Literature DB >> 26649459

Forward Genetic Approach to Uncover Stress Resistance Genes in Mice - A High-throughput Screen in ES Cells.

Michael Ludwig1, David Kitzenberg1, Wallace S Chick2.   

Abstract

Phenotype-driven genetic screens in mice is a powerful technique to uncover gene functions, but are often hampered by extremely high costs, which severely limits its potential. We describe here the use of mouse embryonic stem (ES) cells as surrogate cells to screen for a phenotype of interest and subsequently introduce these cells into a host embryo to develop into a living mouse carrying the phenotype. This method provides (1) a cost effective, high-throughput platform for genetic screen in mammalian cells; (2) a rapid way to identify the mutated genes and verify causality; and (3) a short-cut to develop mouse mutants directly from these selected ES cells for whole animal studies. We demonstrated the use of paraquat (PQ) to select resistant mutants and identify mutations that confer oxidative stress resistance. Other stressors or cytotoxic compounds may also be used to screen for resistant mutants to uncover novel genetic determinants of a variety of cellular stress resistance.

Entities:  

Year:  2015        PMID: 26649459      PMCID: PMC4692703          DOI: 10.3791/53062

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  14 in total

1.  Multiplex stress resistance in cells from long-lived dwarf mice.

Authors:  Shin Murakami; Adam Salmon; Richard A Miller
Journal:  FASEB J       Date:  2003-06-03       Impact factor: 5.191

Review 2.  Nonsense-mediated mRNA decay: terminating erroneous gene expression.

Authors:  Kristian E Baker; Roy Parker
Journal:  Curr Opin Cell Biol       Date:  2004-06       Impact factor: 8.382

3.  Genomic DNA microextraction: a method to screen numerous samples.

Authors:  R Ramírez-Solis; J Rivera-Pérez; J D Wallace; M Wims; H Zheng; A Bradley
Journal:  Anal Biochem       Date:  1992-03       Impact factor: 3.365

4.  A piggyBac transposon-based genome-wide library of insertionally mutated Blm-deficient murine ES cells.

Authors:  Wei Wang; Allan Bradley; Yue Huang
Journal:  Genome Res       Date:  2009-02-20       Impact factor: 9.043

5.  Functional annotation of mouse mutations in embryonic stem cells by use of expression profiling.

Authors:  Derek J Symula; Yiwen Zhu; John C Schimenti; Edward M Rubin
Journal:  Mamm Genome       Date:  2004-01       Impact factor: 2.957

6.  Transmission of mutant phenotypes from ES cells to adult mice.

Authors:  Wallace S Chick; Derek A Drechsel; Warren Hammond; Manisha Patel; Thomas E Johnson
Journal:  Mamm Genome       Date:  2009-10-01       Impact factor: 2.957

7.  A public gene trap resource for mouse functional genomics.

Authors:  William C Skarnes; Harald von Melchner; Wolfgang Wurst; Geoff Hicks; Alex S Nord; Tony Cox; Stephen G Young; Patricia Ruiz; Phil Soriano; Marc Tessier-Lavigne; Bruce R Conklin; William L Stanford; Janet Rossant
Journal:  Nat Genet       Date:  2004-06       Impact factor: 38.330

8.  Suppression of nonsense-mediated mRNA decay permits unbiased gene trapping in mouse embryonic stem cells.

Authors:  Toshiaki Shigeoka; Masashi Kawaichi; Yasumasa Ishida
Journal:  Nucleic Acids Res       Date:  2005-02-01       Impact factor: 16.971

9.  Screening for stress-resistance mutations in the mouse.

Authors:  Wallace S Chick; Michael Ludwig; Xiaoyun Zhao; David Kitzenberg; Kristina Williams; Thomas E Johnson
Journal:  Front Genet       Date:  2014-09-08       Impact factor: 4.599

10.  The overexpression of major antioxidant enzymes does not extend the lifespan of mice.

Authors:  Viviana I Pérez; Holly Van Remmen; Alex Bokov; Charles J Epstein; Jan Vijg; Arlan Richardson
Journal:  Aging Cell       Date:  2008-12-11       Impact factor: 9.304

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