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...
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...
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...
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...
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...

You might also read

Related Articles

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

Sort by
Same author

Temporary and permanent mutators lacking the mismatch repair system: the enhancement of mutators in cell populations.

Cold Spring Harbor symposia on quantitative biology·2003
Same author

Direct radiation damage is confined to a single polypeptide in rabbit immunoglobulin G.

Biophysical journal·2003
Same author

Development of a cw-laser-based cavity-ringdown sensor aboard a spacecraft for trace air constituents.

Applied physics. B, Lasers and optics·2003
Same author

A prospective, longitudinal diffusion tensor imaging study of brain injury in newborns.

Neurology·2002
Same author

The novel cytotoxic sponge metabolite peloruside A, structurally similar to bryostatin-1, has unique bioactivity independent of protein kinase C.

Anti-cancer drug design·2002
Same author

Revisiting the structural flexibility of the complex p21(ras)-GTP: the catalytic conformation of the molecular switch II.

Proteins·2001

Related Experiment Video

Updated: May 17, 2026

Generating Transgenic Plants with Single-copy Insertions Using BIBAC-GW Binary Vector
12:08

Generating Transgenic Plants with Single-copy Insertions Using BIBAC-GW Binary Vector

Published on: March 28, 2018

The transposon Tn9 generates a 9 bp repeated sequence during integration.

L Johnsrud, M P Calos, J H Miller

    Cell
    |December 1, 1978
    PubMed
    Summary

    Transposon Tn9 integrates into the E. coli lac operon at multiple sites, forming preferred regions. Insertion is linked to a 9 base pair host DNA repeat generated during the process.

    Area of Science:

    • Molecular Biology
    • Genetics
    • Microbiology

    Background:

    • The lac operon in Escherichia coli is a well-studied genetic system for understanding gene regulation.
    • Transposable elements, like transposon Tn9, are mobile DNA sequences that can alter gene function and genome structure.

    Purpose of the Study:

    • To genetically and physically map insertions of the transposon Tn9 within the lac operon of E. coli.
    • To characterize the sequence features associated with Tn9 integration into the host genome.

    Main Methods:

    • Genetic mapping of 70 Tn9 insertions into the lacI and lacZ genes.
    • Restriction mapping to analyze insertion sites.
    • DNA sequencing of three independent Tn9 insertions.

    Main Results:

    More Related Videos

    Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing
    08:19

    Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing

    Published on: July 7, 2020

    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

    Related Experiment Videos

    Last Updated: May 17, 2026

    Generating Transgenic Plants with Single-copy Insertions Using BIBAC-GW Binary Vector
    12:08

    Generating Transgenic Plants with Single-copy Insertions Using BIBAC-GW Binary Vector

    Published on: March 28, 2018

    Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing
    08:19

    Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing

    Published on: July 7, 2020

    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

    • Tn9 demonstrated insertion into at least 50 distinct sites within the lacI and lacZ genes, originating from a common chromosomal point.
    • Analysis revealed preferred insertion regions, characterized by multiple integration points within localized areas.
    • Sequence analysis showed Tn9 integration is associated with a 9 base pair direct repeat of host DNA, generated during insertion.

    Conclusions:

    • Transposon Tn9 exhibits site-specificity in its integration into the E. coli lac operon, with preferred but multiple target sites.
    • The integration mechanism of Tn9 involves the generation of a short direct repeat of host DNA sequence at the insertion junction.