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Triple helical DNA in a duplex context and base pair opening
Author(s) -
Mauricio Esguerra,
Lennart Nilsson,
Alessandra Villa
Publication year - 2014
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gku848
Subject(s) - duplex (building) , base pair , triple helix , antiparallel (mathematics) , molecular structure of nucleic acids: a structure for deoxyribose nucleic acid , helix (gastropod) , dna , context (archaeology) , biology , crystallography , biophysics , physics , genetics , chemistry , ecology , paleontology , quantum mechanics , snail , magnetic field
It is fundamental to explore in atomic detail the behavior of DNA triple helices as a means to understand the role they might play in vivo and to better engineer their use in genetic technologies, such as antigene therapy. To this aim we have performed atomistic simulations of a purine-rich antiparallel triple helix stretch of 10 base triplets flanked by canonical Watson-Crick double helices. At the same time we have explored the thermodynamic behavior of a flipping Watson-Crick base pair in the context of the triple and double helix. The third strand can be accommodated in a B-like duplex conformation. Upon binding, the double helix changes shape, and becomes more rigid. The triple-helical region increases its major groove width mainly by oversliding in the negative direction. The resulting conformations are somewhere between the A and B conformations with base pairs remaining almost perpendicular to the helical axis. The neighboring duplex regions maintain a B DNA conformation. Base pair opening in the duplex regions is more probable than in the triplex and binding of the Hoogsteen strand does not influence base pair breathing in the neighboring duplex region.

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