Literature DB >> 18166978

Features of trinucleotide repeat instability in vivo.

Irina V Kovtun1, Cynthia T McMurray.   

Abstract

Unstable repeats are associated with various types of cancer and have been implicated in more than 40 neurodegenerative disorders. Trinucleotide repeats are located in non-coding and coding regions of the genome. Studies of bacteria, yeast, mice and man have helped to unravel some features of the mechanism of trinucleotide expansion. Looped DNA structures comprising trinucleotide repeats are processed during replication and/or repair to generate deletions or expansions. Most in vivo data are consistent with a model in which expansion and deletion occur by different mechanisms. In mammals, microsatellite instability is complex and appears to be influenced by genetic, epigenetic and developmental factors.

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Year:  2008        PMID: 18166978     DOI: 10.1038/cr.2008.5

Source DB:  PubMed          Journal:  Cell Res        ISSN: 1001-0602            Impact factor:   25.617


  77 in total

1.  In vitro repair of DNA hairpins containing various numbers of CAG/CTG trinucleotide repeats.

Authors:  Tianyi Zhang; Jian Huang; Liya Gu; Guo-Min Li
Journal:  DNA Repair (Amst)       Date:  2011-10-29

2.  Chromosomal detection of simple sequence repeats (SSRs) using nondenaturing FISH (ND-FISH).

Authors:  Ángeles Cuadrado; Nicolás Jouve
Journal:  Chromosoma       Date:  2010-10       Impact factor: 4.316

3.  Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats.

Authors:  Masayuki Nakamori; Christopher E Pearson; Charles A Thornton
Journal:  Hum Mol Genet       Date:  2010-11-18       Impact factor: 6.150

4.  Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders.

Authors:  Xiao-Nan Zhao; Daman Kumari; Shikha Gupta; Di Wu; Maya Evanitsky; Wei Yang; Karen Usdin
Journal:  Hum Mol Genet       Date:  2015-09-29       Impact factor: 6.150

5.  Inhibition of Aggregation of Mutant Huntingtin by Nucleic Acid Aptamers In Vitro and in a Yeast Model of Huntington's Disease.

Authors:  Rajeev K Chaudhary; Kinjal A Patel; Milan K Patel; Radha H Joshi; Ipsita Roy
Journal:  Mol Ther       Date:  2015-08-27       Impact factor: 11.454

6.  Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1.

Authors:  Sonal Datta; Mohammad Parwez Alam; Subeer S Majumdar; Abhishek Kumar Mehta; Souvik Maiti; Neerja Wadhwa; Vani Brahmachari
Journal:  Chromosome Res       Date:  2011-04-16       Impact factor: 5.239

7.  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

Review 8.  Mutation spectra in fragile X syndrome induced by deletions of CGG*CCG repeats.

Authors:  Robert D Wells
Journal:  J Biol Chem       Date:  2008-10-28       Impact factor: 5.157

9.  Double-strand break repair pathways protect against CAG/CTG repeat expansions, contractions and repeat-mediated chromosomal fragility in Saccharomyces cerevisiae.

Authors:  Rangapriya Sundararajan; Lionel Gellon; Rachel M Zunder; Catherine H Freudenreich
Journal:  Genetics       Date:  2009-11-09       Impact factor: 4.562

10.  The Rtt109 histone acetyltransferase facilitates error-free replication to prevent CAG/CTG repeat contractions.

Authors:  Jiahui H Yang; Catherine H Freudenreich
Journal:  DNA Repair (Amst)       Date:  2010-01-18
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