Substitution of adenine for guanine in the quadruplex-forming human telomere DNA sequence G(3)(T(2)AG(3))(3)
Language English Country France Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18852018
DOI
10.1016/j.biochi.2008.07.012
PII: S0300-9084(08)00231-9
Knihovny.cz E-resources
- MeSH
- Adenine chemistry MeSH
- Circular Dichroism MeSH
- DNA chemistry MeSH
- G-Quadruplexes * MeSH
- Guanine chemistry MeSH
- Nucleic Acid Conformation MeSH
- Humans MeSH
- Base Sequence MeSH
- Telomere chemistry MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Adenine MeSH
- DNA MeSH
- Guanine MeSH
We have studied the formation and structural properties of quadruplexes of the human telomeric DNA sequence G(3)(T(2)AG(3))(3) and related sequences in which each guanine base was replaced by an adenine base. None of these single base substitutions hindered the formation of antiparallel quadruplexes, as shown by circular dichroism, gel electrophoresis, and UV thermal stability measurements in NaCl solutions. Effect of substitution did differ, however, depending on the position of the substituted base. The A-for-G substitution in the middle quartet of the antiparallel basket scaffold led to the most distorted and least stable structures and these sequences preferred to form bimolecular quadruplexes. Unlike G(3)(T(2)AG(3))(3), no structural transitions were observed for the A-containing analogs of G(3)(T(2)AG(3))(3) when sodium ions were replaced by potassium ions. The basic quadruplex topology remained the same for all sequences studied in both salts. As in vivo misincorporation of A for a G in the telomeric sequence is possible and potassium is a physiological salt, these findings may have biological relevance.
References provided by Crossref.org
i-Motif of cytosine-rich human telomere DNA fragments containing natural base lesions
Altered biochemical specificity of G-quadruplexes with mutated tetrads
Loss of loop adenines alters human telomere d[AG3(TTAG3)3] quadruplex folding