Recognition memory reconsolidation requires hippocampal Zif268
Open accessAbstract
Object recognition memory (ORM) serves to distinguish familiar items from novel ones. Reconsolidation is the process by which active memories are updated. The hippocampus is engaged in ORM reconsolidation through a mechanism involving induction of long-term potentiation (LTP). The transcription factor Zif268 is essential for hippocampal LTP maintenance and has been frequently associated with memory processes. However, its possible involvement in ORM reconsolidation has not been determined conclusively. Using Zif268 antisense oligonucleotides in combination with behavioural, biochemical and electrophysiological tools in rats, we found that hippocampal Zif268 is necessary to update ORM through reconsolidation but not to retrieve it or keep it stored. Our results also suggest that knocking down hippocampal Zif268 during ORM reconsolidation deletes the active recognition memory trace.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
SGK1 increases neuronal plasticity by modulating SRF and CREB1, allowing transition of stored information from short-term to long-term memories.
“Specifically, SGK1 increases neuronal plasticity by modulating the activity of transcription factors SRF and CREB1. This process allows transitioning stored information from short-term memories to long-term memories”
From Serum/glucocorticoid regulated kinase 1 (SGK1) in neurological disorders: pain or gain (2024) · cites this paper as Gonzalez et al., 2019
The Introduction (page not available) discusses Zif268 and object-recognition memory reconsolidation, not SGK1. Searches for SGK1, SRF, CREB1, and short-term-to-long-term memory transition found no passage in our copy addressing the attributed mechanism. (LLM, conf=0.76)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Behavioral and Neural Analysis of Extinction
Myers, K. M., & Davis, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)01064-4 · Cited by 918 · see citing works
Independent cellular processes for hippocampal memory consolidation and reconsolidation
Lee, J. L. C., Everitt, B. J., & Thomas, K. L. (2004) · Science · doi:10.1126/science.1095760 · Cited by 825 · see citing works
Protein Synthesis Subserves Reconsolidation or Extinction Depending on Reminder Duration
Pedreira, M. E., & Maldonado, H. (2003) · Neuron · doi:10.1016/s0896-6273(03)00352-0 · Cited by 406 · see citing works
Dunsmoor, J. E., Niv, Y., Daw, N., & Phelps, E. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.028 · Cited by 329 · see citing works
The rodent hippocampus is essential for nonspatial object memory
Cohen, S. J., Munchow, A. H., Rios, L. M., Zhang, G., Ásgeirsdóttir, H. N., & Stackman, R. W. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.002 · Cited by 325 · see citing works
Merlo, E., Milton, A. L., Goozée, Z. Y., Theobald, D. E., & Everitt, B. J. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4001-13.2014 · Cited by 242 · see citing works
DeVito, L. M., & Eichenbaum, H. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.09.014 · Cited by 164 · see citing works
Tuscher, J. J., Taxier, L. R., Fortress, A. M., & Frick, K. M. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.11.002 · Cited by 88 · see citing works
β-Arrestin–biased signaling mediates memory reconsolidation
Liu, X., Ma, L., Li, H. H., Huang, B., Li, Y. X., Tao, Y. Z., & Ma, L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421758112 · Cited by 69 · see citing works
Flagged first, then by citations
Research works printed but not linked: 44
