monoclonal Antibodies
07:55

Generation of Escape Variants of Neutralizing Influenza Virus Monoclonal Antibodies

Published on: August 29, 2017

12.2K

Related Experiment Videos

Last Updated: Jan 3, 2026

In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation
07:24

In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation

Published on: March 27, 2016

9.4K
Affinity Purification of Influenza Virus Ribonucleoprotein Complexes from the Chromatin of Infected Cells
11:20

Affinity Purification of Influenza Virus Ribonucleoprotein Complexes from the Chromatin of Infected Cells

Published on: June 3, 2012

13.4K
Generation of Escape Variants of Neutralizing Influenza Virus Monoclonal Antibodies
07:55

Generation of Escape Variants of Neutralizing Influenza Virus Monoclonal Antibodies

Published on: August 29, 2017

12.2K

Area of Science:

  • Virology
  • Genomics
  • Evolutionary Biology

Background:

  • RNA viruses, including influenza A virus, exhibit significant dinucleotide composition biases.
  • Altered CpG usage in influenza mutants leads to attenuation in mammalian models, but the link to codon usage bias and evolutionary changes remains unclear.

Purpose of the Study:

  • Investigate dinucleotide usage patterns across influenza virus segments and groups.
  • Analyze temporal changes in dinucleotide frequency and their relationship with codon usage bias and evolutionary pressures.

Main Methods:

  • Applied a Monte Carlo method to identify under-represented/over-represented dinucleotide motifs in influenza viral sequences.
  • Accounted for biases from codon usage and amino acid sequences.
  • Analyzed temporal variations in dinucleotide frequency, particularly in seasonal H1 virus post-1977.

Main Results:

  • CpG and UpA dinucleotides are under-represented, while UpG and CpA are over-represented across all viral segments.
  • A significant decrease in CpG frequency was observed in specific segments of the seasonal H1 virus after 1977.
  • Silent mutations primarily drive these temporal dinucleotide variations, leading to altered codon usage bias.

Conclusions:

  • Dinucleotide preference directly influences synonymous codon usage bias in influenza viruses.
  • Understanding these dinucleotide dynamics provides insights into the evolutionary history and selection pressures shaping the influenza virus genome.