Literature DB >> 10950307

DNA repeat expansions and human disease.

K Usdin1, E Grabczyk.   

Abstract

The repeat expansion diseases are genetic disorders caused by intergenerational expansions of a specific tandem DNA repeat. These disorders range from mildly to severely debilitating or fatal, and all have limited treatment options. How expansion occurs and causes disease is only now beginning to be understood. Efforts to model expansion in mice have so far met with only limited success, perhaps due to a requirement for specific cis- or trans-acting factors. In vitro studies and data from bacteria and yeast suggest that in addition to secondary structures formed by the repeats, components of the DNA replication and recombination machinery are important determinants of instability. The consequences of expansion differ depending on where in the gene the repeat tract is located, and range from reduction of transcription initiation to protein toxicity. Recent advances are beginning to make rational approaches to the development of therapies possible.

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Year:  2000        PMID: 10950307     DOI: 10.1007/PL00000734

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  36 in total

1.  Replication stalling at Friedreich's ataxia (GAA)n repeats in vivo.

Authors:  Maria M Krasilnikova; Sergei M Mirkin
Journal:  Mol Cell Biol       Date:  2004-03       Impact factor: 4.272

2.  Somatic mosaicism in Wiskott--Aldrich syndrome suggests in vivo reversion by a DNA slippage mechanism.

Authors:  T Wada; S H Schurman; M Otsu; E K Garabedian; H D Ochs; D L Nelson; F Candotti
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

Review 3.  Genome analyses substantiate male mutation bias in many species.

Authors:  Melissa A Wilson Sayres; Kateryna D Makova
Journal:  Bioessays       Date:  2011-10-18       Impact factor: 4.345

Review 4.  Replication fork stalling at natural impediments.

Authors:  Ekaterina V Mirkin; Sergei M Mirkin
Journal:  Microbiol Mol Biol Rev       Date:  2007-03       Impact factor: 11.056

5.  Diverse effects of individual mismatch repair components on transcription-induced CAG repeat instability in human cells.

Authors:  Yunfu Lin; John H Wilson
Journal:  DNA Repair (Amst)       Date:  2009-06-03

6.  Lambda exonuclease digestion of CGG trinucleotide repeats.

Authors:  R S Conroy; A P Koretsky; J Moreland
Journal:  Eur Biophys J       Date:  2009-06-27       Impact factor: 1.733

7.  CpG dinucleotides and the mutation rate of non-CpG DNA.

Authors:  Jean-Claude Walser; Loïc Ponger; Anthony V Furano
Journal:  Genome Res       Date:  2008-06-11       Impact factor: 9.043

8.  Counting CAG repeats in the Huntington's disease gene by restriction endonuclease EcoP15I cleavage.

Authors:  Elisabeth Möncke-Buchner; Stefanie Reich; Merlind Mücke; Monika Reuter; Walter Messer; Erich E Wanker; Detlev H Krüger
Journal:  Nucleic Acids Res       Date:  2002-08-15       Impact factor: 16.971

9.  Coordinated processing of 3' slipped (CAG)n/(CTG)n hairpins by DNA polymerases β and δ preferentially induces repeat expansions.

Authors:  Nelson L S Chan; Jinzhen Guo; Tianyi Zhang; Guogen Mao; Caixia Hou; Fenghua Yuan; Jian Huang; Yanbin Zhang; Jianxin Wu; Liya Gu; Guo-Min Li
Journal:  J Biol Chem       Date:  2013-04-12       Impact factor: 5.157

10.  ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice.

Authors:  Ali Entezam; Karen Usdin
Journal:  Nucleic Acids Res       Date:  2009-08-26       Impact factor: 16.971

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