Jove
Visualize
Contact Us

Related Concept Videos

The Replisome03:01

The Replisome

34.7K
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
34.7K
Chromosome Replication02:31

Chromosome Replication

9.1K
Before a cell can divide, it must accurately replicate all of its chromosomes, including the DNA and its associated histone and non-histone proteins.  This process begins at numerous origins of replication during the S phase of the cell cycle in each of a cell’s chromosomes simultaneously. Certain nucleotides can act as origins of replication, but these sequences are not well defined - especially in complex, multi-cellular, eukaryotic species. The length of DNA that spans an origin...
9.1K
Exon Recombination02:32

Exon Recombination

3.7K
The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
Exon shuffling follows “splice frame rules.” Each exon...
3.7K
Gene Duplication and Divergence02:37

Gene Duplication and Divergence

6.3K
The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are...
6.3K
Duplication of Chromatin Structure02:05

Duplication of Chromatin Structure

5.8K
The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...
5.8K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.1K
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...
6.1K

You might also read

Related Articles

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

Sort by
Same author

A yeast recombination system recapitulates the length polymorphism of a microsatellite implicated in human social behavior.

NAR molecular medicine·2026
Same author

RNAs anchoring replication complex control initiation and firing of DNA replication.

Nature communications·2026
Same author

Inherent instability of simple DNA repeats shapes an evolutionarily stable distribution of repeat lengths.

Nature communications·2025
Same author

The origin of mirror repeats in the human genome.

Nucleic acids research·2025
Same author

Whole-brain chemosensory responses of both <i>C. elegans</i> sexes.

bioRxiv : the preprint server for biology·2025
Same author

RNAs anchoring replication complex control initiation and firing of DNA replication.

Research square·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: Sep 11, 2025

Author Spotlight: Characterizing DNA Replication of Pathogenic Repeats to Uncover Mechanisms of Replication Fork Stalling and Expansion
05:22

Author Spotlight: Characterizing DNA Replication of Pathogenic Repeats to Uncover Mechanisms of Replication Fork Stalling and Expansion

Published on: September 13, 2024

878

Emerging drivers of DNA repeat expansions.

Liangzi Li1, W Shem Scott1, Sergei M Mirkin1

  • 1Department of Biology, Tufts University, Medford, MA 02155, U.S.A.

Biochemical Society Transactions
|August 13, 2025
PubMed
Summary
This summary is machine-generated.

Short tandem repeat (STR) expansions cause repeat expansion diseases (REDs), often affecting the nervous system. Recent studies suggest DNA single-strand breaks drive large-scale STR instability, with the FANCD2/FANCI nuclease being a key genetic modifier.

Keywords:
genome editingrepeat contractionsrepeat expansion diseasesrepeat expansions

More Related Videos

Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions
10:16

Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions

Published on: June 28, 2018

32.7K
Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
08:53

Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method

Published on: May 2, 2025

482

Related Experiment Videos

Last Updated: Sep 11, 2025

Author Spotlight: Characterizing DNA Replication of Pathogenic Repeats to Uncover Mechanisms of Replication Fork Stalling and Expansion
05:22

Author Spotlight: Characterizing DNA Replication of Pathogenic Repeats to Uncover Mechanisms of Replication Fork Stalling and Expansion

Published on: September 13, 2024

878
Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions
10:16

Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions

Published on: June 28, 2018

32.7K
Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
08:53

Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method

Published on: May 2, 2025

482

Area of Science:

  • Genetics
  • Molecular Biology
  • Neuroscience

Background:

  • Short tandem repeat (STR) expansions are linked to hereditary repeat expansion diseases (REDs).
  • REDs encompass neurodegenerative and neurodevelopmental disorders like Huntington's disease and Fragile X syndrome.
  • STR expansions are also implicated in common neurodegenerative conditions such as Alzheimer's and Parkinson's disease.

Purpose of the Study:

  • To review recent findings on the mechanisms driving STR instability.
  • To explore the role of DNA single-strand breaks in large-scale STR expansions.
  • To highlight key genetic modifiers of REDs.

Main Methods:

  • Literature review of recent studies on STR instability.
  • Analysis of evidence supporting DNA single-strand breaks as drivers of instability.
  • Examination of the role of specific proteins in REDs pathogenesis.

Main Results:

  • DNA single-strand breaks are proposed as significant drivers of large-scale STR instability.
  • This instability occurs in both dividing and non-dividing cells.
  • The FANCD2- and FANCI-associated nuclease 1 (FAN1) is identified as a potent genetic modifier of REDs.

Conclusions:

  • DNA single-strand breaks represent a critical mechanism underlying STR instability and REDs.
  • Understanding these mechanisms can inform therapeutic strategies for neurodegenerative disorders.
  • Targeting key proteins like FAN1 may offer new avenues for treating repeat expansion diseases.