Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 29 July 1994:
Vol. 265. no. 5172, pp. 669 - 671
DOI: 10.1126/science.8036515

Articles

Science, Vol 265, Issue 5172, 669-671
Copyright © 1994 by American Association for the Advancement of Science


articles

Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene

YH Wang, S Amirhaeri, S Kang, RD Wells, and JD Griffith

Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill 27599.

The expansion of CTG repeats in DNA occurs in or near genes involved in several human diseases, including myotonic dystrophy and Huntington's disease. Nucleosomes, the basic structural element of chromosomes, consist of 146 base pairs of DNA coiled about an octamer of histone proteins and mediate general transcriptional repression. Electron microscopy was used to examine in vitro the nucleosome assembly of DNA containing repeating CTG triplets. The efficiency of nucleosome formation increased with expanded triplet blocks, suggesting that such blocks may repress transcription through the creation of stable nucleosomes.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Comparative Genomics and Molecular Dynamics of DNA Repeats in Eukaryotes.
G.-F. Richard, A. Kerrest, and B. Dujon (2008)
Microbiol. Mol. Biol. Rev. 72, 686-727
   Abstract »    Full Text »    PDF »
Long intronic GAA*TTC repeats induce epigenetic changes and reporter gene silencing in a molecular model of Friedreich ataxia.
E. Soragni, D. Herman, S. Y. R. Dent, J. M. Gottesfeld, R. D. Wells, and M. Napierala (2008)
Nucleic Acids Res. 36, 6056-6065
   Abstract »    Full Text »    PDF »
DNA triplexes and Friedreich ataxia.
R. D. Wells (2008)
FASEB J 22, 1625-1634
   Abstract »    Full Text »    PDF »
Effect of Sequence-Directed Nucleosome Disruption on Cell-Type-Specific Repression by {alpha}2/Mcm1 in the Yeast Genome.
N. Morohashi, Y. Yamamoto, S. Kuwana, W. Morita, H. Shindo, A. P. Mitchell, and M. Shimizu (2006)
Eukaryot. Cell 5, 1925-1933
   Abstract »    Full Text »    PDF »
MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.
M. de Haro, I. Al-Ramahi, B. De Gouyon, L. Ukani, A. Rosa, N. A. Faustino, T. Ashizawa, T. A. Cooper, and J. Botas (2006)
Hum. Mol. Genet. 15, 2138-2145
   Abstract »    Full Text »    PDF »
A High Mobility Group Protein Binds to Long CAG Repeat Tracts and Establishes Their Chromatin Organization in Saccharomyces cerevisiae.
H. Kim and D. M. Livingston (2006)
J. Biol. Chem. 281, 15735-15740
   Abstract »    Full Text »    PDF »
Effect of CAT or AGG Interruptions and CpG Methylation on Nucleosome Assembly upon Trinucleotide Repeats on Spinocerebellar Ataxia, Type 1 and Fragile X Syndrome.
D. J. Mulvihill, K. N. Edamura, K. A. Hagerman, C. E. Pearson, and Y.-H. Wang (2005)
J. Biol. Chem. 280, 4498-4503
   Abstract »    Full Text »    PDF »
A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation.
J. J. Higgins, J. Pucilowska, R. Q. Lombardi, and J. P. Rooney (2004)
Neurology 63, 1927-1931
   Abstract »    Full Text »    PDF »
Trinucleotide repeats and neurodegenerative disease.
C. M. Everett and N. W. Wood (2004)
Brain 127, 2385-2405
   Abstract »    Full Text »    PDF »
Molecular Genetics of Human Cognition.
E. J. Weeber, J. M. Levenson, and J. D. Sweatt (2002)
Mol. Interv. 2, 376-391
   Abstract »    Full Text »    PDF »
A Relationship Between Lengths of Microsatellites and Nearby Substitution Rates in Mammalian Genomes.
M. F. Santibanez-Koref, R. Gangeswaran, and J. M. Hancock (2001)
Mol. Biol. Evol. 18, 2119-2123
   Full Text »    PDF »
Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite.
V. Albanese, N. F. Biguet, H. Kiefer, E. Bayard, J. Mallet, and R. Meloni (2001)
Hum. Mol. Genet. 10, 1785-1792
   Abstract »    Full Text »    PDF »
Nucleosome Structural Features and Intrinsic Properties of the TATAAACGCC Repeat Sequence.
H. R. Widlund, P. N. Kuduvalli, M. Bengtsson, H. Cao, T. D. Tullius, and M. Kubista (1999)
J. Biol. Chem. 274, 31847-31852
   Abstract »    Full Text »    PDF »
Genetic Instabilities in (CTG{middle dot}CAG) Repeats Occur by Recombination.
J. P. Jakupciak and R. D. Wells (1999)
J. Biol. Chem. 274, 23468-23479
   Abstract »    Full Text »    PDF »
DNA secondary structure: A common and causative factor for expansion in human disease.
C. T. McMurray (1999)
PNAS 96, 1823-1825
   Full Text »    PDF »
Expansion and Deletion of Triplet Repeat Sequences in Escherichia coli Occur on the Leading Strand of DNA Replication.
