Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

The molecular and cellular biology of enhanced cognition

Key Points

  • Although there is considerable evidence for animals and people with cognitive enhancements, mechanistic studies of enhanced cognition are comparatively rare.

  • Genetic manipulations of more than 30 different genes have been shown to enhance learning and memory (L&M) in mutant mice. These 'smart' mice provide powerful tools to investigate the cellular and molecular mechanisms underlying L&M enhancements.

  • Strikingly, long-term potentiation (LTP) is enhanced in most of the mutant mice with enhanced L&M, providing a compelling argument for a role of LTP-like mechanisms in L&M.

  • It is possible to enhance synaptic plasticity and L&M by manipulating various neuronal signalling molecules, ranging from membrane receptors to nuclear transcription factors. Interestingly, N-methyl-D-aspartate (NMDA) receptor signalling and subsequent cyclic-AMP response-element-binding protein (CREB)-dependent transcription are upregulated in many mutant mice with enhanced L&M.

  • Targeting the molecular mechanisms that are associated with L&M enhancements may lead to the development of general therapies for cognitive disorders, and could represent a novel strategy to address the extraordinary complexity of the genetic and environmental factors responsible for the myriad of cognitive disorders that affect a surprisingly large percentage of the population.

Abstract

Most molecular and cellular studies of cognitive function have focused on either normal or pathological states, but recent research with transgenic mice has started to address the mechanisms of enhanced cognition. These results point to key synaptic and nuclear signalling events that can be manipulated to facilitate the induction or increase the stability of synaptic plasticity, and therefore enhance the acquisition or retention of information. Here, we review these surprising findings and explore their implications to both mechanisms of learning and memory and to ongoing efforts to develop treatments for cognitive disorders. These findings represent the beginning of a fundamental new approach in the study of enhanced cognition.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: NMDAR-dependent signalling and downstream kinases and phosphatases implicated in learning and memory enhancement.
Figure 2: Regulation of CREB-dependent gene expression involved in memory formation.
Figure 3: Integrating pathways for learning and memory enhancement.

Similar content being viewed by others

References

  1. Selkoe, D. J. Alzheimer's disease: genes, proteins, and therapy. Physiol. Rev. 81, 741–766 (2001).

    CAS  PubMed  Google Scholar 

  2. Li, W. et al. Specific developmental disruption of disrupted-in-schizophrenia-1 function results in schizophrenia-related phenotypes in mice. Proc. Natl Acad. Sci. USA 104, 18280–18285 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Harwood, A. J. & Agam, G. Search for a common mechanism of mood stabilizers. Biochem. Pharmacol. 66, 179–189 (2003).

    CAS  PubMed  Google Scholar 

  4. Thomas, B. & Beal, M. F. Parkinson's disease. Hum. Mol. Genet. 16 (Suppl. 2), 183–194 (2007).

    Google Scholar 

  5. Costa, R. M. & Silva, A. J. Molecular and cellular mechanisms underlying the cognitive deficits associated with neurofibromatosis 1. J. Child. Neurol. 17, 622–626; discussion 627–629, 646–651 (2002).

    PubMed  Google Scholar 

  6. Rosenzweig, E. S. & Barnes, C. A. Impact of aging on hippocampal function: plasticity, network dynamics, and cognition. Prog. Neurobiol. 69, 143–179 (2003).

    CAS  PubMed  Google Scholar 

  7. Ehninger, D. et al. Reversal of learning deficits in a Tsc2(±) mouse model of tuberous sclerosis. Nature Med. (2008).

  8. Luria, A. R. The mind of a mnemonist; a little book about a vast memory (Basic Books, New York,1968).

    Google Scholar 

  9. Tang, Y. P. et al. Genetic enhancement of learning and memory in mice. Nature 401, 63–69 (1999). This paper describes the 'doogie' mice, which overexpress NR2B in the adult forebrain. Although this was not the first published paper reporting mice with LTP and learning and memory enhancements, the study triggered a great deal of interest in the media.

