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

Gene Duplication and Divergence02:37

Gene Duplication and Divergence

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 characterized.
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
Gene Families01:57

Gene Families

Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
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 their  survival. Therefore, the copying errors are checked and repaired at three levels.
Genome Size and the Evolution of New Genes03:21

Genome Size and the Evolution of New Genes

While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.

You might also read

Related Articles

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

Sort by
Same author

Expanding the human proteome with microproteins and peptideins.

Nature·2026
Same author

An expanded reference catalog of translated open reading frames for biomedical research.

Nucleic acids research·2026
Same author

De novo genome assembly, inversion detection, and worldwide adaptation on the invasive species Styela plicata.

Scientific reports·2025
Same author

Translon: a single term for translated regions.

Nature methods·2025
Same author

An expanded reference catalog of translated open reading frames for biomedical research.

bioRxiv : the preprint server for biology·2025
Same author

Incipient Range Expansion of Green Turtles in the Mediterranean.

Molecular ecology·2025
Same journal

The life history of recessive deleterious alleles as seen through the eyes of a honey bee (Apis mellifera).

Molecular biology and evolution·2026
Same journal

Severe bottleneck of ancient Homo populations: Insights from computational modeling and relevant fossil evidence.

Molecular biology and evolution·2026
Same journal

Population Epigenetics: Deciphering DNA Methylation Diversity and its Implications for Health, Disease, and Evolution.

Molecular biology and evolution·2026
Same journal

Genomic signature of repeated transitions to diurnality in spiders.

Molecular biology and evolution·2026
Same journal

Phylogenomic blind spots: The limits of UCE and BUSCO loci in the presence of gene flow.

Molecular biology and evolution·2026
Same journal

seqLens: Optimizing Language Models for Genomic Predictions.

Molecular biology and evolution·2026
See all related articles

Related Experiment Video

Updated: May 11, 2026

Following the Dynamics of Structural Variants in Experimentally Evolved Populations
04:52

Following the Dynamics of Structural Variants in Experimentally Evolved Populations

Published on: February 3, 2023

Accelerated evolution after gene duplication: a time-dependent process affecting just one copy.

Cinta Pegueroles1, Steve Laurie, M Mar Albà

  • 1Evolutionary Genomics Group, Research Programme on Biomedical Informatics (GRIB), Hospital del Mar Research Institute (IMIM), Universitat Pompeu Fabra (UPF), Barcelona, Spain.

Molecular Biology and Evolution
|April 30, 2013
PubMed
Summary
This summary is machine-generated.

Gene duplication drives genome evolution, with one copy often accelerating its evolutionary rate due to positive selection. This rate returns to normal within 40.5 million years, supporting neofunctionalization.

Keywords:
adaptive evolutionevolutionary rategene duplicationgene expressionindelspositive selection

More Related Videos

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome
06:40

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome

Published on: March 22, 2018

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
17:14

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization

Published on: December 10, 2012

Related Experiment Videos

Last Updated: May 11, 2026

Following the Dynamics of Structural Variants in Experimentally Evolved Populations
04:52

Following the Dynamics of Structural Variants in Experimentally Evolved Populations

Published on: February 3, 2023

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome
06:40

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome

Published on: March 22, 2018

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
17:14

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization

Published on: December 10, 2012

Area of Science:

  • Evolutionary biology
  • Genomics
  • Molecular evolution

Background:

  • Gene duplication is a key driver of genome evolution, creating redundant gene copies.
  • The evolutionary trajectories and driving forces behind gene duplicate evolution remain incompletely understood.
  • Gene duplicates often exhibit accelerated evolutionary rates, but the roles of positive selection versus genetic drift are debated.

Purpose of the Study:

  • To investigate the evolutionary mechanisms and rates of divergence in rodent gene duplicates.
  • To determine the contribution of positive selection to the evolution of gene copies after duplication.
  • To understand the timescale of evolutionary rate changes and the role of neofunctionalization.

Main Methods:

  • Comparative genomic analysis of rodent genes duplicated before and after the mouse-rat split.
  • Analysis of sequence divergence and evolutionary rates (nonsynonymous/synonymous substitutions).
  • Application of maximum likelihood-based branch-site tests to detect positive selection.
  • Comparison of gene expression patterns between duplicate copies.

Main Results:

  • One daughter copy of duplicated genes shows significantly increased sequence divergence post-duplication.
  • The evolutionary rate of the accelerated copy is, on average, 5-fold higher in the 4-12 million years post-duplication.
  • Positive selection contributes to this rate acceleration, with rates returning to pre-duplication levels by 40.5 million years.
  • Tissue expression patterns of duplicates parallel substitution rate changes, supporting neofunctionalization.

Conclusions:

  • Gene duplication leads to accelerated evolution in one copy, primarily driven by positive selection.
  • Neofunctionalization is a significant factor in the evolution of young gene duplicates.
  • Evolutionary rates of gene duplicates normalize within approximately 40.5 million years, demonstrating a defined evolutionary trajectory.