R. R. Iyer and R. D. Wells (1999)
J. Biol. Chem. 274, 3865-3877
   Abstract »    Full Text »    PDF »
Transcriptional Properties of RNA Polymerase II within Triplet Repeat-containing DNA from the Human Myotonic Dystrophy and Fragile X Loci.
M. A. Parsons, R. R. Sinden, and M. G. Izban (1998)
J. Biol. Chem. 273, 26998-27008
   Abstract »    Full Text »    PDF »
Myotonic Dystrophy as a Brain Disorder.
T. Ashizawa (1998)
Arch Neurol 55, 291-293
   Full Text »    PDF »
Transcription of Human ABO Histo-blood Group Genes Is Dependent upon Binding of Transcription Factor CBF/NF-Y to Minisatellite Sequence.
Y. Kominato, T. Tsuchiya, N. Hata, H. Takizawa, and F.-i. Yamamoto (1997)
J. Biol. Chem. 272, 25890-25898
   Abstract »    Full Text »    PDF »
Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts.
B. M. Davis, M. E. McCurrach, K. L. Taneja, R. H. Singer, and D. E. Housman (1997)
PNAS 94, 7388-7393
   Abstract »    Full Text »    PDF »
Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes.
M. G. Hamshere, E. E. Newman, M. Alwazzan, B. S. Athwal, and J. D. Brook (1997)
PNAS 94, 7394-7399
   Abstract »    Full Text »    PDF »
Flexible DNA: Genetically Unstable CTG·CAG and CGG·CCG from Human Hereditary Neuromuscular Disease Genes.
A. Bacolla, R. Gellibolian, M. Shimizu, S. Amirhaeri, S. Kang, K. Ohshima, J. E. Larson, S. C. Harvey, B. D. Stollar, and R. D. Wells (1997)
J. Biol. Chem. 272, 16783-16792
   Abstract »    Full Text »    PDF »
Hairpin Formation during DNA Synthesis Primer Realignment in Vitro in Triplet Repeat Sequences from Human Hereditary Disease Genes.
K. Ohshima and R. D. Wells (1997)
J. Biol. Chem. 272, 16798-16806
   Abstract »    Full Text »    PDF »
Methylation of Expanded CCG Triplet Repeat DNA from Fragile X Syndrome Patients Enhances Nucleosome Exclusion.
Y.-H. Wang and J. Griffith (1996)
J. Biol. Chem. 271, 22937-22940
   Abstract »    Full Text »    PDF »
Cloning, Characterization, and Properties of Seven Triplet Repeat DNA Sequences.
K. Ohshima, S. Kang, J. E. Larson, and R. D. Wells (1996)
J. Biol. Chem. 271, 16773-16783
   Abstract »    Full Text »    PDF »
TTA·TAA Triplet Repeats in Plasmids Form a Non-H Bonded Structure.
K. Ohshima, S. Kang, J. E. Larson, and R. D. Wells (1996)
J. Biol. Chem. 271, 16784-16791
   Abstract »    Full Text »    PDF »
Purification of Nuclear Proteins from Human HeLa Cells That Bind Specifically to the Unstable Tandem Repeat (CGG)[IMAGE] in the Human FMR1 Gene.
H. Deissler, A. Behn-Krappa, and W. Doerfler (1996)
J. Biol. Chem. 271, 4327-4334
   Abstract »    Full Text »    PDF »
Molecular Basis of Genetic Instability of Triplet Repeats.
R. D. Wells and R. D. Wells (1996)
J. Biol. Chem. 271, 2875-2878
   Full Text »    PDF »
CTG Triplet Repeats from Human Hereditary Diseases Are Dominant Genetic Expansion Products in Escherichia coli.
K. Ohshima, S. Kang, and R. D. Wells (1996)
J. Biol. Chem. 271, 1853-1856
   Abstract »    Full Text »    PDF »
Myotonic Dystrophy: Discussion of Molecular Mechanism.
C.T. Caskey, M.S. Swanson, and L.T. Timchenko (1996)
Cold Spring Harb Symp Quant Biol 61, 607-614
   Abstract »    PDF »
The Molecular Basis of Fragile X Syndrome.
D.E. Eberhart and S.T. Warren (1996)
Cold Spring Harb Symp Quant Biol 61, 679-687
   Abstract »    PDF »
Pausing of DNA Synthesis in Vitro at Specific Loci in CTG and CGG Triplet Repeats from Human Hereditary Disease Genes.
S. Kang, K. Ohshima, M. Shimizu, S. Amirhaeri, and R. D. Wells (1995)
J. Biol. Chem. 270, 27014-27021
   Abstract »    Full Text »    PDF »
Differential Effects of Simple Repeating DNA Sequences on Gene Expression from the SV40 Early Promoter.
S. Amirhaeri, F. Wohlrab, and R. D. Wells (1995)
J. Biol. Chem. 270, 3313-3319
   Abstract »    Full Text »    PDF »
Independent Regulation of the Myotonic Dystrophy 1 Locus Genes Postnatally and during Adult Skeletal Muscle Regeneration.
M. Eriksson, T. Ansved, L. Edstrom, D. J. Wells, D. J. Watt, M. Anvret, and N. Carey (2000)
J. Biol. Chem. 275, 19964-19969
   Abstract »    Full Text »    PDF »
Gene Conversion (Recombination) Mediates Expansions of CTG{middle dot}CAG Repeats.
J. P. Jakupciak and R. D. Wells (2000)
J. Biol. Chem. 275, 40003-40013
   Abstract »    Full Text »    PDF »
Meiotic instability of CAG repeat tracts occurs by double-strand break repair in yeast.
C. Jankowski, F. Nasar, and D. K. Nag (2000)
PNAS 97, 2134-2139
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)