Literature DB >> 33925919

The Startling Role of Mismatch Repair in Trinucleotide Repeat Expansions.

Guy-Franck Richard1.   

Abstract

Trinucleotide repeats are a peculiar class of microsatellites whose expansions are responsible for approximately 30 human neurological or developmental disorders. The molecular mechanisms responsible for these expansions in humans are not totally understood, but experiments in model systems such as yeast, transgenic mice, and human cells have brought evidence that the mismatch repair machinery is involved in generating these expansions. The present review summarizes, in the first part, the role of mismatch repair in detecting and fixing the DNA strand slippage occurring during microsatellite replication. In the second part, key molecular differences between normal microsatellites and those that show a bias toward expansions are extensively presented. The effect of mismatch repair mutants on microsatellite expansions is detailed in model systems, and in vitro experiments on mismatched DNA substrates are described. Finally, a model presenting the possible roles of the mismatch repair machinery in microsatellite expansions is proposed.

Entities:  

Keywords:  MutL; MutS; microsatellites; mismatch repair; trinucleotide repeats

Year:  2021        PMID: 33925919     DOI: 10.3390/cells10051019

Source DB:  PubMed          Journal:  Cells        ISSN: 2073-4409            Impact factor:   6.600


  96 in total

1.  The mismatch repair system protects against intergenerational GAA repeat instability in a Friedreich ataxia mouse model.

Authors:  Vahid Ezzatizadeh; Ricardo Mouro Pinto; Chiranjeevi Sandi; Madhavi Sandi; Sahar Al-Mahdawi; Hein Te Riele; Mark A Pook
Journal:  Neurobiol Dis       Date:  2012-01-20       Impact factor: 5.996

2.  Trinucleotide repeats that expand in human disease form hairpin structures in vitro.

Authors:  A M Gacy; G Goellner; N Juranić; S Macura; C T McMurray
Journal:  Cell       Date:  1995-05-19       Impact factor: 41.582

Review 3.  Mini- and microsatellite expansions: the recombination connection.

Authors:  G F Richard; F Pâques
Journal:  EMBO Rep       Date:  2000-08       Impact factor: 8.807

4.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors:  A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal:  Cell       Date:  1991-05-31       Impact factor: 41.582

5.  A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders.

Authors:  Bruce E Hayward; Peter J Steinbach; Karen Usdin
Journal:  Nucleic Acids Res       Date:  2020-07-03       Impact factor: 16.971

6.  Large-scale expansions of Friedreich's ataxia GAA repeats in yeast.

Authors:  Alexander A Shishkin; Irina Voineagu; Robert Matera; Nicole Cherng; Brook T Chernet; Maria M Krasilnikova; Vidhya Narayanan; Kirill S Lobachev; Sergei M Mirkin
Journal:  Mol Cell       Date:  2009-07-10       Impact factor: 17.970

7.  Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli.

Authors:  S Kang; A Jaworski; K Ohshima; R D Wells
Journal:  Nat Genet       Date:  1995-06       Impact factor: 38.330

8.  Extrahelical (CAG)/(CTG) triplet repeat elements support proliferating cell nuclear antigen loading and MutLα endonuclease activation.

Authors:  Anna Pluciennik; Vickers Burdett; Celia Baitinger; Ravi R Iyer; Kevin Shi; Paul Modrich
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-09       Impact factor: 11.205

9.  Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.

Authors:  Ricardo Mouro Pinto; Ella Dragileva; Andrew Kirby; Alejandro Lloret; Edith Lopez; Jason St Claire; Gagan B Panigrahi; Caixia Hou; Kim Holloway; Tammy Gillis; Jolene R Guide; Paula E Cohen; Guo-Min Li; Christopher E Pearson; Mark J Daly; Vanessa C Wheeler
Journal:  PLoS Genet       Date:  2013-10-31       Impact factor: 5.917

10.  MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.

Authors:  Michael Flower; Vilija Lomeikaite; Marc Ciosi; Sarah Cumming; Fernando Morales; Kitty Lo; Davina Hensman Moss; Lesley Jones; Peter Holmans; Darren G Monckton; Sarah J Tabrizi
Journal:  Brain       Date:  2019-06-19       Impact factor: 13.501

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  2 in total

Review 1.  Myotonic Dystrophies: A Genetic Overview.

Authors:  Payam Soltanzadeh
Journal:  Genes (Basel)       Date:  2022-02-17       Impact factor: 4.096

2.  Prognostic and immunological role of Ras-related protein Rap1b in pan-cancer.

Authors:  Guoliang Cui; Can Wang; Zhenyan Lin; Xiaoke Feng; Muxin Wei; Zhengyue Miao; Zhiguang Sun; Fei Wei
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

  2 in total

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