» Articles » PMID: 21080277

Inducible Transgenic Mouse Models

Overview
Specialty Molecular Biology
Date 2010 Nov 17
PMID 21080277
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Inducible transgenic mouse models allow for the activation of genes in specific cells and tissues at specific times. Expression levels are dependent on the dose of the agent administered. Effective experimental models are characterized by low background levels of the regulated gene and induction to high levels with sub-physiological levels of inducing agents. The most commonly used methods to control gene expression in mouse models are based on the tet-operon/repressor bi-transgenic system and the estrogen receptor (ER) ligand-binding domain. Less commonly used systems to control gene expression in transgenic mice take advantage of the ligand-binding domain of the progesterone receptor, and the lac and GAL4 inducible systems. The tetracycline-regulated transgenic models are typically designed to activate the expression of the gene of interest in a specific cell type at a specific point in time. The ER is most commonly fused with Cre recombinase, although it can be used with transcription factors, kinases, etc., that are active in the nucleus. Cre-ER transgenes allow for the induction of recombinase activity in specific cells at defined time points. Cre recombinase is most often found in combination with conditional alleles to inactivate gene expression. When used for gene activation, Cre removes stop cassettes from transgenes and thus allows the expression of reporter or other molecules. Thus, the tetracycline-regulated and Cre-ER systems are complementary in mouse models, with utility in the cell-specific activation and inactivation of gene expression.

Citing Articles

Assessment of Antimicrobial Therapy in Eradicating Chlamydia muridarum in Research Mice: Immune Status and Its Impact on Outcomes.

Palillo M, Carrasco S, Mishkin N, Palillo J, Lynch D, Lawton S J Am Assoc Lab Anim Sci. 2025; 64(1):76-88.

PMID: 40035285 PMC: 11808367. DOI: 10.30802/AALAS-JAALAS-24-069.


Genomic predictors of radiation response: recent progress towards personalized radiotherapy for brain metastases.

Harary P, Rajaram S, Chen M, Hori Y, Park D, Chang S Cell Death Discov. 2024; 10(1):501.

PMID: 39695143 PMC: 11655559. DOI: 10.1038/s41420-024-02270-2.


RuX: A Novel, Flexible, and Sensitive Mifepristone-Induced Transcriptional Regulation System.

Meinzinger A, Zsigmond A, Horvath P, Kellenberger A, Parej K, Tallone T Int J Cell Biol. 2023; 2023:7121512.

PMID: 37941807 PMC: 10630016. DOI: 10.1155/2023/7121512.


Skeletal muscle Nox4 knockout prevents and Nox2 knockout blunts loss of maximal diaphragm force in mice with heart failure with reduced ejection fraction.

Kumar R, Hahn D, Kelley R, Muscato D, Shamoun A, Curbelo-Bermudez N Free Radic Biol Med. 2022; 194:23-32.

PMID: 36436728 PMC: 10191720. DOI: 10.1016/j.freeradbiomed.2022.11.025.


The inclusion membrane protein IncS is critical for initiation of the Chlamydia intracellular developmental cycle.

Cortina M, Bishop R, DeVasure B, Coppens I, Derre I PLoS Pathog. 2022; 18(9):e1010818.

PMID: 36084160 PMC: 9491573. DOI: 10.1371/journal.ppat.1010818.