Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus

Detalhes bibliográficos
Autor(a) principal: ILL-Raga, Gerard
Data de Publicação: 2013
Outros Autores: Kohler, Cristiano, Radiske, Andressa, Lima, Ramón H., Rosen, Mark D., Muñoz, Francisco J., Cammarota, Martín Pablo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/23295
Resumo: Local control of protein synthesis at synapses is crucial for synaptic plasticity and memory formation. However, little is known about the signals coupling neurotransmitter release with the translational machinery during these processes. Here, we studied the involvement of heme-regulated inhibitor (HRI) kinase, a kinase activated by nitric oxide that phosphorylates eukaryotic initiation factor 2α (eIF2α), in object recognition (OR) memory consolidation. Phosphorylated eIF2α mediates two opposing effects upon translation: translational arrest of most mRNAs and translational activation of selected mRNAs bearing specific features in their 5'untranslated regions (5'UTRs). We found that HRI kinase activation in the CA1 region of the dorsal hippocampus is necessary for retention of OR memory in rats. Accordingly, learning induced a transient increase in the phosphorylation state of eIF2α in dorsal CA1 which was abolished by the HRI kinase inhibitor N-(2,6-dimethylbenzyl)-6,7-dimethoxy-2H-[1]benzofuro[3,2-c]pyrazol-3-amine hydrochloride (AMI). The increase in p-eIF2α was associated with increased expression of BACE1 and activating transcription factor 4, two proteins containing eIF2α-responsive 5'UTRs in their mRNAs that play a key role in synaptic plasticity. Our data suggests that learning promotes the transient phosphorylation of eIF2α to allow for translation of specific 5'UTR-mRNAs through a process requiring HRI kinase activation.
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spelling ILL-Raga, GerardKohler, CristianoRadiske, AndressaLima, Ramón H.Rosen, Mark D.Muñoz, Francisco J.Cammarota, Martín Pablo2017-05-31T17:23:20Z2017-05-31T17:23:20Z2013https://repositorio.ufrn.br/jspui/handle/123456789/2329510.1002/hipo.22113engeIF2amemoryhippocampusNOHRI kinaseBACE1ATF4Sal003N-(2,6-dimethylbenzyl)-6,7-dimethoxy-2H-[1]benzofuro [3,2-c]pyrazol-3-amine hydrochlorideConsolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampusinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleLocal control of protein synthesis at synapses is crucial for synaptic plasticity and memory formation. However, little is known about the signals coupling neurotransmitter release with the translational machinery during these processes. Here, we studied the involvement of heme-regulated inhibitor (HRI) kinase, a kinase activated by nitric oxide that phosphorylates eukaryotic initiation factor 2α (eIF2α), in object recognition (OR) memory consolidation. Phosphorylated eIF2α mediates two opposing effects upon translation: translational arrest of most mRNAs and translational activation of selected mRNAs bearing specific features in their 5'untranslated regions (5'UTRs). We found that HRI kinase activation in the CA1 region of the dorsal hippocampus is necessary for retention of OR memory in rats. Accordingly, learning induced a transient increase in the phosphorylation state of eIF2α in dorsal CA1 which was abolished by the HRI kinase inhibitor N-(2,6-dimethylbenzyl)-6,7-dimethoxy-2H-[1]benzofuro[3,2-c]pyrazol-3-amine hydrochloride (AMI). The increase in p-eIF2α was associated with increased expression of BACE1 and activating transcription factor 4, two proteins containing eIF2α-responsive 5'UTRs in their mRNAs that play a key role in synaptic plasticity. Our data suggests that learning promotes the transient phosphorylation of eIF2α to allow for translation of specific 5'UTR-mRNAs through a process requiring HRI kinase activation.