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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.
Mouse Models of Cancer Study02:43

Mouse Models of Cancer Study

Mice have long served as models for studying human biology and pathology because of their phylogenetic and physiological similarity with humans. They are also easy to maintain and breed in the laboratory, and hence, many inbred strains are now available for research. Studies on mice have contributed immeasurably to our understanding of cancer biology.
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...

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Related Experiment Video

Updated: Jul 5, 2026

Assessment of Kidney Function in Mouse Models of Glomerular Disease
09:16

Assessment of Kidney Function in Mouse Models of Glomerular Disease

Published on: June 30, 2018

Progress in gene targeting: using mutant mice to study renal function and disease.

Donald E Kohan1

  • 1Division of Nephrology, Department of Internal Medicine, University of Utah Health Sciences Center, Salt Lake City, Utah 84132, USA. donald.kohan@hsc.utah.edu

Kidney International
|April 18, 2008
PubMed
Summary

Genetic engineering in mice advances renal research by enabling precise control over gene expression. New tools offer cell-specific, timed, and reversible gene modification for studying kidney function and disease.

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Area of Science:

  • Nephrology
  • Genetics
  • Molecular Biology

Background:

  • Conventional transgenic approaches have been instrumental in understanding gene function in renal health and disease.
  • Recent advancements allow for controlled cell type, timing, and reversibility of gene expression in mice.
  • Identifying renal cell-specific promoters has improved the interpretation of gene targeting studies.

Purpose of the Study:

  • To review the state-of-the-art in gene targeting techniques in the kidney.
  • To discuss the function, indications, and limitations of molecular biologic tools for renal gene modification.
  • To highlight recent progress and future directions in transgenic mouse models for kidney research.

Main Methods:

  • Utilizing site-specific recombinases (Cre, Flp, PhiC31) for cell-specific gene knockout.
  • Employing doxycycline- and tamoxifen-inducible systems for temporally regulated gene expression.
  • Exploring RNA interference (RNAi) for rapid and reversible gene knockdown.

Main Results:

  • Site-specific recombinases enable precise genetic manipulation in specific kidney cell types.
  • Inducible systems allow for the study of gene function without confounding developmental effects.
  • RNA interference shows potential for gene knockdown, though its utility in renal function studies is still under investigation.

Conclusions:

  • Advanced gene targeting tools significantly enhance the study of renal gene function and disease mechanisms in mice.
  • Cell-specific, temporally controlled, and reversible genetic modifications are crucial for accurate physiological and pathological studies.
  • Ongoing development of new gene targeting technologies promises to further simplify the generation and application of transgenic mouse models for kidney research.