Molecular Mechanisms for Changing Brain Connectivity in Mice and Humans

The goal of this study was to examine commonalities in the molecular basis of learning in mice and humans. In previous work we have demonstrated that the anterior cingulate cortex (ACC) and hippocampus (HC) are involved in learning a two-choice visuospatial discrimination task. Here, we began by loo...

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Main Authors: Pascale Voelker, Aldis P. Weible, Cristopher M. Niell, Mary K. Rothbart, Michael I. Posner
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/21/15840
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author Pascale Voelker
Aldis P. Weible
Cristopher M. Niell
Mary K. Rothbart
Michael I. Posner
author_facet Pascale Voelker
Aldis P. Weible
Cristopher M. Niell
Mary K. Rothbart
Michael I. Posner
author_sort Pascale Voelker
collection DOAJ
description The goal of this study was to examine commonalities in the molecular basis of learning in mice and humans. In previous work we have demonstrated that the anterior cingulate cortex (ACC) and hippocampus (HC) are involved in learning a two-choice visuospatial discrimination task. Here, we began by looking for candidate genes upregulated in mouse ACC and HC with learning. We then determined which of these were also upregulated in mouse blood. Finally, we used RT-PCR to compare candidate gene expression in mouse blood with that from humans following one of two forms of learning: a working memory task (network training) or meditation (a generalized training shown to change many networks). Two genes were upregulated in mice following learning: caspase recruitment domain-containing protein 6 (<i>Card6</i>) and inosine monophosphate dehydrogenase 2 (<i>Impdh2</i>). The <i>Impdh2</i> gene product catalyzes the first committed step of guanine nucleotide synthesis and is tightly linked to cell proliferation. The <i>Card6</i> gene product positively modulates signal transduction. In humans, <i>Card6</i> was significantly upregulated, and <i>Impdh2</i> trended toward upregulation with training. These genes have been shown to regulate pathways that influence nuclear factor kappa B (<i>NF-κB</i>), a factor previously found to be related to enhanced synaptic function and learning.
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spelling doaj.art-a9ec4ea97fe94882aee6d5bdb2ad28b12023-11-10T15:05:30ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-10-0124211584010.3390/ijms242115840Molecular Mechanisms for Changing Brain Connectivity in Mice and HumansPascale Voelker0Aldis P. Weible1Cristopher M. Niell2Mary K. Rothbart3Michael I. Posner4Department of Psychology, University of Oregon, Eugene, OR 97403, USAInstitute of Neuroscience, University of Oregon, Eugene, OR 97403, USAInstitute of Neuroscience, University of Oregon, Eugene, OR 97403, USADepartment of Psychology, University of Oregon, Eugene, OR 97403, USADepartment of Psychology, University of Oregon, Eugene, OR 97403, USAThe goal of this study was to examine commonalities in the molecular basis of learning in mice and humans. In previous work we have demonstrated that the anterior cingulate cortex (ACC) and hippocampus (HC) are involved in learning a two-choice visuospatial discrimination task. Here, we began by looking for candidate genes upregulated in mouse ACC and HC with learning. We then determined which of these were also upregulated in mouse blood. Finally, we used RT-PCR to compare candidate gene expression in mouse blood with that from humans following one of two forms of learning: a working memory task (network training) or meditation (a generalized training shown to change many networks). Two genes were upregulated in mice following learning: caspase recruitment domain-containing protein 6 (<i>Card6</i>) and inosine monophosphate dehydrogenase 2 (<i>Impdh2</i>). The <i>Impdh2</i> gene product catalyzes the first committed step of guanine nucleotide synthesis and is tightly linked to cell proliferation. The <i>Card6</i> gene product positively modulates signal transduction. In humans, <i>Card6</i> was significantly upregulated, and <i>Impdh2</i> trended toward upregulation with training. These genes have been shown to regulate pathways that influence nuclear factor kappa B (<i>NF-κB</i>), a factor previously found to be related to enhanced synaptic function and learning.https://www.mdpi.com/1422-0067/24/21/15840anterior cingulate cortex<i>Card6</i>hippocampusmyelinnetwork training<i>NF-κB</i>
spellingShingle Pascale Voelker
Aldis P. Weible
Cristopher M. Niell
Mary K. Rothbart
Michael I. Posner
Molecular Mechanisms for Changing Brain Connectivity in Mice and Humans
International Journal of Molecular Sciences
anterior cingulate cortex
<i>Card6</i>
hippocampus
myelin
network training
<i>NF-κB</i>
title Molecular Mechanisms for Changing Brain Connectivity in Mice and Humans
title_full Molecular Mechanisms for Changing Brain Connectivity in Mice and Humans
title_fullStr Molecular Mechanisms for Changing Brain Connectivity in Mice and Humans
title_full_unstemmed Molecular Mechanisms for Changing Brain Connectivity in Mice and Humans
title_short Molecular Mechanisms for Changing Brain Connectivity in Mice and Humans
title_sort molecular mechanisms for changing brain connectivity in mice and humans
topic anterior cingulate cortex
<i>Card6</i>
hippocampus
myelin
network training
<i>NF-κB</i>
url https://www.mdpi.com/1422-0067/24/21/15840
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