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

Splicing accuracy varies across human introns, tissues, age and disease.

Nature communications·2025
Same author

Splicing accuracy varies across human introns, tissues and age.

bioRxiv : the preprint server for biology·2023
Same author

Histone chaperone Asf1 is required for histone H3 lysine 56 acetylation, a modification associated with S phase in mitosis and meiosis.

Proceedings of the National Academy of Sciences of the United States of America·2006
Same author

Histone deposition proteins: links between the DNA replication machinery and epigenetic gene silencing.

Cold Spring Harbor symposia on quantitative biology·2005
Same author

Chromatin proteins are determinants of centromere function.

Current topics in microbiology and immunology·2003
Same author

An in vitro-selected RNA-binding site for the KH domain protein PSI acts as a splicing inhibitor element.

RNA (New York, N.Y.)·2001

Related Experiment Video

Updated: Jul 13, 2026

Recombineering Homologous Recombination Constructs in Drosophila
14:23

Recombineering Homologous Recombination Constructs in Drosophila

Published on: July 13, 2013

Drosophila P element transposase recognizes internal P element DNA sequences.

P D Kaufman1, R F Doll, D C Rio

  • 1Whitehead Institute for Biomedical Research, Nine Cambridge Center, Massachusetts 02142.

Cell
|October 20, 1989
PubMed
Summary

Purified Drosophila P element transposase binds specifically to internal DNA sequences, not terminal repeats, influencing transposition. This binding may also affect P element transcription, suggesting other protein factors are involved.

More Related Videos

Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach
11:12

Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach

Published on: September 11, 2017

Embryo Microinjection for Transgenesis in Drosophila
05:32

Embryo Microinjection for Transgenesis in Drosophila

Published on: June 7, 2024

Related Experiment Videos

Last Updated: Jul 13, 2026

Recombineering Homologous Recombination Constructs in Drosophila
14:23

Recombineering Homologous Recombination Constructs in Drosophila

Published on: July 13, 2013

Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach
11:12

Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach

Published on: September 11, 2017

Embryo Microinjection for Transgenesis in Drosophila
05:32

Embryo Microinjection for Transgenesis in Drosophila

Published on: June 7, 2024

Area of Science:

  • Molecular Biology
  • Genetics
  • Drosophila melanogaster research

Background:

  • Drosophila P transposable elements are mobile genetic sequences.
  • The P element transposase protein is essential for P element transposition and excision.

Purpose of the Study:

  • To investigate the DNA binding properties of purified P element transposase.
  • To identify the specific DNA sequences recognized by transposase.
  • To explore the potential impact of transposase binding on P element transcription.

Main Methods:

  • Purification of Drosophila P element transposase.
  • Site-specific DNA binding assays.
  • In vitro transcription assays.

Main Results:

  • Purified P element transposase is a site-specific DNA binding protein.
  • Transposase binds to a 10 bp internal consensus sequence at both ends of P element DNA, not the terminal inverted repeats.
  • The transposase binding site overlaps with sequences critical for P element promoter activity in vitro.
  • Transposase exhibits high non-specific DNA binding affinity.

Conclusions:

  • P element transposase specifically recognizes internal DNA sequences crucial for transposition.
  • Transposase binding may regulate P element transcription, potentially involving other protein factors.
  • The P element transposition process likely requires additional Drosophila protein factors interacting with terminal DNA sequences.