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Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding

In humans, brain oscillations support critical features of memory formation. However, understanding the molecular mechanisms underlying this activity remains a major challenge. We measured memory-sensitive oscillations using intracranial electroencephalography recordings from the temporal cortex of...

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Autores principales: Berto, Stefano, Fontenot, Miles R., Seger, Sarah, Ayhan, Fatma, Caglayan, Emre, Kulkarni, Ashwinikumar, Douglas, Connor, Tamminga, Carol A., Lega, Bradley C., Konopka, Genevieve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016736/
https://www.ncbi.nlm.nih.gov/pubmed/33686299
http://dx.doi.org/10.1038/s41593-021-00803-x
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author Berto, Stefano
Fontenot, Miles R.
Seger, Sarah
Ayhan, Fatma
Caglayan, Emre
Kulkarni, Ashwinikumar
Douglas, Connor
Tamminga, Carol A.
Lega, Bradley C.
Konopka, Genevieve
author_facet Berto, Stefano
Fontenot, Miles R.
Seger, Sarah
Ayhan, Fatma
Caglayan, Emre
Kulkarni, Ashwinikumar
Douglas, Connor
Tamminga, Carol A.
Lega, Bradley C.
Konopka, Genevieve
author_sort Berto, Stefano
collection PubMed
description In humans, brain oscillations support critical features of memory formation. However, understanding the molecular mechanisms underlying this activity remains a major challenge. We measured memory-sensitive oscillations using intracranial electroencephalography recordings from the temporal cortex of patients performing an episodic memory task. When these patients undergo resection subsequently, we employ transcriptomics on the temporal cortex to link gene expression with brain oscillations, identifying genes correlated with oscillatory signatures of memory formation across six frequency bands. A co-expression analysis isolated oscillatory signature-specific modules associated with neuropsychiatric disorders as well as ion channel activity, with highly correlated genes exhibiting strong connectivity within these modules. Using single-nuclei transcriptomics, we further revealed that these modules are enriched for specific classes of both excitatory and inhibitory neurons, and immunohistochemistry confirmed expression of highly correlated genes. This unprecedented dataset of patient-specific brain oscillations coupled to genomics unlocks new insights into the genetic mechanisms that support memory encoding.
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spelling pubmed-80167362021-09-08 Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding Berto, Stefano Fontenot, Miles R. Seger, Sarah Ayhan, Fatma Caglayan, Emre Kulkarni, Ashwinikumar Douglas, Connor Tamminga, Carol A. Lega, Bradley C. Konopka, Genevieve Nat Neurosci Article In humans, brain oscillations support critical features of memory formation. However, understanding the molecular mechanisms underlying this activity remains a major challenge. We measured memory-sensitive oscillations using intracranial electroencephalography recordings from the temporal cortex of patients performing an episodic memory task. When these patients undergo resection subsequently, we employ transcriptomics on the temporal cortex to link gene expression with brain oscillations, identifying genes correlated with oscillatory signatures of memory formation across six frequency bands. A co-expression analysis isolated oscillatory signature-specific modules associated with neuropsychiatric disorders as well as ion channel activity, with highly correlated genes exhibiting strong connectivity within these modules. Using single-nuclei transcriptomics, we further revealed that these modules are enriched for specific classes of both excitatory and inhibitory neurons, and immunohistochemistry confirmed expression of highly correlated genes. This unprecedented dataset of patient-specific brain oscillations coupled to genomics unlocks new insights into the genetic mechanisms that support memory encoding. 2021-03-08 2021-04 /pmc/articles/PMC8016736/ /pubmed/33686299 http://dx.doi.org/10.1038/s41593-021-00803-x Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Berto, Stefano
Fontenot, Miles R.
Seger, Sarah
Ayhan, Fatma
Caglayan, Emre
Kulkarni, Ashwinikumar
Douglas, Connor
Tamminga, Carol A.
Lega, Bradley C.
Konopka, Genevieve
Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding
title Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding
title_full Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding
title_fullStr Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding
title_full_unstemmed Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding
title_short Gene expression correlates of the oscillatory signatures supporting human episodic memory encoding
title_sort gene expression correlates of the oscillatory signatures supporting human episodic memory encoding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016736/
https://www.ncbi.nlm.nih.gov/pubmed/33686299
http://dx.doi.org/10.1038/s41593-021-00803-x
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