Literature DB >> 17331550

The effects of MSH2 deficiency on spontaneous and radiation-induced mutation rates in the mouse germline.

Karen L-A Burr1, Annemarie van Duyn-Goedhart, Peter Hickenbotham, Karen Monger, Paul P W van Buul, Yuri E Dubrova.   

Abstract

Mutation rates at two expanded simple tandem repeat (ESTR) loci were studied in the germline of mismatch repair deficient Msh2 knock-out mice. Spontaneous mutation rates in homozygous Msh2(-/-) males were significantly higher than those in isogenic wild-type (Msh2(+/+)) and heterozygous (Msh2(+/-)) mice. In contrast, the irradiated Msh2(-/-) mice did not show any detectable increases in their mutation rate, whereas significant ESTR mutation induction was observed in the irradiated Msh2(+/+) and Msh2(+/-) animals. Considering these data and the results of other publications, we propose that the Msh2-deficient mice possess a mutator phenotype in their germline and somatic tissues while the loss of a single Msh2 allele does not affect the stability of heterozygotes.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17331550     DOI: 10.1016/j.mrfmmm.2007.01.010

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  8 in total

1.  The cellular, developmental and population-genetic determinants of mutation-rate evolution.

Authors:  Michael Lynch
Journal:  Genetics       Date:  2008-08-30       Impact factor: 4.562

2.  A novel mouse model of cerebral cavernous malformations based on the two-hit mutation hypothesis recapitulates the human disease.

Authors:  David A McDonald; Robert Shenkar; Changbin Shi; Rebecca A Stockton; Amy L Akers; Melanie H Kucherlapati; Raju Kucherlapati; James Brainer; Mark H Ginsberg; Issam A Awad; Douglas A Marchuk
Journal:  Hum Mol Genet       Date:  2010-10-11       Impact factor: 6.150

3.  Progression inference for somatic mutations in cancer.

Authors:  Leif E Peterson; Tatiana Kovyrshina
Journal:  Heliyon       Date:  2017-04-11

4.  Loss of Msh2 and a single-radiation hit induce common, genome-wide, and persistent epigenetic changes in the intestine.

Authors:  Maria Herberg; Susann Siebert; Marianne Quaas; Torsten Thalheim; Karen Rother; Michelle Hussong; Janine Altmüller; Christiane Kerner; Joerg Galle; Michal R Schweiger; Gabriela Aust
Journal:  Clin Epigenetics       Date:  2019-04-27       Impact factor: 6.551

5.  Somatic maintenance impacts the evolution of mutation rate.

Authors:  Andrii Rozhok; James DeGregori
Journal:  BMC Evol Biol       Date:  2019-08-23       Impact factor: 3.260

Review 6.  Mutation Induction in Humans and Mice: Where Are We Now?

Authors:  Yuri Dubrova
Journal:  Cancers (Basel)       Date:  2019-11-01       Impact factor: 6.639

Review 7.  Lynch Syndrome: From Carcinogenesis to Prevention Interventions.

Authors:  Donatella Gambini; Stefano Ferrero; Elisabetta Kuhn
Journal:  Cancers (Basel)       Date:  2022-08-24       Impact factor: 6.575

8.  MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.

Authors:  Stéphanie Tomé; Kevin Manley; Jodie P Simard; Greg W Clark; Meghan M Slean; Meera Swami; Peggy F Shelbourne; Elisabeth R M Tillier; Darren G Monckton; Anne Messer; Christopher E Pearson
Journal:  PLoS Genet       Date:  2013-02-28       Impact factor: 5.917

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.