Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements.

Expanded blocks of repeating nucleotide triplets have been found in or near genes associated with several human diseases. In the case of myotonic dystrophy, a block of repeating CTG trinucleotides is located downstream of the gene, and expansions of this block to repeats of n = 100 or more are frequently found in afflicted individuals. Using electron microscopy, we recently demonstrated that these blocks form unusually stable nucleosomes. Here, competitive nucleosome reconstitution was employed to measure the energetics of nucleosome formation over CTG repeat blocks of n = 75 and n = 130. These values were compared to the Xenopus borealis somatic 5S RNA gene, previously one of the strongest known natural nucleosome positioning elements. It is shown that DNA fragments containing 75 and 130 CTG repeats are 6 and 9 times stronger in nucleosome formation, respectively, than the 5S RNA gene. These findings suggest that expanded CTG blocks may profoundly alter local chromatin structure.

[1]  V. Funanage,et al.  Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy. , 1993, Genomics.

[2]  D. Nelson,et al.  Triplet repeat mutations in human disease. , 1992, Science.

[3]  T. Cech,et al.  Coaxially stacked RNA helices in the catalytic center of the Tetrahymena ribozyme. , 1994, Science.

[4]  J. Gottesfeld DNA sequence-directed nucleosome reconstitution on 5S RNA genes of Xenopus laevis , 1987, Molecular and cellular biology.

[5]  Huda Y. Zoghbi,et al.  Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1 , 1993, Nature Genetics.

[6]  C. Amemiya,et al.  Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. , 1992, Science.

[7]  K. Fischbeck,et al.  Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy , 1991, Nature.

[8]  T. Ashizawa,et al.  An unstable triplet repeat in a gene related to myotonic muscular dystrophy. , 1992, Science.

[9]  O. Onodera,et al.  Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) , 1994, Nature Genetics.

[10]  D M Crothers,et al.  Artificial nucleosome positioning sequences. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[11]  R. Wells,et al.  Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene. , 1994, Science.

[12]  A. Wolffe,et al.  A bacteriophage RNA polymerase transcribes through a Xenopus 5S RNA gene transcription complex without disrupting it , 1986, Cell.

[13]  R. Richards,et al.  Heritable unstable DNA sequences , 1992, Nature Genetics.

[14]  A. Wolffe,et al.  The structure of DNA in a nucleosome. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[15]  R I Richards,et al.  Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n , 1991, Science.

[16]  Manish S. Shah,et al.  A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes , 1993, Cell.

[17]  Jack D. Griffith,et al.  The terminus of SV40 DNA replication and transcription contains a sharp sequence-directed curve , 1988, Cell.