scholarly journals Role of DNA Methylation in Mechanisms of Anterograde Amnesia

Author(s):  
Svetlana Solntseva ◽  
Vladimir Nikitin ◽  
Sergey Kozyrev ◽  
Pavel Nikitin

Abstract Previously, we found that impairment of conditioned food aversion memory consolidation or reconsolidation in snails by NMDA glutamate receptors antagonists led to the induction of amnesia changing over time. In particular, at the later amnesia stages (10 or more days), repeated aversion training for the same food type that was used in the initial training did not induce long-term memory formation. In these animals, long-term aversion memory for a new food type was formed. We characterized this amnesia as specific anterograde amnesia. In the present work, using DNA methyltransferases (DNMT) inhibitors, the DNA methylation processes role in mechanisms of anterograde amnesia and recovery from amnesia was investigated. It was found that in amnestic animals, DNMT inhibitor administration before or after repeated training led to the rapid long-term conditioned food aversion memory formation. It depended on proteins and mRNA synthesis at certain time windows. Thus, protein synthesis inhibitors administration before or immediately after repeated training, or RNA synthesis inhibitor injection after training, prevented memory formation induced by the DNMT inhibitor. The effects of DNMT inhibitors were specific for certain conditioned stimulus, since these inhibitors did not affect amnestic animals training for a new food stimulus. DNMT inhibition during second training removed blockade of these genes' expression, opening up access to them for transcription factors synthesized during training. Thus, this work was the first to study the molecular mechanisms of anterograde amnesia, as well as memory recovery, which can be important for search for pharmacological correction of this neuropsychic pathology.

2014 ◽  
Vol 156 (4) ◽  
pp. 430-434 ◽  
Author(s):  
S. V. Solntseva ◽  
T. S. Filatova ◽  
P. V. Nikitin ◽  
D. V. Bredov ◽  
S. A. Kozyrev ◽  
...  

2019 ◽  
Author(s):  
Kristine E. Zengeler ◽  
Caroline P. Gettens ◽  
Hannah C. Smith ◽  
Mallory M. Caron ◽  
Xinyuan Zhang ◽  
...  

SummaryDespite being fully differentiated, DNA methylation is dynamically regulated in post-mitotic glutamatergic neurons in the CA1 of the hippocampus through competing active DNA methylation and de-methylation, a process that regulates neuronal plasticity. Active DNA methylation after learning is necessary for long-term memory formation, and active DNA de-methylation by the TET enzymes has been implicated as a counter-regulator of that biochemical process. We demonstrate that Tet2 functions in the CA1 as a negative regulator of long-term memory, whereby its knockdown across the CA1 or haploinsufficiency in glutamatergic neurons enhances the fidelity of hippocampal-dependent spatial and associative memory. Loci of altered DNA methylation were then determined using whole genome bisulfite sequencing from glutamatergic Tet2 haploinsufficient CA1 tissue, which revealed hypermethylation in the promoters of genes known to be transcriptionally regulated after experiential learning. This study demonstrates a link between Tet2 activity at genes important for memory formation in CA1 glutamatergic neurons and memory fidelity.


2016 ◽  
Author(s):  
Stephanie D Biergans ◽  
Charles Claudianos ◽  
Judith Reinhard ◽  
C Giovanni Galizia

AbstractThe activity of the epigenetic writers DNA methyltransferases (Dnmts) after olfactory reward conditioning is important for both stimulus-specific long-term memory (LTM) formation and extinction. It, however, remains unknown which components of memory formation Dnmts regulate (e.g. associative vs. non-associative) and in what context (e.g. varying training conditions). Here we address these aspects in order to clarify the role of Dnmt-mediated DNA methylation in memory formation. We used a pharmacological Dnmt inhibitor and classical appetitive conditioning in the honeybee Apis mellifera, a well characterized model for classical conditioning. We quantified the effect of DNA methylation on naïve odour and sugar responses, and on responses following olfactory reward conditioning. We show that (1) Dnmts do not influence naïve odour or sugar responses, (2) Dnmts do not affect the learning of new stimuli, but (3) Dnmts influence odour-coding, i.e. 'correct' (stimulus-specific) LTM formation. Particularly, Dnmts reduce memory specificity when experience is low (one-trial training), and increase memory specificity when experience is high (multiple-trial training), generating an ecologically more useful response to learning. (4) In reversal learning conditions, Dnmts are involved in regulating both excitatory (re-acquisition) and inhibitory (forgetting) processes.


2020 ◽  
Author(s):  
Larissa N. Grinkevich

Relevance. The studies of the epigenetic mechanisms of long-term memory formation (LTM) has attracted the attention of many world leading laboratories since gained knowledge can be applied to correct cognitive impairments. miRNA dependent suppression of gene expression is the most complicated step in the epigenetic regulation, associated with a huge number of miRNAs (tens of thousands) and the diversity of their targets, thus the knowledge of miRNAs functions during LTM is still very fragmented. Aim. The aim of this study was to investigate the involvement of miRNAs in the formation of long-term memory using the model of the food aversion conditioned reflex development in the mollusk Helix. Prevention of the formation of mature miRNAs via Poly-L-lysine hydrobromide (PLL) treatment - inhibitor of Dicer activity was used as the main approach. Materials and methods. PLL was injected into animals during training, or 1, 3 or 5 hours after training. Success of the formation of conditioned reflexes was tested 72 hours after training. Results. There was a significant deterioration in LTM in animals with injected PLL 1 and 3 hours after training procedure compared with trained animals that were not injected with PLL. The treatment with PLL during training, or 5 hours after training, had no effect on LTM. Conclusion. Treatment with PLL, inhibitor of miRNA biogenesis disrupts formation of the food aversion reflex in Helix. Thus, miNRAs are involved in the LTM formation on Helix. Impaired expression of miRNAs is critical for the long-term memory formation if occurs in the intervals of 1 to 3 hours after training. We can recommend PLL for the investigations in the area of the epigenetic mechanisms of long-term memory.


2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Stephanie D. Biergans ◽  
C. Giovanni Galizia ◽  
Judith Reinhard ◽  
Charles Claudianos

Abstract DNA methylation and demethylation are epigenetic mechanisms involved in memory formation. In honey bees DNA methyltransferase (Dnmt) function is necessary for long-term memory to be stimulus specific (i.e. to reduce generalization). So far, however, it remains elusive which genes are targeted and what the time-course of DNA methylation is during memory formation. Here, we analyse how DNA methylation affects memory retention, gene expression and differential methylation in stimulus-specific olfactory long-term memory formation. Out of 30 memory-associated genes investigated here, 9 were upregulated following Dnmt inhibition in trained bees. These included Dnmt3 suggesting a negative feedback loop for DNA methylation. Within these genes also the DNA methylation pattern changed during the first 24 hours after training. Interestingly, this was accompanied by sequential activation of the DNA methylation machinery (i.e. Dnmts and Tet). In sum, memory formation involves a temporally complex epigenetic regulation of memory-associated genes that facilitates stimulus specific long-term memory in the honey bee.


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