A collection of genetic mouse lines and related tools for inducible and reversible intersectional misexpression

Author:

Ahmadzadeh Elham1,Bayin N. Sumru2,Qu Xinli1,Singh Aditi1,Madisen Linda3,Stephen Daniel2,Zeng Hongkui3,Joyner Alexandra L.2,Rosello-Diez Alberto1ORCID

Affiliation:

1. Australian Regenerative Medicine Institute, Monash University. Clayton, VIC 3800. Australia

2. Developmental Biology Program. Sloan Kettering Institute. New York, NY 10065. USA

3. Allen Institute for Brain Science. Seattle, WA 98109. USA

Abstract

Thanks to many advances in genetic manipulation, mouse models have become very powerful in their ability to interrogate biological processes. In order to precisely target expression of a gene of interest to particular cell types, intersectional genetic approaches utilizing two promoter/enhancers unique to a cell type are ideal. Within these methodologies, variants that add temporal control of gene expression are the most powerful. We describe the development, validation and application of an intersectional approach that involves three transgenes, requiring the intersection of two promoter/enhancers to target gene expression to precise cell types. Furthermore, the approach utilizes available lines expressing tTA/rTA to control timing of gene expression based on whether doxycycline is absent or present, respectively. We also show that the approach can be extended to other animal models, using chicken embryos. We generated three mouse lines targeted at the Tigre (Igs7) locus with TRE-loxP-tdTomato-loxP upstream of three genes (p21, DTA and Ctgf) and combined them with Cre and tTA/rtTA lines that target expression to the cerebellum and limbs. Our tools will facilitate unraveling biological questions in multiple fields and organisms.

Funder

Human Frontier Science Program

Charles H. Revson Foundation

National Institutes of Health

New York Stem Cell Foundation

Islamic Development Bank

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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