van Dongen M J, Doreleijers J F, van der Marel G A, van Boom J H, Hilbers C W, Wijmenga S S
NSR Centre for Molecular Structure, Design, and Synthesis, Laboratory of Biophysical Chemistry, University of Nijmegen, The Netherlands.
Nat Struct Biol. 1999 Sep;6(9):854-9. doi: 10.1038/12313.
H-DNA, thought to play a regulatory role in transcription, exists in two isomeric forms, H-y3 and H-y5. We present the first solution structure of a DNA fragment representing the H-y5 fold. The structure shows the H-y5 triple helix, and for the first time how in an H-DNA isomer the purine strand extension interacts with the triplex loop. It gives direct insight into the mechanism of H-DNA formation, and explains a host of biochemical and biophysical data on the relative stability of the H-DNA isomers. In addition, the observed interaction of the purine strand extension and the triplex loop provides new clues to the design of clamp-type triple helix-forming oligonucleotides.
H-DNA被认为在转录过程中发挥调控作用,它以两种异构体形式存在,即H-y3和H-y5。我们展示了代表H-y5折叠的DNA片段的首个溶液结构。该结构展示了H-y5三链螺旋,并且首次揭示了在H-DNA异构体中嘌呤链延伸如何与三链环相互作用。它为H-DNA形成机制提供了直接的见解,并解释了大量关于H-DNA异构体相对稳定性的生化和生物物理数据。此外,观察到的嘌呤链延伸与三链环的相互作用为钳型三链螺旋形成寡核苷酸的设计提供了新线索。