4.3 Review

Conditional Gene Expression in the Mouse Inner Ear Using Cre-IoxP

Publisher

SPRINGER
DOI: 10.1007/s10162-012-0324-5

Keywords

cochlea; conditional gene deletion CreER; Cre efficiency; Cre recombinase; ectopic gene expression; Flp recombinase; knock-in; LoxP; reporter lines; Tet-on; Tet-off; transgenic; utricle; vestibular

Funding

  1. National Institute of Health [DC006471, DC008800, DC010310, CA21765]
  2. Office of Naval Research [N000140911014]
  3. Sir Henry Wellcome Trust
  4. American Lebanese Syrian Associated Charities (ALSAC) of St. Jude Children's Research Hospital
  5. The Hartwell Individual Biomedical Research Award

Ask authors/readers for more resources

In recent years, there has been significant progress in the use of Cre- technology for conditional gene expression in the inner ear. Here, we introduce the basic concepts of this powerful technology, emphasizing the differences between Cre and CreER. We describe the creation and Cre expression pattern of each Cre and CreER mouse line that has been reported to have expression in auditory and vestibular organs. We compare the Cre expression patterns between Atoh1-CreER(TM) and Atoh1-CreER(T2) and report a new line, Fgfr3-iCreER(T2), which displays inducible Cre activity in cochlear supporting cells. We also explain how results can vary when transgenic vs. knock-in Cre/CreER alleles are used to alter gene expression. We discuss practical issues that arise when using the Cre- system, such as the use of proper controls, Cre efficiency, reporter expression efficiency, and Cre leakiness. Finally, we introduce other methods for conditional gene expression, including Flp recombinase and the tetracycline-inducible system, which can be combined with Cre- mouse models to investigate conditional expression of more than one gene.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available