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Parallel intramolecular DNA triple helix with G and T bases in the third strand stabilized by Zn(2+) ions.
Khomyakova, E B; Gousset, H; Liquier, J; Huynh-Dinh, T; Gouyette, C; Takahashi, M; Florentiev, V L; Taillandier, E.
Afiliación
  • Khomyakova EB; Laboratoire de Spectroscopie Biomoléculaire, URA CNRS 1430, Université Paris Nord, 74 rue Marcel Cachin, F-93017 Bobigny Cedex, France.
Nucleic Acids Res ; 28(18): 3511-6, 2000 Sep 15.
Article en En | MEDLINE | ID: mdl-10982870
ABSTRACT
We present evidence of formation of an intramolecular parallel triple helix with T*A.T and G*G.C base triplets (where * represents the hydrogen bonding interaction between the third strand and the duplex while. represents the Watson-Crick interactions which stabilize the duplex). The third GT strand, containing seven GpT/TpG steps, targets the polypurine sequence 5'-AGG-AGG-GAG-GAG-3'. The triple helix is obtained by the folding back twice of a 36mer, formed by three dodecamers tethered by hydroxyalkyl linkers (-L-). Due to the design of the oligonucleotide, the third strand orientation is parallel with respect to the polypurine strand. Triple helical formation has been studied in concentration conditions in which native gel electrophoresis experiments showed the absence of intermolecular structures. Circular dichroism (CD) and UV spectroscopy have been used to evidence the triplex structure. A CD spectrum characteristic of triple helical formation as well as biphasic UV and CD melting curves have been obtained in high ionic strength NaCl solutions in the presence of Zn(2+) ions. Specific interactions with Zn(2+) ions in low water activity conditions are necessary to stabilize the parallel triplex.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Zinc / ADN Idioma: En Revista: Nucleic Acids Res Año: 2000 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Zinc / ADN Idioma: En Revista: Nucleic Acids Res Año: 2000 Tipo del documento: Article País de afiliación: Francia