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Related Concept Videos

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...
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...
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’...
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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...

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Local features determine Ty3 targeting frequency at RNA polymerase III transcription start sites.

Genome research·2019
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Control of yeast retrotransposons mediated through nucleoporin evolution.

PLoS genetics·2018
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Ty3 requires yeast La homologous protein for wild-type frequencies of transposition.

Molecular microbiology·2003
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Mutational analysis of the transcription factor IIIB-DNA target of Ty3 retroelement integration.

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Ty3 integrase is required for initiation of reverse transcription.

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Related Experiment Video

Updated: Jun 5, 2026

Analysis of LINE-1 Retrotransposition at the Single Nucleus Level
11:52

Analysis of LINE-1 Retrotransposition at the Single Nucleus Level

Published on: April 23, 2016

Function of a retrotransposon nucleocapsid protein.

Suzanne B Sandmeyer1, Kristina A Clemens

  • 1Department of Biological Chemistry, School of Medicine, University of California, Irvine, CA USA. sbsandme@uci.edu

RNA Biology
|December 30, 2010
PubMed
Summary

This review examines the Ty3 retrotransposon

Area of Science:

  • Molecular Biology
  • Genetics
  • Virology

Background:

  • Long terminal repeat (LTR) retrotransposons are significant genomic components in eukaryotes.
  • Understanding retrotransposons offers insights into retroviral functions and genome dynamics.
  • The nucleocapsid (NC) protein is crucial for retroviral and retrotransposon replication.

Purpose of the Study:

  • To review the structure and function of the Ty3 retrotransposon's nucleocapsid (NC) protein.
  • To elucidate the roles of Ty3 NC in retroelement assembly and RNA processing.
  • To explore potential interactions of Ty3 NC with host cellular machinery.

Main Methods:

  • Literature review of studies on Ty3 retrotransposon and its NC protein.
  • Analysis of known functions of retroviral NC proteins.

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Nucleocapsid Annealing-Mediated Electrophoresis (NAME) Assay Allows the Rapid Identification of HIV-1 Nucleocapsid Inhibitors

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Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution
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Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution

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Related Experiment Videos

Last Updated: Jun 5, 2026

Analysis of LINE-1 Retrotransposition at the Single Nucleus Level
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Analysis of LINE-1 Retrotransposition at the Single Nucleus Level

Published on: April 23, 2016

Nucleocapsid Annealing-Mediated Electrophoresis (NAME) Assay Allows the Rapid Identification of HIV-1 Nucleocapsid Inhibitors
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Nucleocapsid Annealing-Mediated Electrophoresis (NAME) Assay Allows the Rapid Identification of HIV-1 Nucleocapsid Inhibitors

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Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution
10:53

Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution

Published on: January 16, 2017

  • Speculative integration of Ty3 NC functions with cellular processes like P-body and stress granule dynamics.
  • Main Results:

    • Ty3 NC is essential for forming retroelement assembly sites (retrosomes).
    • Ty3 NC chaperones primer tRNA for dimerization and circularization of Ty3 genomic RNA.
    • Ty3 NC interactions with Gag3 influence virus-like particle condensation.

    Conclusions:

    • Ty3 NC plays multifaceted roles in retrotransposition, including assembly site formation and RNA management.
    • Ty3 NC may coordinate RNA transition from translation to packaging with host factors.
    • Interactions within the Ty3 Gag-NC complex regulate particle formation.