Washington: A human cell contains around 2 metres of DNA, which contains an individual's important genetic information. If all the DNA contained within a single person were unwound and stretched out, it would cover an astonishing distance - enough to reach the sun and back 60 times over. The cell compacts its DNA into densely packed chromosomes in order to manage such a massive amount of biological information.
"Imagine DNA as a piece of paper upon which all our genetic information is written." Said Minke A.D. Nijenhuis, co-corresponding author. "The paper is folded into a very tight structure in order to fit all of that information into a small cell nucleus. To read the information, however, parts of the paper have to be unfolded and then refolded. This spatial organization of our genetic code is a central mechanism of life. We therefore wanted to create a methodology that allows researchers to engineer and study the compaction of double-stranded DNA."
Natural DNA is frequently double-stranded, with one strand encoding the genes and one strand acting as a backup, interwoven in a double helix. Watson-Crick interactions, which allow the two strands to recognise and pair with one another, stabilise the double helix. However, there is another, lesser-known class of DNA interactions. These contacts, known as normal or reverse Hoogsteen interactions, allow a third strand to join in, resulting in a stunning triple helix.
In a recent paper, published in Advanced Materials, researchers from the Gothelf lab debut a general method to organize double-stranded DNA, based on Hoogsteen interactions. The study unambiguously demonstrates that triplex-forming strands are capable of sharply bending or "folding" double-stranded DNA to create compacted structures. The appearance of these structures range from hollow two-dimensional shapes to dense 3D constructs and everything in-between, including a structure resembling a potted flower. Gothelf and co-workers have named their method triplex origami.
With triplex origami, scientists can achieve a level of artificial control over the shape of double-stranded DNA that was previously unimaginable, thereby opening new avenues of exploration. It has recently been suggested that triplex formation plays a role in the natural compaction of genetic DNA and the current study may offer insight into this fundamental biological process. The work also demonstrates that the Hoogsteen-mediated triplex formation shields the DNA against enzymatic degradation. Hence, the ability to compact and protect DNA with the triplex origami method may have large implications for gene therapy, wherein diseased cells are repaired by encoding a function that they are missing into a deliverable piece of double-stranded DNA.
This biological marvel of DNA sequence and structure has also been applied in nanoscale materials engineering, yielding applications in therapeutics, diagnostics, and many other areas. "For the past four decades, DNA nanotechnology has almost exclusively relied on Watson-Crick base interactions to pair up single DNA strands and organize them into custom nanostructures." Says Professor Kurt V. Gothelf. "We now know that Hoogsteen interactions have the same potential to organize double-stranded DNA, which presents a significant conceptual expansion for the field."
Gothelf and co-workers demonstrated that Hoogsteen-mediated folding is compatible with state-of-the-art Watson-Crick-based methods. Due to the comparative rigidity of double-stranded DNA, however, triplex origami structures require fewer starting materials. This allows larger structures to be formed at a significantly lower cost. The new method has the limitation that triplex formation typically requires long stretches of purine bases within the double-stranded DNA and the researchers have therefore used artificial DNA sequences, instead of natural genetic DNA. However, in the future, they will work towards overcoming this limitation. —ANI