    CAS  PubMed  Google Scholar 

  10. Kiyama, Y. et al. Increased thresholds for long-term potentiation and contextual learning in mice lacking the NMDA-type glutamate receptor epsilon1 subunit. J. Neurosci. 18, 6704–6712 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  11. McHugh, T. J. et al. Dentate gyrus NMDA receptors mediate rapid pattern separation in the hippocampal network. Science 317, 94–99 (2007).

    CAS  PubMed  Google Scholar 

  12. Morris, R. G., Anderson, E., Lynch, G. S. & Baudry, M. Selective impairment of learning and blockade of long-term potentiation by an N-methyl-D-aspartate receptor antagonist, AP5. Nature 319, 774–776 (1986). A classic paper that used a pharmacological manipulation to demonstrate the crucial role of NMDA receptors in spatial learning.

    CAS  PubMed  Google Scholar 

  13. Nakazawa, K. et al. Requirement for hippocampal CA3 NMDA receptors in associative memory recall. Science 297, 211–218 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Nakazawa, K. et al. Hippocampal CA3 NMDA receptors are crucial for memory acquisition of one-time experience. Neuron 38, 305–315 (2003).

    CAS  PubMed  Google Scholar 

  15. Sakimura, K. et al. Reduced hippocampal LTP and spatial learning in mice lacking NMDA receptor epsilon 1 subunit. Nature 373, 151–155 (1995).

    CAS  PubMed  Google Scholar 

  16. Tsien, J. Z., Huerta, P. T. & Tonegawa, S. The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory. Cell 87, 1327–1338 (1996).

    CAS  PubMed  Google Scholar 

  17. Matynia, A., Kushner, S. A. & Silva, A. J. Genetic approaches to molecular and cellular cognition: a focus on LTP and learning and memory. Annu. Rev. Genet. 36, 687–720 (2002).

    CAS  PubMed  Google Scholar 

  18. Bliss, T. V. & Collingridge, G. L. A synaptic model of memory: long-term potentiation in the hippocampus. Nature 361, 31–39 (1993).

    CAS  PubMed  Google Scholar 

  19. Monyer, H., Burnashev, N., Laurie, D. J., Sakmann, B. & Seeburg, P. H. Developmental and regional expression in the rat brain and functional properties of four NMDA receptors. Neuron 12, 529–540 (1994).

    CAS  PubMed  Google Scholar 

  20. Sheng, M., Cummings, J., Roldan, L. A., Jan, Y. N. & Jan, L. Y. Changing subunit composition of heteromeric NMDA receptors during development of rat cortex. Nature 368, 144–147 (1994).

    CAS  PubMed  Google Scholar 

  21. Manabe, T. et al. Facilitation of long-term potentiation and memory in mice lacking nociceptin receptors. Nature 394, 577–581 (1998).

    CAS  PubMed  Google Scholar 

  22. Harris, K. M. & Teyler, T. J. Developmental onset of long-term potentiation in area CA1 of the rat hippocampus. J. Physiol. 346, 27–48 (1984).

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Morris, R. G., Garrud, P., Rawlins, J. N. & O'Keefe, J. Place navigation impaired in rats with hippocampal lesions. Nature 297, 681–683 (1982).

    CAS  PubMed  Google Scholar 

  24. Walker, D. L. & Davis, M. The role of amygdala glutamate receptors in fear learning, fear-potentiated startle, and extinction. Pharmacol. Biochem. Behav. 71, 379–392 (2002).

    CAS  PubMed  Google Scholar 

  25. Cao, X. et al. Maintenance of superior learning and memory function in NR2B transgenic mice during ageing. Eur. J. Neurosci. 25, 1815–1822 (2007).

    PubMed  Google Scholar 

  26. Jeon, D. et al. Ablation of Ca2+ channel beta3 subunit leads to enhanced N-methyl-D-aspartate receptor-dependent long term potentiation and improved long term memory. J. Biol. Chem. 283, 12093–12101 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  27. Malinow, R. & Malenka, R. C. AMPA receptor trafficking and synaptic plasticity. Annu. Rev. Neurosci. 25, 103–126 (2002).

    CAS  PubMed  Google Scholar 

  28. Rumpel, S., LeDoux, J., Zador, A. & Malinow, R. Postsynaptic receptor trafficking underlying a form of associative learning. Science 308, 83–88 (2005).

