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CGG repeats associated with fragile X chromosome form left-handed Z-DNA structure
D. Renčiuk, J. Kypr, M. Vorlíčková
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Wiley Online Library (archiv)
from 1996-01-01 to 2012-12-31
Wiley Online Library (archiv)
from 1996-01-01 to 2012-12-31
PubMed
20960567
DOI
10.1002/bip.21555
Knihovny.cz E-resources
- MeSH
- Circular Dichroism MeSH
- Chromosome Fragile Sites genetics MeSH
- Nucleic Acid Conformation MeSH
- Humans MeSH
- Chromosomes, Human, X genetics MeSH
- Base Sequence MeSH
- Fragile X Syndrome genetics MeSH
- Trinucleotide Repeats MeSH
- DNA, Z-Form chemistry genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
This work is a continuation of our effort to determine the structure responsible for expansion of the (CGG)(n) motif that results in fragile X chromosome syndrome. In our previous report, we demonstrated that the structure adopted by an oligonucleotide with this repeat sequence is not a quadruplex as was suggested by others. Here we demonstrate that (CGG) runs adopt another anomalous arrangement-a left-handed Z-DNA structure. The Z-DNA formation was induced by high salt and millimolar concentrations of Ni(2+) ions and likelihood of its formation increased with increasing number of repeats. In an oligonucleotide in which the CGG runs were interrupted by AGG triplets, as is observed in genomes of healthy individuals, the hairpin conformation was stabilized and Z-DNA formation was hindered. We show here that methylation of the (CGG) runs markedly stabilized Z-DNA formation. We hypothesize that rather than in the expansion process the Z-DNA may be formed by long, expanded (CGG) stretches that become hypermethylated; this would inhibit transcription resulting in disease.
References provided by Crossref.org
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