Scientists have recorded evidence of the brain turning off its memory inhibitor to make new memories.
In 1953, a man named Henry Molaison underwent a surgery which removed most of his hippocampus in an attempt to cure his epileptic seizures. The surgery was a qualified success though, because in addition to curing him of seizures he also lost the ability to form new long term memories. It was Molaison’s memory problems that led doctors to conclude that the hippocampus was the part of the brain responsible for long term memory.
Since then, the hippocampus has been studied frequently and it is generally accepted that it plays an important role in memory. What haven’t been studied enough are the physical processes that occur when new memories form. Scientists at the IBS Center for RNA Research and Department of Biological Sciences at Seoul National University in South Korea have discovered multiple repressive mechanisms in the hippocampus during memory formation and published their findings in this month’s issue of Science.
IBS Center for RNA Research used a tool called Ribosome profiling (RPF) as well as RNA-seq to analyze mouse hippocampi. In contrast to the widely held belief that memory formation relies on protein formation in the brain, the research group found that the genes encoding hippocampal ribosomal subunits, the organelle responsible for translating mRNA into protein, are translationally suppressed. Additionally, they found that hippocampal levels of translating ribosomes are much lower than those from other organs (livers, testes and kidneys).
They carried out RPF and RNA-seq with the mouse hippocampi after contextual fear conditioning by comparing them to an untested control group after 5,10 and 30 minutes and 4 hours post-conditioning. Through the analysis of the data, the research offers insight into translational and transcriptional regulations in the brain during memory formation at the genomic scale. The observations showed two types of repressive events were induced after learning: an initial wave of transient translational regulation at around 5 to 10 minutes and the suppression of genes through decreases of mRNA levels after 30 minutes, which continued through 4 hours.
Why did this happen? It seems that in order to make new memories, the brain needs to turn off genetic processes which act to inhibit memories from being formed. IBS researcher Jun Cho explains, “Some of these genes might be ‘memory suppressor genes’ that need to be down-regulated for memory formation.” After analyses it was found that Nrsn1, one of the newly identified genes undergoing rapid translational repression, may act as a suppressor of long-term memory formation. Additionally, activating estrogen receptor ESR1 in the hippocampus also impaired memory formation.
When an animal experiences no stimulus in an environment the hippocampus undergoes gene repression which prevents the formation of new memories. Upon the introduction of a stimulus, the hippocampus’ repressive gene regulation is turned off allowing for new memory creation, and as Jun Cho puts it, “Our study illustrates the potential importance of negative gene regulation in learning and memory”.
This work wouldn’t have been possible without the use of RPF, which allows sensitive and quantitative measurement of translation at the genomic scale. RPF yields quantitative information about the mRNAs undergoing translation and this was the first time it was used for an application involving the brain and memory formation. In the future, RPF could be used in other applications in order to gain a greater understanding of translation. More than anything else, this research highlights that new approaches need to be taken to understand the yet-unappreciated gene-regulatory events during memory formation.