- [2]Hammond RS Tull LE Stackman R Jr. On the delay-dependent involvement of the hippocampus in object recognition memory Neurobiol. Learn. Mem. 2004 82 26 34 10.1016/j.nlm.2004.03.005 15183168 · DOI · Paper page
- [4]Winters BD Saksida L Bussey T Object recognition memory: Neurobiological mechanisms of encoding, consolidation and retrieval Neurosci. & Biobehav. Rev. 2008 32 1055 70 10.1016/j.neubiorev.2008.04.004 18499253 · DOI
- [6]Brown MW Barker GR Aggleton JP Warburton EC What pharmacological interventions indicate concerning the role of the perirhinal cortex in recognition memory Neuropsychologia. 2012 50 3122 40 10.1016/j.neuropsychologia.2012.07.034 22841990 PMC3500694 · DOI
- [7]Rossato J On the role of hippocampal protein synthesis in the consolidation and reconsolidation of object recognition memory Learn. Mem. 2007 14 36 46 10.1101/lm.422607 17272651 PMC1838544 · DOI · Paper page
- [8]Radiske A BDNF controls object recognition memory reconsolidation Neurobiol. Learn. Mem. 2017 142 79 84 10.1016/j.nlm.2017.02.018 28274823 · DOI
- [9]Clarke JR Cammarota M Gruart A Izquierdo I Delgado-García JM Plastic modifications induced by object recognition memory processing Proc. Natl. Acad. Sci. USA 2010 107 2652 7 10.1073/pnas.0915059107 20133798 PMC2823877 · DOI · Paper page
- [10]Rossato JI PKMζ inhibition disrupts reconsolidation and erases object recognition memory J. Neurosci. 2019 39 1828 1841 10.1523/JNEUROSCI.2270-18.2018 30622166 PMC6407297 · DOI
- [11]Li L Carter J Gao X Whitehead J Tourtellotte WG The neuroplasticity-associated Arc gene is a direct transcriptional target of early growth response (Egr) transcription factors Mol. Cell. Biol. 2005 25 10286 10300 10.1128/MCB.25.23.10286-10300.2005 16287845 PMC1291244 · DOI · Paper page
- [12]Worley PF Constitutive expression of zif268 in neocortex is regulated by synaptic activity Proc. Natl. Acad. Sci. USA 1991 88 5106 10 10.1073/pnas.88.12.5106 1828891 PMC51820 · DOI
- [13]Kaczmarek L Chaudhurib A Sensory regulation of immediate–early gene expression in mammalian visual cortex: implications for functional mapping and neural plasticity Brain Research Rev. 1997 23 237 256 10.1016/S0165-0173(97)00005-2 9164673 · DOI
- [14]Davis S Bozon B Laroche S How necessary is the activation of the immediate early gene zif268 in synaptic plasticity and learning? Behav. Brain Res. 2003 142 17 30 10.1016/S0166-4328(02)00421-7 12798262 · DOI
- [15]Granado N D1 but not D5 dopamine receptors are critical for LTP, spatial learning, and LTP-Induced arc and zif268 expression in the hippocampus Cereb. Cortex. 2008 18 1 12 10.1093/cercor/bhm026 17395606 · DOI
- [16]Neves G Cooke SF Bliss TVP Synaptic plasticity, memory and the hippocampus: a neural network approach to causality Nat. Rev. Neurosci. 2008 9 65 75 10.1038/nrn2303 18094707 · DOI
- [17]Renaudineau S Poucet B Laroche S Davis S Save E Impaired long-term stability of CA1 place cell representation in mice lacking the transcription factor zif268/egr1 Proc. Natl. Acad. Sci. USA 2009 106 11771 5 10.1073/pnas.0900484106 19556537 PMC2710630 · DOI
- [18]Bozon B Davis S Laroche S Regulated transcription of the immediate‐early gene Zif268: Mechanisms and gene dosage‐dependent function in synaptic plasticity and memory formation Hippocampus. 2002 12 570 577 10.1002/hipo.10100 12440572 · DOI
- [19]Lonergan ME Gafford GM Jarome TJ Helmstetter FJ Time-dependent expression of Arc and Zif268 after acquisition of fear conditioning Neural Plasticity. 2010 2010 139891 10.1155/2010/139891 20592749 PMC2877205 · DOI
- [20]Penke Z Zif268/Egr1 gain of function facilitates hippocampal synaptic plasticity and long-term spatial recognition memory Philos. Trans. R. Soc. Lond. B. Biol. Sci. 2014 369 20130159 10.1098/rstb.2013.0159 24298160 PMC3843890 · DOI
