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

RNA Interference01:23

RNA Interference

RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
Homologous Recombination02:31

Homologous Recombination

The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
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...
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
siRNA - Small Interfering RNAs02:30

siRNA - Small Interfering RNAs

Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the ATP-dependent...
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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...

You might also read

Related Articles

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

Sort by
Same author

Identifying Key Questions and Challenges in Microchimerism Biology.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2025
Same author

What's In a Name? Beyond Binaries of Sex and Gender.

Archives of sexual behavior·2025
Same author

Subjective and objective corruption of intuition and rational choice.

The Behavioral and brain sciences·2024
Same author

Germline ecology: Managed herds, tolerated flocks, and pest control.

The Journal of heredity·2024
Same author

On the Origins of Gender Identity.

Archives of sexual behavior·2023
Same author

Paradox lost: Concerted evolution and centromeric instability: Centromeres are hospitable habitats for repeats that evolve adaptations for proliferation within the nucleus sometimes at organismal cost.: Centromeres are hospitable habitats for repeats that evolve adaptations for proliferation within the nucleus sometimes at organismal cost.

BioEssays : news and reviews in molecular, cellular and developmental biology·2022

Related Experiment Video

Updated: Jun 19, 2026

Determination of Self-(In)compatibility and Inter-(In)compatibility Relationships in Citrus Using Manual Pollination, Microscopy, and S-Genotype Analyses
07:12

Determination of Self-(In)compatibility and Inter-(In)compatibility Relationships in Citrus Using Manual Pollination, Microscopy, and S-Genotype Analyses

Published on: June 30, 2023

Collective enforcement of S-RNase-based self-incompatibility.

David Haig1

  • 1Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, 02138, USA.

The New Phytologist
|June 18, 2026
PubMed
Summary

This study models how new nonself-incompatibilities arise, driven by natural selection favoring S-RNase mutations that benefit self-incompatible (SI) over self-compatible (SC) plants. This dynamic shapes plant reproductive strategies.

Keywords:
SLFS‐RNasesegregation distortionself‐compatibilityself‐incompatibility

More Related Videos

Determination of Self- and Inter-(in)compatibility Relationships in Apricot Combining Hand-Pollination, Microscopy and Genetic Analyses
08:08

Determination of Self- and Inter-(in)compatibility Relationships in Apricot Combining Hand-Pollination, Microscopy and Genetic Analyses

Published on: June 16, 2020

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
07:55

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

Published on: September 11, 2022

Related Experiment Videos

Last Updated: Jun 19, 2026

Determination of Self-(In)compatibility and Inter-(In)compatibility Relationships in Citrus Using Manual Pollination, Microscopy, and S-Genotype Analyses
07:12

Determination of Self-(In)compatibility and Inter-(In)compatibility Relationships in Citrus Using Manual Pollination, Microscopy, and S-Genotype Analyses

Published on: June 30, 2023

Determination of Self- and Inter-(in)compatibility Relationships in Apricot Combining Hand-Pollination, Microscopy and Genetic Analyses
08:08

Determination of Self- and Inter-(in)compatibility Relationships in Apricot Combining Hand-Pollination, Microscopy and Genetic Analyses

Published on: June 16, 2020

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
07:55

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

Published on: September 11, 2022

Area of Science:

  • Evolutionary biology
  • Plant reproductive genetics
  • Molecular evolution

Background:

  • Previous models focused on the evolution of self-incompatibilities.
  • The origin of nonself-incompatibilities, crucial for understanding mating system evolution, remains less explored.
  • Self-incompatibility (SI) and self-compatibility (SC) systems significantly impact plant population genetics and evolution.

Purpose of the Study:

  • To present a novel model explaining the evolutionary origin of new nonself-incompatibilities.
  • To investigate the interplay between S-RNase mutations and SLF repertoire evolution in shaping mating system dynamics.
  • To elucidate the selective pressures driving the balance between SI and SC haplotypes.

Main Methods:

  • Theoretical modeling of evolutionary dynamics.
  • Analysis of selection pressures on S-RNase and SLF genes.
  • Simulation of haplotype frequency changes under different evolutionary scenarios.

Main Results:

  • Natural selection favors S-RNase mutations that create nonself-incompatibilities with SC haplotypes, allowing SI haplotypes to avoid inbreeding costs.
  • The generation of nonself-incompatibilities is counteracted by selection on SLF repertoires, promoting compatibility.
  • The model predicts a dynamic balance between forces favoring new compatibilities and those generating new nonself-incompatibilities.

Conclusions:

  • The evolution of mating systems is driven by a fluctuating balance between selection for new compatibilities and 'mutational adjustment' of S-RNases.
  • This balance determines the relative frequencies of SI and SC haplotypes over evolutionary time.
  • The model provides a framework for understanding the maintenance and breakdown of self-incompatibility.