    CAS  PubMed  Google Scholar 

  29. Wong, R. W., Setou, M., Teng, J., Takei, Y. & Hirokawa, N. Overexpression of motor protein KIF17 enhances spatial and working memory in transgenic mice. Proc. Natl Acad. Sci. USA 99, 14500–14505 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  30. Guillaud, L., Setou, M. & Hirokawa, N. KIF17 dynamics and regulation of NR2B trafficking in hippocampal neurons. J. Neurosci. 23, 131–140 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Gonzalez, G. A. & Montminy, M. R. Cyclic AMP stimulates somatostatin gene transcription by phosphorylation of CREB at serine 133. Cell 59, 675–680 (1989).

    CAS  PubMed  Google Scholar 

  32. Bourtchuladze, R. et al. Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein. Cell 79, 59–68 (1994). This study showed that both the stability of synaptic plasticity (LTP) and long-term memory are impaired in CREB-knockout mice, highlighting the key role of CREB in memory in the mammalian brain.

    CAS  PubMed  Google Scholar 

  33. Kida, S. et al. CREB required for the stability of new and reactivated fear memories. Nature Neurosci. 5, 348–355 (2002). This study used an inducible transgenic technique, involving the ligand-binding domain of the oestrogen receptor (LBD)-fusion protein, to study the in vivo role of CREB in memory consolidation and reconsolidation.

    CAS  PubMed  Google Scholar 

  34. West, A. E. et al. Calcium regulation of neuronal gene expression. Proc. Natl Acad. Sci. USA 98, 11024–11031 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  35. Dong, Y. N., Wu, H. Y., Hsu, F. C., Coulter, D. A. & Lynch, D. R. Developmental and cell-selective variations in N-methyl-D-aspartate receptor degradation by calpain. J. Neurochem. 99, 206–217 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Simpkins, K. L. et al. Selective activation induced cleavage of the NR2B subunit by calpain. J. Neurosci. 23, 11322–11331 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  37. Husi, H., Ward, M. A., Choudhary, J. S., Blackstock, W. P. & Grant, S. G. Proteomic analysis of NMDA receptor-adhesion protein signaling complexes. Nature Neurosci. 3, 661–669 (2000).

    CAS  PubMed  Google Scholar 

  38. Hawasli, A. H. et al. Cyclin-dependent kinase 5 governs learning and synaptic plasticity via control of NMDAR degradation. Nature Neurosci. 10, 880–886 (2007).

    CAS  PubMed  Google Scholar 

  39. Angelo, M., Plattner, F. & Giese, K. P. Cyclin-dependent kinase 5 in synaptic plasticity, learning and memory. J. Neurochem. 99, 353–370 (2006).

    CAS  PubMed  Google Scholar 

  40. Hawasli, A. H. & Bibb, J. A. Alternative roles for Cdk5 in learning and synaptic plasticity. Biotechnol. J. 2, 941–948 (2007).

    CAS  PubMed  Google Scholar 

  41. Fischer, A., Sananbenesi, F., Pang, P. T., Lu, B. & Tsai, L. H. Opposing roles of transient and prolonged expression of p25 in synaptic plasticity and hippocampus-dependent memory. Neuron 48, 825–838 (2005).

    CAS  PubMed  Google Scholar 

  42. Mamiya, T. et al. Neuronal mechanism of nociceptin-induced modulation of learning and memory: involvement of N-methyl-D-aspartate receptors. Mol. Psychiatry 8, 752–765 (2003).

    CAS  PubMed  Google Scholar 

  43. Noda, Y. et al. Role of nociceptin systems in learning and memory. Peptides 21, 1063–1069 (2000).

    CAS  PubMed  Google Scholar 

  44. Lynch, G. Memory enhancement: the search for mechanism-based drugs. Nature Neurosci. 5, S1035–S1038 (2002).

    Google Scholar 

  45. Shanley, L. J., Irving, A. J. & Harvey, J. Leptin enhances NMDA receptor function and modulates hippocampal synaptic plasticity. J. Neurosci. 21, RC186 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  46. Oomura, Y. et al. Leptin facilitates learning and memory performance and enhances hippocampal CA1 long-term potentiation and CaMK II phosphorylation in rats. Peptides 27, 2738–2749 (2006).