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.ufrn.br/bitstream/123456789/23295/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52TEXTConsolidation of object recognition memory requires HRI kinase-dependent phosphorylation of eIF2α in the hippocampus.pdf.txtConsolidation of object recognition memory requires HRI kinase-dependent phosphorylation of eIF2α in the hippocampus.pdf.txtExtracted texttext/plain32585https://repositorio.ufrn.br/bitstream/123456789/23295/5/Consolidation%20of%20object%20recognition%20memory%20requires%20HRI%20kinase-dependent%20phosphorylation%20of%20eIF2%ce%b1%20in%20the%20hippocampus.pdf.txt35d6d40b22e68801845c1ae1ecd4b52aMD55THUMBNAILConsolidation of object recognition memory requires HRI kinase-dependent phosphorylation of eIF2α in the hippocampus.pdf.jpgConsolidation of object recognition memory requires HRI kinase-dependent phosphorylation of eIF2α in the hippocampus.pdf.jpgIM Thumbnailimage/jpeg9494https://repositorio.ufrn.br/bitstream/123456789/23295/6/Consolidation%20of%20object%20recognition%20memory%20requires%20HRI%20kinase-dependent%20phosphorylation%20of%20eIF2%ce%b1%20in%20the%20hippocampus.pdf.jpg044a1802b6bb8303273ab573b7c02859MD56123456789/232952022-10-17 20:45:13.461oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2022-10-17T23:45:13Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.pt_BR.fl_str_mv Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
title Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
spellingShingle Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
ILL-Raga, Gerard
eIF2a
memory
hippocampus
NO
HRI kinase
BACE1
ATF4
Sal003
N-(2,6-dimethylbenzyl)-6,7-dimethoxy-2H-[1]benzofuro [3,2-c]pyrazol-3-amine hydrochloride
title_short Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
title_full Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
title_fullStr Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
title_full_unstemmed Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
title_sort Consolidation of Object Recognition Memory Requires HRI Kinase-Dependent Phosphorylation of eIF2a in the Hippocampus
author ILL-Raga, Gerard
author_facet ILL-Raga, Gerard
Kohler, Cristiano
Radiske, Andressa
Lima, Ramón H.
Rosen, Mark D.
Muñoz, Francisco J.
Cammarota, Martín Pablo
author_role author
author2 Kohler, Cristiano
Radiske, Andressa
Lima, Ramón H.
Rosen, Mark D.
Muñoz, Francisco J.
Cammarota, Martín Pablo
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv ILL-Raga, Gerard
Kohler, Cristiano
Radiske, Andressa
Lima, Ramón H.
Rosen, Mark D.
Muñoz, Francisco J.
Cammarota, Martín Pablo
dc.subject.por.fl_str_mv eIF2a
memory
hippocampus
NO
HRI kinase
BACE1
ATF4
Sal003
N-(2,6-dimethylbenzyl)-6,7-dimethoxy-2H-[1]benzofuro [3,2-c]pyrazol-3-amine hydrochloride
topic eIF2a
memory
hippocampus
NO
HRI kinase
BACE1
ATF4
Sal003
N-(2,6-dimethylbenzyl)-6,7-dimethoxy-2H-[1]benzofuro [3,2-c]pyrazol-3-amine hydrochloride
description Local control of protein synthesis at synapses is crucial for synaptic plasticity and memory formation. However, little is known about the signals coupling neurotransmitter release with the translational machinery during these processes. Here, we studied the involvement of heme-regulated inhibitor (HRI) kinase, a kinase activated by nitric oxide that phosphorylates eukaryotic initiation factor 2α (eIF2α), in object recognition (OR) memory consolidation. Phosphorylated eIF2α mediates two opposing effects upon translation: translational arrest of most mRNAs and translational activation of selected mRNAs bearing specific features in their 5'untranslated regions (5'UTRs). We found that HRI kinase activation in the CA1 region of the dorsal hippocampus is necessary for retention of OR memory in rats. Accordingly, learning induced a transient increase in the phosphorylation state of eIF2α in dorsal CA1 which was abolished by the HRI kinase inhibitor N-(2,6-dimethylbenzyl)-6,7-dimethoxy-2H-[1]benzofuro[3,2-c]pyrazol-3-amine hydrochloride (AMI). The increase in p-eIF2α was associated with increased expression of BACE1 and activating transcription factor 4, two proteins containing eIF2α-responsive 5'UTRs in their mRNAs that play a key role in synaptic plasticity. Our data suggests that learning promotes the transient phosphorylation of eIF2α to allow for translation of specific 5'UTR-mRNAs through a process requiring HRI kinase activation.
publishDate 2013
dc.date.issued.fl_str_mv 2013
dc.date.accessioned.fl_str_mv 2017-05-31T17:23:20Z
dc.date.available.fl_str_mv 2017-05-31T17:23:20Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/23295
dc.identifier.doi.none.fl_str_mv 10.1002/hipo.22113
url https://repositorio.ufrn.br/jspui/handle/123456789/23295
identifier_str_mv 10.1002/hipo.22113
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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