Literature DB >> 11719274

Fragile X syndrome and Friedreich's ataxia: two different paradigms for repeat induced transcript insufficiency.

E Grabczyk1, D Kumari, K Usdin.   

Abstract

DNA repeat expansion is the genetic basis for a growing number of neurological disorders. While the largest subset of these diseases results in an increase in the length of a polyglutamine tract in the protein encoded by the affected gene, the most common form of inherited mental retardation, fragile X syndrome, and the most common inherited ataxia, Friedreich's ataxia, are both caused by expansions that are transcribed but not translated. These expansions both decrease expression of the gene in which the expanded repeat is located, but they do so by quite different mechanisms. In fragile X syndrome, CGG. CCG expansion in the 5' untranslated region of the FMR1 gene leads to hypermethylation of the repeats and the adjacent CpG-rich promoter. Methylation prevents the binding of the transcription factor alpha-Pal/NRF-1, and may indirectly affect the binding of other factors via the formation of transcriptionally silent chromatin. In Friedreich's ataxia, GAA. TTC expansion in an intron of the FRDA gene reduces expression by interfering with transcription elongation. The model that best describes the available data is transcription-driven formation of a transient purine. purine. pyrimidine DNA triplex behind an advancing RNA polymerase. This structure lassoes the RNA polymerase that caused it, trapping the enzyme on the template.

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Year:  2001        PMID: 11719274     DOI: 10.1016/s0361-9230(01)00572-x

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  7 in total

Review 1.  Friedreich ataxia-update on pathogenesis and possible therapies.

Authors:  Max Voncken; Panos Ioannou; Martin B Delatycki
Journal:  Neurogenetics       Date:  2003-12-19       Impact factor: 2.660

Review 2.  Friedreich's Ataxia: from the (GAA)n repeat mediated silencing to new promising molecules for therapy.

Authors:  Daniele Marmolino; Fabio Acquaviva
Journal:  Cerebellum       Date:  2009-01-23       Impact factor: 3.847

3.  Comparative (computational) analysis of the DNA methylation status of trinucleotide repeat expansion diseases.

Authors:  Mohammadmersad Ghorbani; Simon J E Taylor; Mark A Pook; Annette Payne
Journal:  J Nucleic Acids       Date:  2013-12-23

4.  Single nucleotide polymorphisms and microsatellites in the canine glutathione S-transferase pi 1 (GSTP1) gene promoter.

Authors:  James Sacco; Sarah Mann; Keller Toral
Journal:  Canine Genet Epidemiol       Date:  2017-10-11

5.  A deeper view into the significance of simple sequence repeats in pre-miRNAs provides clues for its possible roles in determining the function of microRNAs.

Authors:  Nisha Joy; Y P Maimoonath Beevi; E V Soniya
Journal:  BMC Genet       Date:  2018-05-09       Impact factor: 2.797

6.  A persistent RNA.DNA hybrid formed by transcription of the Friedreich ataxia triplet repeat in live bacteria, and by T7 RNAP in vitro.

Authors:  Ed Grabczyk; Miriam Mancuso; Mimi C Sammarco
Journal:  Nucleic Acids Res       Date:  2007-08-09       Impact factor: 16.971

7.  Computational investigation of RNA CUG repeats responsible for myotonic dystrophy 1.

Authors:  Ilyas Yildirim; Debayan Chakraborty; Matthew D Disney; David J Wales; George C Schatz
Journal:  J Chem Theory Comput       Date:  2015-10-13       Impact factor: 6.006

  7 in total

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