Jove
Visualize
Contact Us

Related Concept Videos

DNA-only Transposons02:57

DNA-only Transposons

14.5K
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...
14.5K
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

11.5K
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...
11.5K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.0K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
6.0K
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

13.9K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
13.9K
Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

15.5K
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...
15.5K
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

6.9K
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...
6.9K

You might also read

Related Articles

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

Sort by
Same author

Comprehensive Lineage Tracing Maps the Landscape of Cell Fate Decisions in Mouse Embryogenesis.

bioRxiv : the preprint server for biology·2026
Same author

Nuclear speckles enable processing of RNA from GC-rich isochores.

Cell·2026
Same author

Fertilization with Protamine-2 deficient sperm triggers abnormal pronucleus development and zygotic cleavage†.

Biology of reproduction·2026
Same author

Lamin A/C directs nucleosome-scale chromatin remodeling to define early lineage segregation in mammals.

bioRxiv : the preprint server for biology·2026
Same author

Acquisition of ampliconic sequences marks a selfish mouse t-haplotype.

Nature communications·2025
Same author

Conditional ATXN2L-Null in Adult Frontal Cortex CamK2a+ Neurons Does Not Cause Cell Death but Restricts Spontaneous Mobility and Affects the Alternative Splicing Pathway.

Cells·2025
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 Experiment Video

Updated: Jul 3, 2025

In vivo Application of the REMOTE-control System for the Manipulation of Endogenous Gene Expression
08:54

In vivo Application of the REMOTE-control System for the Manipulation of Endogenous Gene Expression

Published on: March 29, 2019

7.1K

Autonomous transposons tune their sequences to ensure somatic suppression.

İbrahim Avşar Ilık1, Petar Glažar1, Kevin Tse2

  • 1Otto Warburg Laboratories, Max Planck Institute for Molecular Genetics, Berlin, Germany.

Nature
|February 14, 2024
PubMed
Summary

SAFB proteins prevent transposable elements (TEs) from integrating into the genome and maintain splicing integrity by suppressing TE exonization. This RNA-based defense complements germline pathways, protecting somatic cells from TEs.

More Related Videos

Transposon Mediated Integration of Plasmid DNA into the Subventricular Zone of Neonatal Mice to Generate Novel Models of Glioblastoma
10:58

Transposon Mediated Integration of Plasmid DNA into the Subventricular Zone of Neonatal Mice to Generate Novel Models of Glioblastoma

Published on: February 22, 2015

12.9K
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

10.4K

Related Experiment Videos

Last Updated: Jul 3, 2025

In vivo Application of the REMOTE-control System for the Manipulation of Endogenous Gene Expression
08:54

In vivo Application of the REMOTE-control System for the Manipulation of Endogenous Gene Expression

Published on: March 29, 2019

7.1K
Transposon Mediated Integration of Plasmid DNA into the Subventricular Zone of Neonatal Mice to Generate Novel Models of Glioblastoma
10:58

Transposon Mediated Integration of Plasmid DNA into the Subventricular Zone of Neonatal Mice to Generate Novel Models of Glioblastoma

Published on: February 22, 2015

12.9K
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

10.4K

Area of Science:

  • Genetics
  • Molecular Biology
  • Epigenetics

Background:

  • Transposable elements (TEs) occupy significant portions of genomes, including human introns.
  • While transcribed, TEs are typically spliced out and degraded, but can cause splicing errors like exonization.
  • A robust splicing code normally prevents TE exonization, but the mechanisms are not fully understood.

Purpose of the Study:

  • To investigate the role of SAFB proteins in genome integrity and splicing.
  • To understand how SAFB proteins prevent transposable element (TE) exonization.
  • To elucidate the broader suppressive activity of SAFB proteins on various repetitive elements.

Main Methods:

  • Investigated SAFB protein binding to L1 element sequences.
  • Assessed SAFB's impact on splicing of introns containing TEs.
  • Examined SAFB's suppressive effects on different types of TEs and genomic elements.
  • Compared SAFB expression and activity in somatic cells versus germline cells (testis).

Main Results:

  • SAFB proteins bind to adenosine-rich sequences in L1 elements, preventing retrotransposition and TE exonization.
  • SAFB's suppressive function extends to cassette exons, nested genes, DNA transposons, and active LTR/ERV elements.
  • Splicing events suppressed by SAFB in somatic cells are reactivated in the testis, correlating with low SAFB levels in spermatids.
  • SAFB acts as an RNA-based defense system in the soma, distinct from the germline's Piwi-interacting RNA pathway.

Conclusions:

  • SAFB proteins play a critical dual role in safeguarding genome integrity by inhibiting TE activity and maintaining splicing fidelity.
  • SAFB's mechanism involves direct binding to conserved TE sequences, highlighting a pattern-guided defense strategy.
  • SAFB represents a somatic, non-adaptive RNA-based defense against TEs, complementing the adaptive germline RNAi pathways.