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Related Concept Videos

Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...
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...
Mechanisms of Retrovirus-induced Cancers01:51

Mechanisms of Retrovirus-induced Cancers

Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
Mechanisms of Retrovirus-induced Cancers01:51

Mechanisms of Retrovirus-induced Cancers

Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
LTR Retrotransposons03:08

LTR Retrotransposons

LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...

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Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites
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Macroevolution of complex retroviruses.

Aris Katzourakis1, Robert J Gifford, Michael Tristem

  • 1Zoology Department, University of Oxford, Oxford OX1 3PS, UK. aris.katzourakis@zoo.ox.ac.uk

Science (New York, N.Y.)
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Summary
This summary is machine-generated.

Researchers discovered an ancient foamy virus fossil in sloth genomes, revealing over 100 million years of viral codivergence with mammals. This finding sheds light on evolutionary conflict and host-pathogen dynamics.

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Area of Science:

  • Virology
  • Paleogenomics
  • Evolutionary Biology

Background:

  • Endogenous retroviruses (ERVs) provide a genomic fossil record of past viral infections in hosts.
  • Foamy viruses (FVs), a type of complex retrovirus infecting mammals, have been largely absent from this genomic record.
  • Understanding FV evolutionary history is crucial for deciphering host-pathogen interactions.

Purpose of the Study:

  • To investigate the evolutionary history of foamy viruses in mammals.
  • To identify evidence of endogenous foamy viruses in host genomes.
  • To explore the timescale of foamy virus-mammal codivergence and its evolutionary implications.

Main Methods:

  • Genomic analysis of sloth DNA to identify retroviral sequences.
  • Phylogenetic analysis to establish evolutionary relationships between viruses and hosts.
  • Comparative genomics to assess viral genome structure and host immune mechanisms.

Main Results:

  • Discovery of an endogenous foamy virus (enFV) within sloth genomes.
  • Evidence indicates foamy viruses infected mammals over 100 million years ago.
  • Demonstration of codivergence between foamy viruses and mammalian hosts across a geological era.
  • Identification of evolutionary constraints on viral genome structure and the role of macroevolutionary conflict.

Conclusions:

  • Foamy viruses have a deep evolutionary history in mammals, codiverging with hosts for over 100 million years.
  • Endogenous foamy viruses offer insights into long-term host-pathogen evolutionary dynamics.
  • The study highlights the impact of macroevolutionary conflict on viral accessory genes and host innate immunity.