- [21]Jones ML A requirement for the immediate early gene Zif268 in the expression of late LTP and long-term memories Nat. Neurosci. 2001 4 289 296 10.1038/85138 11224546 · DOI
- [23]von Hertzen LSJ Giese KP Memory reconsolidation engages only a subset of immediate-early genes induced during consolidation J. Neurosci. 2005 25 1935 1942 10.1523/JNEUROSCI.4707-04.2005 15728833 PMC6726052 · DOI
- [24]Lee JL Hynds RE Divergent cellular pathways of hippocampal memory consolidation and reconsolidation Hippocampus. 2013 23 233 44 10.1002/hipo.22083 23197404 PMC3675315 · DOI
- [25]Trent S Barnes P Hall J Thomas KL Rescue of long-term memory after reconsolidation blockade Nat. Commun. 2015 6 7897 10.1038/ncomms8897 26238574 PMC4532853 · DOI
- [26]Lee JL Di Ciano P Thomas KL Everitt BJ Disrupting reconsolidation Report of drug memories reduces cocaine-seeking behavior Neuron. 2005 47 795 801 10.1016/j.neuron.2005.08.007 16157275 · DOI
- [27]Morici JF 5-HT2a receptor in mPFC influences context-guided reconsolidation of object memory in perirhinal cortex Elife. 2018 7 e33746 10.7554/eLife.33746 29717980 PMC5931799 · DOI
- [30]Suzuki A Memory reconsolidation and extinction have distinct temporal and biochemical signatures J. Neurosci. 2004 24 4787 4795 10.1523/JNEUROSCI.5491-03.2004 15152039 PMC6729467 · DOI · Paper page
- [32]Lima RH Infusion of protein synthesis inhibitors in the entorhinal cortex blocks consolidation but not reconsolidation of object recognition memory Neurobiol. Learn. Mem. 2009 91 466 722 10.1016/j.nlm.2008.12.009 19141326 · DOI · Paper page
- [33]Kelly A Laroche S Davis S Activation of mitogen-activated protein kinase/extracellular signal-regulated kinase in hippocampal circuitry is required for consolidation and reconsolidation of recognition memory J. Neurosci. 2003 23 5354 60 10.1523/JNEUROSCI.23-12-05354.2003 12832561 PMC6741214 · DOI
- [34]Akirav I Maroun M Ventromedial prefrontal cortex is obligatory for consolidation and reconsolidation of object recognition memory Cereb. Cortex. 2006 16 1759 65 10.1093/cercor/bhj114 16421330 · DOI
- [35]Balderas I Rodriguez-Ortiz CJ Bermudez-Rattoni F Retrieval and reconsolidation of object recognition memory are independent processes in the perirhinal cortex Neurosci. 2013 253 398 405 10.1016/j.neuroscience.2013.09.001 24042035 · DOI
- [37]Rossato JI State-dependent effect of dopamine D1/D5 receptors inactivation on memory destabilization and reconsolidation Behav Brain Res. 2015 285 194 9 10.1016/j.bbr.2014.09.009 25219363 · DOI · Paper page
- [38]Nyberg L Any novelty in hippocampal formation and memory? Curr Opin Neurol. 2005 18 424 8 10.1097/01.wco.0000168080.99730.1c 16003119 · DOI
- [39]van Kesteren MT Ruiter DJ Fernández G Henson RN How schema and novelty augment memory formation Trends Neurosci. 2012 35 211 9 10.1016/j.tins.2012.02.001 22398180 · DOI · Paper page
- [40]Duszkiewicz AJ McNamara CG Takeuchi T Genzel L Novelty and Dopaminergic Modulation of Memory Persistence: A Tale of Two Systems Trends Neurosci. 2019 42 102 14 10.1016/j.tins.2018.10.002 30455050 PMC6352318 · DOI
- [41]Rodriguez-Ortiz CJ Intrahippocampal anisomycin infusions disrupt previously consolidated spatial memory only when memory is updated Neurobiol. Learn. Mem. 2008 89 352 359 10.1016/j.nlm.2007.10.004 18054256 · DOI
- [42]Winters BD Tucci MC Jacklin DL Reid JM Newsome J On the dynamic nature of the engram: evidence for circuit-level reorganization of object memory traces following reactivation J. Neurosci. 2011 31 17719 28 10.1523/JNEUROSCI.2968-11.2011 22131432 PMC6623795 · DOI
