Inner Ear-Specific Cre Mouse Model for Targeted Gene Deletion and Hearing Loss Research

Case ID:
C15757

JHU Ref #: C15757

Value Proposition

·        Inner ear specificity: When bred with a mouse with a floxed gene of interest (GOI), the offspring will not express the GOI in the inner ear.

·        Applicable in multiple hearing models: Researchers can study effects of a GOI in the inner ear in both deaf and hearing mice.

·        Improved mouse line stability: The novel knock-in Cre model is more stable than other transgenic mice.

·        Broad compatibility: The mouse can be bred with any floxed GOI mouse to create novel research animals.

·        Non-lethal crosses: Researchers can simultaneously study the removal of a GOI and Tecta in the inner ear without the mortality observed in a simple GOI deletion.

Unmet Need

·        There are very few mouse lines for specifically manipulating gene expression in the inner ear.

·        Many mouse lines used in such research are not specific to the inner ear and modulate gene expression throughout the entire body.

·        Other simple transgenic Cre mice may have low stability or unpredictable side effects. These mouse lines may not be viable or accurate models for deafness research.

·        Therefore, there is a strong need to develop a mouse model that can selectively manipulate gene expression within the inner ear.

Technology Description

·        Novel transgenic mouse line with an insertion of the Cre gene in place of the Tecta gene.

·        Insertion of Cre eliminates Tecta expression, causing hearing loss.

·        The mouse line can be bred with floxed transgenic mice to specifically silence a GOI in the inner ear. Heterozygous Tecta-Cre mice retain Tecta expression and normal hearing.

Stage of Development

·        The mouse cell line is completed and is cryopreserved.

·        It is available on JAX as stock #035552.

Data Availability

·        Data available upon request.

Publication

·        Babola, T. A., Kersbergen, C. J., Wang, C. H., Bergles, D. E. (2020). Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space. eLife, 9, e52160. https://doi.org/10.7554/eLife.52160

Patent Information:
Inventors:
Category(s):
Get custom alerts for techs in these categories/from these inventors:
For Information, Contact:
Licensing Biomaterials
JHTVBioMaterials@jhu.edu
410-614-0300
Save This Technology:
2017 - 2022 © Johns Hopkins Technology Ventures. All Rights Reserved. Powered by Inteum