    CAS  PubMed  Google Scholar 

  47. Lisman, J., Schulman, H. & Cline, H. The molecular basis of CaMKII function in synaptic and behavioural memory. Nature Rev. Neurosci. 3, 175–190 (2002). An excellent review of the role of αCaMKII in synaptic plasticity and learning and memory.

    CAS  Google Scholar 

  48. Mulkey, R. M. & Malenka, R. C. Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus. Neuron 9, 967–975 (1992).

    CAS  PubMed  Google Scholar 

  49. Grover, L. M. & Teyler, T. J. Two components of long-term potentiation induced by different patterns of afferent activation. Nature 347, 477–479 (1990).

    CAS  PubMed  Google Scholar 

  50. Balschun, D. et al. Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning. Embo J. 18, 5264–5273 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  51. Frankel, W. N. Mouse strain backgrounds: more than black and white. Neuron 20, 183 (1998).

    CAS  PubMed  Google Scholar 

  52. Blaustein, M. P. & Lederer, W. J. Sodium/calcium exchange: its physiological implications. Physiol. Rev. 79, 763–854 (1999).

    CAS  PubMed  Google Scholar 

  53. Jeon, D. et al. Enhanced learning and memory in mice lacking Na+/Ca2+ exchanger 2. Neuron 38, 965–976 (2003).

    CAS  PubMed  Google Scholar 

  54. Bear, M. F. & Malenka, R. C. Synaptic plasticity: LTP and LTD. Curr. Opin. Neurobiol. 4, 389–399 (1994). An introductory review to the mechanism of two key forms of synaptic plasticity: LTP and LTD.

    CAS  PubMed  Google Scholar 

  55. Soderling, T. R. & Derkach, V. A. Postsynaptic protein phosphorylation and LTP. Trends Neurosci. 23, 75–80 (2000).

    CAS  PubMed  Google Scholar 

  56. Blitzer, R. D., Wong, T., Nouranifar, R., Iyengar, R. & Landau, E. M. Postsynaptic cAMP pathway gates early LTP in hippocampal CA1 region. Neuron 15, 1403–1414 (1995).

    CAS  PubMed  Google Scholar 

  57. Abel, T., Martin, K. C., Bartsch, D. & Kandel, E. R. Memory suppressor genes: inhibitory constraints on the storage of long-term memory. Science 279, 338–341 (1998). This article reviews the role of negative regulators such as the transcriptional repressor CREB2 in synaptic plasticity and memory, with an emphasis on the removal of these constraints in memory storage.

    CAS  PubMed  Google Scholar 

  58. Pastalkova, E. et al. Storage of spatial information by the maintenance mechanism of LTP. Science 313, 1141–1144 (2006).

    CAS  PubMed  Google Scholar 

  59. Silva, A. J., Paylor, R., Wehner, J. M. & Tonegawa, S. Impaired spatial learning in alpha-calcium-calmodulin kinase II mutant mice. Science 257, 206–211 (1992). The first paper demonstrating the use of genetic manipulations in the study of mechanisms of cognitive function in mammals.

    CAS  PubMed  Google Scholar 

  60. Silva, A. J., Stevens, C. F., Tonegawa, S. & Wang, Y. Deficient hippocampal long-term potentiation in alpha-calcium-calmodulin kinase II mutant mice. Science 257, 201–206 (1992).

    CAS  PubMed  Google Scholar 

  61. Sweatt, J. D. Mitogen-activated protein kinases in synaptic plasticity and memory. Curr. Opin. Neurobiol. 14, 311–317 (2004).

    CAS  PubMed  Google Scholar 

  62. Mansuy, I. M., Mayford, M., Jacob, B., Kandel, E. R. & Bach, M. E. Restricted and regulated overexpression reveals calcineurin as a key component in the transition from short-term to long-term memory. Cell 92, 39–49 (1998).

    CAS  PubMed  Google Scholar 

  63. Mansuy, I. M. et al. Inducible and reversible gene expression with the rtTA system for the study of memory. Neuron 21, 257–265 (1998).

