Scientists have found that a second layer of information exists on top of the genetic code in DNA, confirming a long-standing hypothesis.
Researchers at Leiden Institute of Physics in The Netherlands have proven that DNA mechanics, in addition to genetic information in DNA, determines who we are.
Leiden physicist Helmut Schiessel and his group simulated many DNA sequences and found a correlation between mechanical cues and the way DNA is folded.
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The sequence of the letters G, A, T and C in the famous double helix determines what proteins are made made within our body.
If you have brown eyes, for example, this is because a series of letters in your DNA encodes for proteins that build brown eyes. Each cell contains the exact same letter sequence, and yet every organ behaves differently.
Since the mid 1980s, it has been hypothesised that there is a second layer of information on top of the genetic code consisting of DNA mechanical properties.
Each of our cells contains two meters of DNA molecules, and these molecules need to be wrapped up tightly to fit inside a single cell.
The way in which DNA is folded determines how the letters are read out, and therefore which proteins are actually made.
In each organ, only relevant parts of the genetic information are read. The theory suggests that mechanical cues within the DNA structures determine how preferentially DNA folds.
For the first time, Schiessel and his research group provide strong evidence that this second layer of information indeed exists.
With their computer code, they have simulated the folding of DNA strands with randomly assigned mechanical cues. It turns out that these cues indeed determine how the DNA molecule is folded into so-called nucleosomes.
Schiessel found correlations between the mechanics and the actual folding structure in the genome of two organisms - baker's yeast and fission yeast.
This finding shows evolutionary changes in DNA - mutations - that have two very different effects: The letter sequence encoding for a specific protein can change, or the mechanics of the DNA structure can change, resulting in different packaging and levels of DNA accessibility, and therefore differing frequency of production of that protein.
The study was published in the journal PLoS One.