Related Experiment Video
Updated: Jun 23, 2026

07:16
Reverse Genetic Approach to Identify Regulators of Pigmentation using Zebrafish
Published on: March 1, 2022
Chemical genomics identifies compounds affecting Xenopus laevis pigment cell development
Matthew L Tomlinson1, Martin Rejzek, Mark Fidock
1School of Biological Sciences, University of East Anglia, Norwich NR47TJ, UK. grant.wheeler@uea.ac.uk
Molecular Biosystems
|April 28, 2009
Summary
Researchers screened Xenopus laevis embryos to find chemicals impacting pigmented cell development. This screen identified compounds affecting cell migration, morphology, and pigmentation, offering new molecular tools and potential therapeutic leads.
Area of Science:
- Developmental Biology
- Chemical Genomics
- Toxicology
Background:
- Pigmented cell development is crucial for various biological functions, including vision and camouflage.
- Xenopus laevis embryos provide a versatile model system for studying early development and toxicology.
- Chemical genomic screens are powerful tools for identifying bioactive compounds and their molecular targets.
Purpose of the Study:
- To identify novel chemical compounds that disrupt pigmented cell development in Xenopus laevis embryos.
- To investigate the effects of identified compounds on cell migration, morphology, and pigmentation.
- To explore potential molecular targets and therapeutic applications of these compounds.
Main Methods:
- A forward chemical genomic screen using Xenopus laevis embryos.
- Observation of phenotypes related to cell migration, morphology, and pigmentation.
- Utilisation of Xenopus melanophore and human melanoma cell lines for follow-up assays.
- Identification of molecular targets for selected compounds.
Main Results:
- Identification of compounds affecting retinal pigment epithelial (RPE) and melanophore development.
- Observed phenotypes included altered cell migration, morphology, and pigmentation.
- Compounds also impacted general patterning, morphogenesis, eye development, and edema formation.
- Molecular targets for three compounds were elucidated.
Conclusions:
- Chemical genomic screening in Xenopus is effective for discovering compounds that affect pigmented cell development.
- The identified compounds serve as valuable molecular tools and provide biological insights.
- This approach can lead to the discovery of new protein targets and potential therapeutic agents for pigmentary disorders and other conditions.
Related Concept Videos
Reporter Genes
Reporter genes are a type of protein-coding gene that are often tagged to a gene of interest. Once inside a target cell, reporter genes usually produce visually identifiable characteristics like fluorescence and luminescence when expressed along with the gene of interest. Thus, reporter genes “report” the presence or absence of genes of interest in an organism, determine the gene expression pattern, or track the physical location of a DNA segment or protein in the cell.
Commonly used reporter...
Commonly used reporter...
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...
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...
Pharmacogenomics: Identification of New Drug Targets
Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...

