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Related Concept Videos

Exon Recombination02:32

Exon Recombination

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 has three reading...
Gene Conversion02:08

Gene Conversion

Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Genetic Screens02:46

Genetic Screens

Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which result in visible changes...
Position-effect Variegation02:32

Position-effect Variegation

In 1928, a German botanist Emil Heitz observed the moss nuclei with a DNA binding dye. He observed that while some chromatin regions decondense and spread out in the interphase nucleus, others do not. He termed them euchromatin and heterochromatin, respectively. He proposed that the heterochromatin regions reflect a functionally inactive state of the genome. It was later confirmed that heterochromatin is transcriptionally repressed, and euchromatin is transcriptionally active chromatin.
Genomic DNA in Eukaryotes00:58

Genomic DNA in Eukaryotes

Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.

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Related Experiment Video

Updated: Jun 9, 2026

A Reverse Genetic Approach to Test Functional Redundancy During Embryogenesis
06:59

A Reverse Genetic Approach to Test Functional Redundancy During Embryogenesis

Published on: August 11, 2010

Reverse genetics in eukaryotes.

Serge Hardy1, Vincent Legagneux, Yann Audic

  • 1Université de Rennes 1, Université Européenne de Bretagne, Institut Fédératif de Recherche 140, Rennes, France.

Biology of the Cell
|September 4, 2010
PubMed
Summary

Reverse genetics uses four main methods to study gene function by altering gene activity and observing effects. These techniques, including genome editing and mRNA manipulation, aid in deciphering gene roles in the post-genomic era.

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Area of Science:

  • Genetics
  • Molecular Biology

Background:

  • Reverse genetics is crucial for understanding gene function by analyzing phenotypic changes after gene activity modification.
  • Several distinct methodologies exist to achieve targeted gene manipulation.

Purpose of the Study:

  • To review the primary approaches used in reverse genetics.
  • To highlight the applicability of these methods across different model organisms.

Main Methods:

  • Genome alteration techniques: random mutagenesis (chemical/insertional) with screening, and targeted gene modification via homologous recombination (HR).
  • mRNA-based techniques: RNA interference (RNAi) for gene product reduction, and morpholino (MO) antisense oligonucleotides for mRNA modulation.
  • Comparison of method suitability across model species like Drosophila, mice, yeast, Xenopus, and zebrafish.

Main Results:

  • Genome-wide mutant collections are available in multiple species.
  • Specific model organisms are better suited to particular reverse genetics approaches (e.g., HR in mice/yeast, MO in Xenopus/zebrafish).

Conclusions:

  • The diverse reverse genetics approaches provide powerful tools for functional genomics.
  • Availability of comprehensive mutant collections facilitates gene function discovery in the post-genomic era.