Related Content
Search Google Scholar for:
|
|
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
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 »
|
|