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

Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
DNA-only Transposons02:57

DNA-only Transposons

DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
Transposons01:24

Transposons

Transposons, or "jumping genes," are small mobile genetic elements (MGEs) that range from 700 to 40,000 base pairs in length. They are found in all organisms and can move within the same chromosome or transfer to different chromosomes. In some cases, transposons can also jump between different host DNA molecules, such as plasmids or viruses, contributing to genetic variability.Barbara McClintock first discovered these mobile genetic elements in the 1940s while studying maize genetics, and she...
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...
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...
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...

You might also read

Related Articles

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

Sort by
Same author

Epigenetics and non-coding RNAs in host-endosymbiont interactions: insights from Wolbachia and beyond.

Current opinion in insect science·2025
Same author

Genomic structure and life history variation of isofemale lineages of Myzus persicae with different levels of parasitization by Diaeretiella rapae.

Scientific reports·2025
Same author

Gene and transposable element expression in response to stress in temperate and tropical populations of Drosophila.

Mobile DNA·2025
Same author

Dual-transcriptomics on microdissected cells reveals functional specialisation of symbiont-bearing-cells and contrasted responses to nutritional stress in the cereal weevil.

Microbiome·2025
Same author

Cooperation between symbiotic partners through protein trafficking.

Proceedings of the National Academy of Sciences of the United States of America·2025
Same author

International congress on transposable elements (ICTE 2024) in Saint Malo: breaking down transposon waves and their impact.

Mobile DNA·2024

Related Experiment Video

Updated: May 21, 2026

Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity
04:04

Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity

Published on: January 20, 2023

Transposable elements: not as quiet as a mouse.

Rita Rebollo1, Ying Zhang, Dixie L Mager

  • 1Terry Fox Laboratory, British Columbia Cancer Agency, Vancouver, BC, Canada.

Genome Biology
|June 22, 2012
PubMed
Summary

Nellåker et al. demonstrate significant removal of harmful transposable element variants in 18 mouse strains via negative selection. This study highlights the power of natural selection in maintaining genome integrity.

Area of Science:

  • Genomics
  • Evolutionary Biology
  • Molecular Genetics

Background:

  • Transposable elements (TEs) are mobile genetic sequences that can cause mutations.
  • The accumulation of deleterious TE variants can impact genome stability and organismal health.
  • Understanding the mechanisms that control TE variant load is crucial for evolutionary and genetic studies.

Purpose of the Study:

  • To investigate the role of negative selection in purging deleterious transposable element variants.
  • To quantify the extent of TE variant purging across multiple mouse strains.
  • To assess the impact of selection on TE dynamics in mammalian genomes.

Main Methods:

  • Comparative genomics analysis of 18 diverse mouse strains.
  • Identification and characterization of transposable element variants.

More Related Videos

Loss-of-Function Approach in the Embryonic Chick Retina by Using Tol2 Transposon-Mediated Transgenic Expression of Artificial microRNAs
06:58

Loss-of-Function Approach in the Embryonic Chick Retina by Using Tol2 Transposon-Mediated Transgenic Expression of Artificial microRNAs

Published on: May 18, 2022

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

Related Experiment Videos

Last Updated: May 21, 2026

Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity
04:04

Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity

Published on: January 20, 2023

Loss-of-Function Approach in the Embryonic Chick Retina by Using Tol2 Transposon-Mediated Transgenic Expression of Artificial microRNAs
06:58

Loss-of-Function Approach in the Embryonic Chick Retina by Using Tol2 Transposon-Mediated Transgenic Expression of Artificial microRNAs

Published on: May 18, 2022

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

  • Application of population genetics methods to infer selection pressures.
  • Bioinformatic analysis of whole-genome sequencing data.
  • Main Results:

    • Massive purging of deleterious transposable element variants was observed across all 18 mouse strains.
    • Evidence of strong negative selection acting against potentially harmful TE insertions and mutations.
    • The rate of purging varied among different types of transposable elements.
    • Significant reduction in the frequency of deleterious TE variants compared to neutral expectations.

    Conclusions:

    • Negative selection plays a critical role in removing harmful transposable element variants, maintaining genome integrity.
    • The findings provide insights into the evolutionary forces shaping transposable element populations in mammals.
    • This study underscores the importance of selection in preventing the accumulation of potentially mutagenic genetic elements.