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Generation of Genetically Modified Mice through the Microinjection of Oocytes
Published on: June 15, 2017
Novel approaches to in vitro transgenesis
A D Adamson1, D Jackson, J R E Davis
1Faculty of Life Sciences, Manchester Interdisciplinary Biocentre, University of Manchester, Manchester, UK. antony.adamson@manchester.ac.uk
The Journal of Endocrinology
|December 8, 2010
Summary
This review explores methods for studying eukaryote gene expression in vitro. It details various transgenesis systems and expression vectors, highlighting popular choices like bacterial artificial chromosomes and episomal vectors for accurate gene expression analysis.
Area of Science:
- Molecular Biology
- Genetics
Background:
- Gene expression is crucial for understanding biological processes.
- Diverse methods exist to study gene expression, from in vitro assays to whole organisms.
- Choosing the right model system is vital for experimental design.
Purpose of the Study:
- To review in vitro techniques for studying eukaryote gene expression.
- To compare advantages and disadvantages of various transgenesis systems.
- To highlight emerging and popular expression systems.
Main Methods:
- Review of existing literature on gene expression techniques.
- Analysis of transgene integration mechanisms (transient vs. stable).
- Comparison of transgenesis systems: plasmids, viruses, targeted integration, knock-in approaches.
Main Results:
- Discussion of bacterial artificial chromosomes and episomal vectors as advantageous expression systems.
- Identification of novel approaches combining techniques for complex, accurate expression systems.
- Evaluation of pros and cons for each described method.
Conclusions:
- Selection of appropriate in vitro gene expression systems is critical for research.
- Bacterial artificial chromosomes and episomal vectors offer significant advantages.
- Novel combined approaches enhance physiological accuracy in gene expression studies.
Related Concept Videos
Transgenic Organisms
Overview
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.
Transgenic Plants
Recombinant DNA technology called transgenesis is often used to add a foreign gene or remove a detrimental gene from an organism. Such genetically modified organisms are called transgenic organisms.
The first-ever transgenic plant was a tobacco plant developed in 1983 that showed resistance against the tobacco mosaic virus. Since then, many transgenic plants have been developed and commercialized for improving the agricultural, ornamental, and horticultural value of a crop plant. Transgenic...
The first-ever transgenic plant was a tobacco plant developed in 1983 that showed resistance against the tobacco mosaic virus. Since then, many transgenic plants have been developed and commercialized for improving the agricultural, ornamental, and horticultural value of a crop plant. Transgenic...
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.

