Repeat Associated Non-ATG Translation Initiation: One DNA, Two Transcripts, Seven Reading Frames, Potentially Nine Toxic Entities!
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[1] C. E. Pearson,et al. Repeat instability as the basis for human diseases and as a potential target for therapy , 2010, Nature Reviews Molecular Cell Biology.
[2] N. Oleinick. Initiation and elongation of protein synthesis in growing cells: differential inhibition by cycloheximide and emetine. , 1977, Archives of biochemistry and biophysics.
[3] C. E. Pearson. FSHD: A Repeat Contraction Disease Finally Ready to Expand (Our Understanding of Its Pathogenesis) , 2010, PLoS genetics.
[4] B. Oostra,et al. FMR1: a gene with three faces. , 2009, Biochimica et biophysica acta.
[5] T. Ebner,et al. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8 , 2006, Nature Genetics.
[6] G. Coetzee,et al. The CAG and GGC microsatellites of the androgen receptor gene are in linkage disequilibrium in men with prostate cancer. , 1995, Cancer research.
[7] M. Hayden,et al. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing. , 1994, Human molecular genetics.
[8] H. Smeets,et al. Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients. , 2010, Human molecular genetics.
[9] G. Rouleau,et al. Molecular mechanisms underlying polyalanine diseases , 2009, Neurobiology of Disease.
[10] Radim Mazanec,et al. Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene , 2009, American journal of medical genetics. Part A.
[11] Daniel G. Miller,et al. A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy , 2010, Science.
[12] B. Brais,et al. CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation. , 2000, Human molecular genetics.
[13] D. Chitayat,et al. Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues. , 2011, Human molecular genetics.
[14] J. Taylor,et al. Repeat expansion disease: progress and puzzles in disease pathogenesis , 2010, Nature Reviews Genetics.
[15] M. Swanson,et al. Pathogenic RNAs in microsatellite expansion disease , 2009, Neuroscience Letters.
[16] S. Warren,et al. Translational suppression by trinucleotide repeat expansion at FMR1 , 1995, Science.
[17] M. Kozak,et al. Circumstances and mechanisms of inhibition of translation by secondary structure in eucaryotic mRNAs , 1989, Molecular and cellular biology.
[18] A. Prats,et al. Generation of protein isoform diversity by alternative initiation of translation at non‐AUG codons , 2003, Biology of the cell.
[19] J. Whisstock,et al. Functional insights from the distribution and role of homopeptide repeat-containing proteins. , 2005, Genome research.
[20] K. Merienne,et al. SCA8 CAG/CTG Expansions, a Tale of Two TOXICities: A Unique or Common Case? , 2009, PLoS genetics.
[21] S Karlin,et al. Trinucleotide repeats and long homopeptides in genes and proteins associated with nervous system disease and development. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[22] S. Mirkin,et al. Expansion of the (CTG)(n) repeat in the 5'-UTR of a reporter gene impedes translation. , 2000, Nucleic acids research.
[23] Daniel G. Miller,et al. Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene , 2010, PLoS genetics.
[24] D. Chitayat,et al. Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus , 2010, Nature Structural &Molecular Biology.
[25] T. Ebner,et al. RNA Gain-of-Function in Spinocerebellar Ataxia Type 8 , 2009, PLoS genetics.
[26] A. Hinnebusch,et al. Regulation of Translation Initiation in Eukaryotes: Mechanisms and Biological Targets , 2009, Cell.
[27] D. Rubinsztein,et al. Polyalanine and polyserine frameshift products in Huntington’s disease , 2006, Journal of Medical Genetics.
[28] Tilman Schneider-Poetsch,et al. Inhibition of Eukaryotic Translation Elongation by Cycloheximide and Lactimidomycin , 2010, Nature chemical biology.
[29] Brian B. Gibbens,et al. Non-ATG–initiated translation directed by microsatellite expansions , 2010, Proceedings of the National Academy of Sciences.
[30] M. Swanson,et al. Partners in crime: bidirectional transcription in unstable microsatellite disease. , 2010, Human molecular genetics.
[31] R. Reilmann,et al. Decreased plasma alanine and isoleucine in Huntington's disease , 1995, Acta neurologica Scandinavica.
[32] T. Bird,et al. SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance. , 2000, Human molecular genetics.
[33] Abel Rodríguez,et al. Early Onset Prion Disease from Octarepeat Expansion Correlates with Copper Binding Properties , 2009, PLoS pathogens.
[34] E. Jan. Divergent IRES elements in invertebrates. , 2006, Virus research.
[35] K. Sobczak,et al. CAG Repeats Containing CAA Interruptions Form Branched Hairpin Structures in Spinocerebellar Ataxia Type 2 Transcripts* , 2005, Journal of Biological Chemistry.
[36] N. Bonini,et al. RNA toxicity is a component of ataxin-3 degeneration in Drosophila , 2008, Nature.
[37] P. Hagerman,et al. Initiation of translation of the FMR1 mRNA Occurs predominantly through 5'-end-dependent ribosomal scanning. , 2011, Journal of molecular biology.