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A Most Formidable Arsenal: Genetic Technologies for Building a Better Mouse

Overview
Journal Genes Dev
Specialty Molecular Biology
Date 2020 Oct 2
PMID 33004485
Citations 21
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Abstract

The mouse is one of the most widely used model organisms for genetic study. The tools available to alter the mouse genome have developed over the preceding decades from forward screens to gene targeting in stem cells to the recent influx of CRISPR approaches. In this review, we first consider the history of mice in genetic study, the development of classic approaches to genome modification, and how such approaches have been used and improved in recent years. We then turn to the recent surge of nuclease-mediated techniques and how they are changing the field of mouse genetics. Finally, we survey common classes of alleles used in mice and discuss how they might be engineered using different methods.

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References
1.
Heigwer F, Kerr G, Boutros M . E-CRISP: fast CRISPR target site identification. Nat Methods. 2014; 11(2):122-3. DOI: 10.1038/nmeth.2812. View

2.
Lee C, Barber G, Casper J, Clawson H, Diekhans M, Gonzalez J . UCSC Genome Browser enters 20th year. Nucleic Acids Res. 2019; 48(D1):D756-D761. PMC: 7145642. DOI: 10.1093/nar/gkz1012. View

3.
Wang Y, Schnegelsberg P, Dausman J, Jaenisch R . Functional redundancy of the muscle-specific transcription factors Myf5 and myogenin. Nature. 1996; 379(6568):823-5. DOI: 10.1038/379823a0. View

4.
Wang W, Kutny P, Byers S, Longstaff C, DaCosta M, Pang C . Delivery of Cas9 Protein into Mouse Zygotes through a Series of Electroporation Dramatically Increases the Efficiency of Model Creation. J Genet Genomics. 2016; 43(5):319-27. PMC: 4892940. DOI: 10.1016/j.jgg.2016.02.004. View

5.
Poulin J, Pereira Luppi M, Hofer C, Caronia G, Hsu P, Chan C . PRISM: A Progenitor-Restricted Intersectional Fate Mapping Approach Redefines Forebrain Lineages. Dev Cell. 2020; 53(6):740-753.e3. PMC: 7778471. DOI: 10.1016/j.devcel.2020.05.019. View