Jove
Visualize
Contact Us

Related Concept Videos

Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.7K
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...
6.7K
Size and Structure of Viral Genomes01:26

Size and Structure of Viral Genomes

704
Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
704
Retroviruses02:33

Retroviruses

14.6K
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’...
14.6K
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

49.3K
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...
49.3K
Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

2.1K
Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
2.1K
Mechanisms of Retrovirus-induced Cancers01:51

Mechanisms of Retrovirus-induced Cancers

6.9K
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...
6.9K

You might also read

Related Articles

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

Sort by
Same author

Alternative splicing in the RBMXL1 5'-UTR induces uORF-mediated translation control in activated B lymphocytes.

Scientific reports·2025
Same author

Understanding the role of tRNA modifications in UGA recoding as selenocysteine in eukaryotes.

Journal of molecular biology·2025
Same author

Non-AUG HIV-1 uORF translation elicits specific T cell immune response and regulates viral transcript expression.

Nature communications·2025
Same author

Delivery of Prime editing in human stem cells using pseudoviral NanoScribes particles.

Nature communications·2025
Same author

Selenium Discrepancies in Fetal Bovine Serum: Impact on Cellular Selenoprotein Expression.

International journal of molecular sciences·2024
Same author

Aflatoxin B1 and Epstein-Barr virus-induced CCL22 expression stimulates B cell infection.

Proceedings of the National Academy of Sciences of the United States of America·2024
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: Jan 18, 2026

Designing, Packaging, and Delivery of High Titer CRISPR Retro and Lentiviruses via Stereotaxic Injection
11:28

Designing, Packaging, and Delivery of High Titer CRISPR Retro and Lentiviruses via Stereotaxic Injection

Published on: May 23, 2016

18.3K

[Harnessing retroviral engineering for genome reprogramming].

Philippe-Emmanuel Mangeot1, Théophile Ohlmann1

  • 1CIRI, Centre international de recherche en infectiologie Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, Lyon, France.

Medecine Sciences : M/S
|September 8, 2025
PubMed
Summary

Retroviral vectorology utilizes lentiviral vectors for gene delivery. Emerging defective retroviral particles offer transient delivery of genome-editing tools like CRISPR Cas9, addressing key challenges in genetic engineering.

More Related Videos

Non-Viral Engineering of Primary Human T Cells via Homology-Mediated End-Joining Targeted Integration of Large DNA Templates
06:10

Non-Viral Engineering of Primary Human T Cells via Homology-Mediated End-Joining Targeted Integration of Large DNA Templates

Published on: May 9, 2025

906
Interview: HIV-1 Proviral DNA Excision Using an Evolved Recombinase
10:20

Interview: HIV-1 Proviral DNA Excision Using an Evolved Recombinase

Published on: June 16, 2008

11.8K

Related Experiment Videos

Last Updated: Jan 18, 2026

Designing, Packaging, and Delivery of High Titer CRISPR Retro and Lentiviruses via Stereotaxic Injection
11:28

Designing, Packaging, and Delivery of High Titer CRISPR Retro and Lentiviruses via Stereotaxic Injection

Published on: May 23, 2016

18.3K
Non-Viral Engineering of Primary Human T Cells via Homology-Mediated End-Joining Targeted Integration of Large DNA Templates
06:10

Non-Viral Engineering of Primary Human T Cells via Homology-Mediated End-Joining Targeted Integration of Large DNA Templates

Published on: May 9, 2025

906
Interview: HIV-1 Proviral DNA Excision Using an Evolved Recombinase
10:20

Interview: HIV-1 Proviral DNA Excision Using an Evolved Recombinase

Published on: June 16, 2008

11.8K

Area of Science:

  • Molecular Biology
  • Virology
  • Biotechnology

Background:

  • Advances in HIV-1 biology have spurred the development of retroviral vectorology.
  • Lentiviral vectors are widely used tools in laboratories for gene delivery applications.

Purpose of the Study:

  • To review major retroviral systems employed for genome manipulation.
  • To explore the evolution and application of genome engineering technologies.

Main Methods:

  • Analysis of retroviral assembly and integration mechanisms.
  • Overview of CRISPR-Cas9 and its derivatives for precise genome modification.
  • Discussion of defective retroviral particles for transient effector delivery.

Main Results:

  • Retroviral vectorology has evolved significantly, offering diverse tools for genetic manipulation.
  • Defective retroviral particles show promise for transient delivery of genome editors.
  • CRISPR-Cas9 systems enable high-precision genome editing.

Conclusions:

  • Retroviral systems are crucial for advancing genome engineering.
  • Overcoming challenges in effector delivery is key for effective genome manipulation.
  • The field continues to develop innovative tools for precise genetic modification.