Neuroscientists Discover New Molecular Mechanism for Long-Term Memory Formation

A team of researchers led by Dr Marcelo Wood from the University of California at Irvine has discovered a new molecular mechanism that helps trigger long-term memory formation.

The discovery of a new molecular mechanism that helps trigger long-term memory formation adds a piece to the puzzle in the ongoing effort to uncover the mysteries of memory (University of Minnesota)

The discovery of a new molecular mechanism that helps trigger long-term memory formation adds a piece to the puzzle in the ongoing effort to uncover the mysteries of memory (University of Minnesota)

The team investigated the role of a gene called Baf53b, also known as ACTL6B or actin-like 6B, in long-term memory formation. Baf53b is one of several proteins making up a molecular complex called nBAF.

Mutations in the proteins of the nBAF complex have been linked to several intellectual disorders, including Coffin-Siris syndrome, Nicolaides-Baraitser syndrome and sporadic autism. One of the key questions the team addressed is how mutations in components of the nBAF complex lead to cognitive impairments.

The team used mice bred with mutations in Baf53b. While this genetic modification did not affect the mice’s ability to learn, it did notably inhibit long-term memories from forming and severely impaired synaptic function.

“These findings present a whole new way to look at how long-term memories form,” said Prof Wood, who co-authored a paper in Nature Neuroscience.

“They also provide a mechanism by which mutations in the proteins of the nBAF complex may underlie the development of intellectual disability disorders characterized by significant cognitive impairments.”

How does this mechanism regulate gene expression required for long-term memory formation?

Most genes are tightly packaged by a chromatin structure – chromatin being what compacts DNA so that it fits inside the nucleus of a cell. That compaction mechanism represses gene expression. Baf53b, and the nBAF complex, physically open the chromatin structure so specific genes required for long-term memory formation are turned on. The mutated forms of Baf53b did not allow for this necessary gene expression.

“The results from this study reveal a powerful new mechanism that increases our understanding of how genes are regulated for memory formation,” Prof Wood said.

The researchers believe the discovery of this mechanism adds another piece to the puzzle in the ongoing effort to uncover the mysteries of memory and, potentially, certain intellectual disabilities.

“Our next step is to identify the key genes the nBAF complex regulates. With that information, we can begin to understand what can go wrong in intellectual disability disorders, which paves a path toward possible therapeutics.”

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Bibliographic information: Annie Vogel-Ciernia et al. The neuron-specific chromatin regulatory subunit BAF53b is necessary for synaptic plasticity and memory. Nature Neuroscience, published online 24 March 2013; doi: 10.1038/nn.3359