- [43]Whitesell L Stability, clearance, and disposition of intraventricularly administered oligodeoxynucleotides: implications for therapeutic application within the central nervous system Proc. Natl. Acad. Sci. USA 1993 90 4665 9 10.1073/pnas.90.10.4665 8506315 PMC46573 · DOI
- [44]Morris M Lucion AB Antisense oligonucleotides in the study of neuroendocrine systems J. Neuroendocrinol. 1995 7 493 500 10.1111/j.1365-2826.1995.tb00787.x 7496391 · DOI
- [45]Culman J Antisense oligonucleotides in the study of central mechanisms of the cardiovascular regulation Exp. Physiol. 2000 85 757 67 10.1111/j.1469-445X.2000.02143.x 11187969 · DOI
- [46]Abraham WC Logan B Thompson VL Williams JM Tate WP Sequence-independent effects of phosphorothiolated oligonucleotides on synaptic transmission and excitability in the hippocampus in vivo Neuropharmacology. 1997 36 345 52 10.1016/S0028-3908(97)00013-0 9175613 · DOI
- [47]Lee JLC Nader K Schiller D An update on memory reconsolidation updating Trends. Cogn. Sci. 2017 21 531 545 10.1016/j.tics.2017.04.006 28495311 PMC5605913 · DOI · Paper page
- [48]Clem RL Schiller D New Learning and Unlearning: Strangers or Accomplices in Threat Memory Attenuation? Trends Neurosci. 2016 39 340 351 10.1016/j.tins.2016.03.003 27079843 PMC4972342 · DOI · Paper page
- [50]Myers KM Davis M Mechanisms of fear extinction Mol. Psychiatry. 2007 12 120 150 10.1038/sj.mp.4001939 17160066 · DOI · Paper page
- [52]Ennaceur A Delacour J A new one-trial test for neurobiological studies of memory in rats 1: Behavioral data Behav. Brain. Res. 1988 31 47 59 10.1016/0166-4328(88)90157-X 3228475 · DOI · Paper page
- [53]Rossato JI Bevilaqua LR Medina JH Izquierdo I Cammarota M Retrieval induces hippocampal-dependent reconsolidation of spatial memory Learn. Mem. 2006 13 431 40 10.1101/lm.315206 16882860 PMC1538920 · DOI
- [54]Radiske A Prior learning of relevant nonaversive information is a boundary condition for avoidance memory reconsolidation in the rat hippocampus J. Neurosci. 2017 37 9675 9685 10.1523/JNEUROSCI.1372-17.2017 28887385 PMC6596618 · DOI
Cited by
Sorted by citations
Serum/glucocorticoid regulated kinase 1 (SGK1) in neurological disorders: pain or gain
Howard, P. G., Zou, P., Zhang, Y., Huang, F., Tesic, V., Wu, C. Y.-C., & Lee, R. H.-C. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114973 · Cited by 13 · see citing works
- Authors
- Gonzalez, M. C., Rossato, J. I., Radiske, A., Pádua Reis, M., & Cammarota, M.
- Affiliations
- Universidade Federal do Rio Grande do Norte (BR)
- Venue
- Scientific Reports
- Published
- 2019-11-12
- Volume
- 9
- Issue
- 1
- Pages
- 16620-16620
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC6851087
- OpenAlex
- W2984078984
- Cited by
- 35
- References
- 9
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 7 · 2023: 4 · 2022: 9 · 2021: 3 · 2019: 1
- FWCI
- 1.89
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (publishedVersion, other-oa)
- Americanae (AECID Library) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, other-oa)
- Funders
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Universidade Federal do Rio Grande do Norte
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- object recognition memory, memory reconsolidation, Zif268, hippocampus, long-term potentiation, transcription factors, antisense oligonucleotides, memory updating, memory retrieval, memory traces
- MeSH terms
- Memory Consolidation, Animals, Fluorescent Antibody Technique, Hippocampus, Male, Rats, Wistar, Maze Learning, Recognition, Psychology, Rats, Early Growth Response Protein 1, Gene Knockdown Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review