Their study confirms that the formation of memories is accompanied by an altered activity of specific genes. In addition, they found unprecedented evidence that supports the hypothesis DNA methylation may be the molecular basis of long-term memory.
The scientists stimulated long-term memory in mice, by training the animals to recognise a specific test environment. Based on tissue samples, they could discern to what extent this learning task triggered changes in the activity of the genes in the mice’s brain cells. Their focus was on epigenetic modifications. Gene regulation can happen through methylation. Changes in the histones that are packaging the DNA may also occur.
Hennion: “Research on epigenetic changes that are related to memory processes is still at an early stage. We look at such features, not only for the purpose of a better understanding of how memory works. We also look for potential targets for drugs that may counteract memory decline. Ultimately, our research is about therapies against Alzheimer’s and similar brain diseases.”
In the current study they found modifications, both of the histones as well as of the methylation of the DNA. However, histone modifications had little effect on the activity of genes involved in neuroplasticity. Furthermore, Bonn and his colleagues not only discovered epigenetic modifications in nerve cells, but also in non-neuronal cells of the brain.
“The relevance of non-neuronal cells for memory, is an interesting topic that we will continue to pursue,” says Prof. André Fischer. “Furthermore, our observations suggest that neuroplasticity is to a large extent regulated by DNA methylation. Although this is not a new hypothesis, our study provides an unprecedented amount of supporting evidence for this. Thus, methylation may indeed be an important molecular constituent of long-term memory. In such a case, methylation could be a sort of code for memory content and a potential target for therapies against Alzheimer’s disease. This is an aspect that we specifically want to focus on, in further studies.” http://www.dzne.de/en/about-us/public-relations/meldungen/2015/press-release-no-22.html
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