Related Experiment Video
Updated: Jul 10, 2026

05:48
Removal of an Internal Translational Start Site from mRNA While Retaining Expression of the Full-Length Protein
Published on: March 16, 2022
Generation of a Mig-6 conditional null allele.
Nili Jin1, Jennifer L Gilbert, Russell R Broaddus
1Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Summary
Mitogen-inducible gene 6 (Mig-6) is crucial for normal development and acts as a tumor suppressor. Researchers created a Mig-6 conditional knockout mouse model to study its specific functions in different tissues.
Area of Science:
- Molecular Biology
- Genetics
- Developmental Biology
Background:
- Mitogen-inducible gene 6 (Mig-6) is a stress-induced gene.
- Mig-6 negatively regulates epidermal growth factor (EGF) signaling.
- Mig-6 functions as a tumor suppressor, and its absence causes embryo lethality and tissue abnormalities.
Purpose of the Study:
- To understand the physiological roles of Mig-6.
- To generate and validate a conditional null allele of Mig-6 for tissue-specific functional studies.
Main Methods:
- Generation of a conditional null allele, Mig-6(f/f), by flanking exons 2 and 4 with LoxP sites.
- Creation of recombined Mig-6(-/-) mice using the Zp3-Cre system.
- Confirmation of the conditional null allele via gene expression analysis in various tissues (liver, lung, uterus, skin).
Main Results:
- The Mig-6(f/f) allele was successfully validated.
- Recombined Mig-6(-/-) mice exhibited pathological changes including degenerative joint disease, skin hyperplasia, and uterine abnormalities (enlarged uteri with endometrial hyperplasia).
- These phenotypes resemble those of previously reported Mig-6 germline null alleles.
Conclusions:
- The generated Mig-6(f/f) mouse model is a valuable tool for investigating Mig-6 gene function.
- This model allows for tissue-specific functional studies of Mig-6.
- The findings highlight the critical role of Mig-6 in preventing specific pathological conditions.
Related Concept Videos
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.
Mutation, Gene Flow, and Genetic Drift
In a population that is not at Hardy-Weinberg equilibrium, the frequency of alleles changes over time. Therefore, any deviations from the five conditions of Hardy-Weinberg equilibrium can alter the genetic variation of a given population. Conditions that change the genetic variability of a population include mutations, natural selection, non-random mating, gene flow, and genetic drift (small population size).Mechanisms of Genetic VariationThe original sources of genetic variation are mutations,...
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...
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...
Point and Frameshift Mutations
Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...
Lethal Alleles
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...

