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

Mismatch Repair01:20

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Mismatch Repair01:36

Mismatch Repair

Overview
Incomplete Dominance01:43

Incomplete Dominance

Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
Spontaneous and Induced Mutations01:30

Spontaneous and Induced Mutations

Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).
Genome Copying Errors02:46

Genome Copying Errors

DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger theirĀ  survival. Therefore, the copying errors are checked and repaired at three levels.

You might also read

Related Articles

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

Sort by
Same author

The Phenotypic Landscape of a Circadian Clock.

bioRxiv : the preprint server for biologyĀ·2026
Same author

Use of andexanet alfa: A British Society for Haematology position statement.

British journal of haematologyĀ·2026
Same author

Simple biological controllers drive the evolution of soft modes.

Proceedings of the National Academy of Sciences of the United States of AmericaĀ·2026
Same author

BCAR: A fast and general barcode-sequence mapper for correcting sequencing errors.

bioRxiv : the preprint server for biologyĀ·2026
Same author

Breast cancer survival by stage at diagnosis in countries in transition: A population-based study.

International journal of cancerĀ·2026
Same author

Current gynaecological management of women and girls with bleeding disorders in the United Kingdom: A UKHCDO haemophilia treatment centre survey and evaluation of real-world clinical practice for the British Journal of Haematology.

British journal of haematologyĀ·2025

Related Experiment Video

Updated: Jul 15, 2026

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis
08:46

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis

Published on: August 26, 2020

Elevated basal slippage mutation rates among the Canidae.

Jeffrey Laidlaw1, Yevgeniy Gelfand, Kar-Wai Ng

  • 1Department of Biochemistry, UT Southwestern Medical Center, Dallas, TX 75390, USA.

The Journal of Heredity
|April 18, 2007
PubMed
Summary

Dogs and other carnivores exhibit a genome-wide increase in slippage mutation rates, contributing to rapid evolutionary change and morphological diversity. This heightened mutation rate is a key factor in their adaptability.

More Related Videos

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
06:59

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter

Published on: March 31, 2022

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair
08:15

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair

Published on: October 6, 2014

Related Experiment Videos

Last Updated: Jul 15, 2026

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis
08:46

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis

Published on: August 26, 2020

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
06:59

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter

Published on: March 31, 2022

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair
08:15

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair

Published on: October 6, 2014

Area of Science:

  • Genetics
  • Evolutionary Biology
  • Genomics

Background:

  • Mammalian morphological diversity, exemplified by dogs, is linked to genetic variation, including tandem repeat length changes in developmental genes.
  • Previous studies suggested dogs had fewer repeat interruptions and higher polymorphism than humans, but genome limitations hindered broad conclusions.

Purpose of the Study:

  • To investigate the genome-wide mutation rate in dogs and its evolutionary implications.
  • To determine if elevated slippage mutation rates are specific to dogs or shared among related species.

Main Methods:

  • Whole-genome analyses of human and dog genomes to assess mutation rates.
  • Sequencing of coding repeat regions in 42 species across 10 carnivore clades.

Main Results:

  • Dogs exhibit a genome-wide increase in the basal germ-line slippage mutation rate compared to humans.
  • An elevated genome-wide slippage mutation rate is a derived trait found in diverse wild canids, distinguishing them from other Carnivora.
  • Similar heightened slippage rates were observed in rodents, another diverse and rapidly evolving taxon.

Conclusions:

  • A genome-wide increase in slippage mutation rate may facilitate rapid evolutionary change and diversification in certain taxa.
  • The 'slippery' genome, characterized by enhanced slippage, appears correlated with major evolutionary radiations in mammals.