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

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.
Bioreactor Controls-III01:22

Bioreactor Controls-III

Strain improvement is a foundational strategy in industrial microbiology aimed at maximizing microbial productivity, particularly because natural isolates typically yield commercially valuable products in very low concentrations. Although optimizing the culture medium and environmental conditions can improve yields, these adjustments are inherently limited by the organism’s genetic potential. As a result, the focus shifts toward genetic modifications to enhance biosynthetic capacity. The...

You might also read

Related Articles

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

Sort by
Same author

Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium.

Genome biology·2020
Same author

Multispecific Antibody Development Platform Based on Human Heavy Chain Antibodies.

Frontiers in immunology·2019
Same author

Stroke in patients with cardiovascular implantable electronic device infection undergoing transvenous lead removal.

Heart rhythm·2019
Same author

Incidence, patterns, and outcomes after transvenous cardiac device lead macrodislodgment: Insights from a population-based study.

Heart rhythm·2018
Same author

Outcomes of video-assisted thoracoscopic surgery for transvenous lead extraction.

Journal of cardiovascular electrophysiology·2018
Same author

Strategies to Obtain Diverse and Specific Human Monoclonal Antibodies From Transgenic Animals.

Transplantation·2017

Related Experiment Video

Updated: Jul 13, 2026

The Green Monster Process for the Generation of Yeast Strains Carrying Multiple Gene Deletions
13:06

The Green Monster Process for the Generation of Yeast Strains Carrying Multiple Gene Deletions

Published on: December 15, 2012

Rescuing yeast mutants with human genes.

Michael J Osborn1, J Ross Miller

  • 1The Babraham Institute, Cambridge CB2 4AT, UK.

Briefings in Functional Genomics & Proteomics
|August 19, 2007
PubMed
Summary

Yeast gene complementation allows researchers to identify human genes with similar functions. This powerful technique has successfully uncovered genes involved in crucial processes like apoptosis and steroid signaling.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Schizosaccharomyces pombe and Saccharomyces cerevisiae are well-established model organisms.
  • These yeasts have been used for decades to isolate genes from other species.
  • Gene isolation is often achieved through complementation of yeast mutations using heterologous cDNA libraries.

Purpose of the Study:

  • To highlight the utility of yeast gene complementation as a tool for functional genomics.
  • To demonstrate the successful application of yeast complementation in identifying human genes.
  • To showcase the use of yeast systems for studying conserved biological pathways like apoptosis and steroid receptor signaling.

Main Methods:

  • Utilizing mutations in fission yeast (Schizosaccharomyces pombe) and budding yeast (Saccharomyces cerevisiae) that confer growth defects.

More Related Videos

Genetic Studies of Human DNA Repair Proteins Using Yeast as a Model System
14:09

Genetic Studies of Human DNA Repair Proteins Using Yeast as a Model System

Published on: March 18, 2010

Genetic Engineering of an Unconventional Yeast for Renewable Biofuel and Biochemical Production
10:10

Genetic Engineering of an Unconventional Yeast for Renewable Biofuel and Biochemical Production

Published on: September 20, 2016

Related Experiment Videos

Last Updated: Jul 13, 2026

The Green Monster Process for the Generation of Yeast Strains Carrying Multiple Gene Deletions
13:06

The Green Monster Process for the Generation of Yeast Strains Carrying Multiple Gene Deletions

Published on: December 15, 2012

Genetic Studies of Human DNA Repair Proteins Using Yeast as a Model System
14:09

Genetic Studies of Human DNA Repair Proteins Using Yeast as a Model System

Published on: March 18, 2010

Genetic Engineering of an Unconventional Yeast for Renewable Biofuel and Biochemical Production
10:10

Genetic Engineering of an Unconventional Yeast for Renewable Biofuel and Biochemical Production

Published on: September 20, 2016

  • Complementation of these yeast mutations by expressing cDNA libraries from heterologous organisms, primarily human.
  • Deducing gene function based on the successful complementation of specific yeast mutations by human genes.
  • Main Results:

    • Successful identification of human genes with conserved functions by complementing yeast mutations.
    • Demonstrated efficacy of yeast complementation in fields seemingly unrelated to yeast biology, such as apoptosis and steroid receptor signaling.
    • Established yeast as a versatile platform for functional gene discovery across diverse biological processes.

    Conclusions:

    • Yeast gene complementation is a robust and widely applicable method for discovering gene functions.
    • This technique facilitates the identification of evolutionarily conserved pathways and molecular mechanisms.
    • The study underscores the power of model organisms in unraveling complex biological processes in higher eukaryotes.