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Title: Monovalent cation induced structural transitions in telomeric DNAs: G-DNA folding intermediates

Journal Article · · Biochemistry; (United States)
DOI:https://doi.org/10.1021/bi00232a013· OSTI ID:5393126
;  [1];  [2];  [3]
  1. North Carolina State Univ., Raleigh (USA)
  2. Iowa State Univ., Ames (USA)
  3. Univ. of California, Berkeley (USA)

Telomeric DNA consists of G- and C-rich strands that are always polarized such that the G-rich strand extends past the 3{prime} end of the duplex to form a 12-16-base overhang. These overhanging strands can self-associate in vitro to form intramolecular structures that have several unusual physical properties and at least one common feature, the presence of non-Watson-Crick G{center dot}G base pairs. The term G-DNA was coined for this class of structures. On the basis of gel electrophoresis, imino proton NMR, and circular dichroism (CD) results, the authors find that changing the counterions from sodium to potassium specifically induces conformational transitions in the G-rich telomeric DNA from Tetrahymena, d(T{sub 2}G{sub 4}){sub 4} (TET4), which results in a change from the intramolecular species to an apparent multistranded structure, accompanied by an increase in the melting temperature of the base pairs of >25{degree}, as monitored by loss of the imino proton NMR signals. They infer that the multistranded structure is a quadruplex. The results indicate that specific differences in ionic interactions can result in a switch in telomeric DNAs between intramolecular hairpin-like or quadruplex-containing species and intermolecular quadruplex structures, all of which involve G{center dot}G base pairing interaction. They propose a model in which duplex or hairpin forms of G-DNA are folding intermediates in the formation of either 1-, 2-, or 4-stranded quadruplex structures.

DOE Contract Number:
FG03-86ER60406
OSTI ID:
5393126
Journal Information:
Biochemistry; (United States), Vol. 30:18; ISSN 0006-2960
Country of Publication:
United States
Language:
English