Literature DB >> 23598974

Defining a genotoxic profile with mouse embryonic stem cells.

Tae Moon Kim1, Vivienne I Rebel, Paul Hasty.   

Abstract

Many genotoxins are found in the environment from synthetic to natural, yet very few have been studied in depth. This means we fail to understand many molecules that damage DNA, we do not understand the type of damage they cause and the repair pathways required to correct their lesions. It is surprising so little is known about the vast majority of genotoxins since they have potential to cause disease from developmental defects to cancer to degenerative ailments. By contrast, some of these molecules have commercial and medical potential and some can be weaponized. Therefore, we need a systematic method to efficiently generate a genotoxic profile for these agents. A genotoxic profile would include the type of damage the genotoxin causes, the pathways used to repair the damage and the resultant mutations if repair fails. Mouse embryonic stem (ES) cells are well suited for identifying pathways and mutations. Mouse ES cells are genetically tractable and many DNA repair mutant cells are available. ES cells have a high mitotic index and form colonies so experiments can be completed quickly and easily. Furthermore, ES cells have robust DNA repair pathways to minimize genetic mutations at a particularly vulnerable time in life, early development when a mutation in a single cell could ultimately contribute to a large fraction of the individual. After an initial screen, other types of cells and mouse models can be used to complement the analysis. This review discusses the merging field of genotoxic screens in mouse ES cells that can be used to discover and study potential genotoxic activity for chemicals commonly found in our environment.

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Year:  2013        PMID: 23598974      PMCID: PMC4075448          DOI: 10.1177/1535370213480700

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


  103 in total

1.  The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells.

Authors:  L J Niedernhofer; J Essers; G Weeda; B Beverloo; J de Wit; M Muijtjens; H Odijk; J H Hoeijmakers; R Kanaar
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

Review 2.  Repair and genetic consequences of endogenous DNA base damage in mammalian cells.

Authors:  Deborah E Barnes; Tomas Lindahl
Journal:  Annu Rev Genet       Date:  2004       Impact factor: 16.830

3.  Inhibition of topoisomerase II by antitumor agents bis(2,6-dioxopiperazine) derivatives.

Authors:  K Tanabe; Y Ikegami; R Ishida; T Andoh
Journal:  Cancer Res       Date:  1991-09-15       Impact factor: 12.701

4.  Ionizing radiation is a potent inducer of mitotic recombination in mouse embryonic stem cells.

Authors:  Natalia G Denissova; Irina V Tereshchenko; Eric Cui; Peter J Stambrook; Changshun Shao; Jay A Tischfield
Journal:  Mutat Res       Date:  2011-07-23       Impact factor: 2.433

Review 5.  Relative susceptibilities of male germ cells to genetic defects induced by cancer chemotherapies.

Authors:  Andrew J Wyrobek; Thomas E Schmid; Francesco Marchetti
Journal:  J Natl Cancer Inst Monogr       Date:  2005

6.  Hydroxyurea-stalled replication forks become progressively inactivated and require two different RAD51-mediated pathways for restart and repair.

Authors:  Eva Petermann; Manuel Luís Orta; Natalia Issaeva; Niklas Schultz; Thomas Helleday
Journal:  Mol Cell       Date:  2010-02-26       Impact factor: 17.970

7.  A genotoxic screen: rapid analysis of cellular dose-response to a wide range of agents that either damage DNA or alter genome maintenance pathways.

Authors:  Teresa Marple; Han Li; Paul Hasty
Journal:  Mutat Res       Date:  2004-10-04       Impact factor: 2.433

8.  Cytoskeletal control of fibroblast length: experiments with linear strips of substrate.

Authors:  E M Levina; M A Kharitonova; Y A Rovensky; J M Vasiliev
Journal:  J Cell Sci       Date:  2001-12       Impact factor: 5.285

9.  Limiting the persistence of a chromosome break diminishes its mutagenic potential.

Authors:  Nicole Bennardo; Amanda Gunn; Anita Cheng; Paul Hasty; Jeremy M Stark
Journal:  PLoS Genet       Date:  2009-10-16       Impact factor: 5.917

10.  Phosphorylation of histone H2B at DNA double-strand breaks.

Authors:  Oscar Fernandez-Capetillo; C David Allis; André Nussenzweig
Journal:  J Exp Med       Date:  2004-06-14       Impact factor: 14.307

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  1 in total

1.  A mechanism for 1,4-Benzoquinone-induced genotoxicity.

Authors:  Mi Young Son; Chu-Xia Deng; Jan H Hoeijmarkers; Vivienne I Rebel; Paul Hasty
Journal:  Oncotarget       Date:  2016-07-19
  1 in total

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