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CGG repeats associated with fragile X chromosome form left-handed Z-DNA structure
D. Renčiuk, J. Kypr, M. Vorlíčková
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Wiley Online Library (archiv)
od 1996-01-01 do 2012-12-31
Wiley Online Library (archiv)
od 1996-01-01 do 2012-12-31
PubMed
20960567
DOI
10.1002/bip.21555
Knihovny.cz E-zdroje
- MeSH
- cirkulární dichroismus MeSH
- fragilní místa na chromozomu genetika MeSH
- konformace nukleové kyseliny MeSH
- lidé MeSH
- lidské chromozomy X genetika MeSH
- sekvence nukleotidů MeSH
- syndrom fragilního X genetika MeSH
- trinukleotidové repetice MeSH
- Z-DNA chemie genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem 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.
Citace poskytuje Crossref.org
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