Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783673916151037952 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8016736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT bertostefano geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT fontenotmilesr geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT segersarah geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT ayhanfatma geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT caglayanemre geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT kulkarniashwinikumar geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT douglasconnor geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT tammingacarola geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT legabradleyc geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding AT konopkagenevieve geneexpressioncorrelatesoftheoscillatorysignaturessupportinghumanepisodicmemoryencoding |