    CAS  PubMed  Google Scholar 

  64. Genoux, D. et al. Protein phosphatase 1 is a molecular constraint on learning and memory. Nature 418, 970–975 (2002).

    CAS  PubMed  Google Scholar 

  65. Blitzer, R. D. et al. Gating of CaMKII by cAMP-regulated protein phosphatase activity during LTP. Science 280, 1940–1942 (1998).

    CAS  PubMed  Google Scholar 

  66. Shi, J., Townsend, M. & Constantine-Paton, M. Activity-dependent induction of tonic calcineurin activity mediates a rapid developmental downregulation of NMDA receptor currents. Neuron 28, 103–114 (2000).

    CAS  PubMed  Google Scholar 

  67. Liu, J. P., Sim, A. T. & Robinson, P. J. Calcineurin inhibition of dynamin I GTPase activity coupled to nerve terminal depolarization. Science 265, 970–973 (1994).

    CAS  PubMed  Google Scholar 

  68. Lisman, J. A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory. Proc. Natl Acad. Sci. USA 86, 9574–9578 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  69. Chan, G. C., Tonegawa, S. & Storm, D. R. Hippocampal neurons express a calcineurin-activated adenylyl cyclase. J. Neurosci. 25, 9913–9918 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  70. Winder, D. G., Mansuy, I. M., Osman, M., Moallem, T. M. & Kandel, E. R. Genetic and pharmacological evidence for a novel, intermediate phase of long-term potentiation suppressed by calcineurin. Cell 92, 25–37 (1998).

    CAS  PubMed  Google Scholar 

  71. Mansuy, I. M. & Shenolikar, S. Protein serine/threonine phosphatases in neuronal plasticity and disorders of learning and memory. Trends Neurosci. 29, 679–686 (2006).

    CAS  PubMed  Google Scholar 

  72. Malleret, G. et al. Inducible and reversible enhancement of learning, memory, and long-term potentiation by genetic inhibition of calcineurin. Cell 104, 675–686 (2001).

    CAS  PubMed  Google Scholar 

  73. Baumgartel, K. et al. Control of the establishment of aversive memory by calcineurin and Zif268. Nature Neurosci. 11, 572–578 (2008).

    PubMed  Google Scholar 

  74. Mansuy, I. M. Calcineurin in memory and bidirectional plasticity. Biochem. Biophys. Res. Commun. 311, 1195–1208 (2003).

    CAS  PubMed  Google Scholar 

  75. Zeng, H. et al. Forebrain-specific calcineurin knockout selectively impairs bidirectional synaptic plasticity and working/episodic-like memory. Cell 107, 617–629 (2001).

    CAS  PubMed  Google Scholar 

  76. Ikegami, S. & Inokuchi, K. Antisense DNA against calcineurin facilitates memory in contextual fear conditioning by lowering the threshold for hippocampal long-term potentiation induction. Neuroscience 98, 637–646 (2000).

    CAS  PubMed  Google Scholar 

  77. Ikegami, S. et al. A facilitatory effect on the induction of long-term potentiation in vivo by chronic administration of antisense oligodeoxynucleotides against catalytic subunits of calcineurin. Brain Res. Mol. Brain Res. 41, 183–191 (1996).

    CAS  PubMed  Google Scholar 

  78. Morishita, W. et al. Regulation of synaptic strength by protein phosphatase 1. Neuron 32, 1133–1148 (2001).

    CAS  PubMed  Google Scholar 

  79. Wong, S. T. et al. Calcium-stimulated adenylyl cyclase activity is critical for hippocampus-dependent long-term memory and late phase LTP. Neuron 23, 787–798 (1999).

    CAS  PubMed  Google Scholar 

  80. Wang, H., Ferguson, G. D., Pineda, V. V., Cundiff, P. E. & Storm, D. R. Overexpression of type-1 adenylyl cyclase in mouse forebrain enhances recognition memory and LTP. Nature Neurosci. 7, 635–642 (2004).

    CAS  PubMed  Google Scholar 

  81. Shan, Q., Chan, G. C. & Storm, D. R. Type 1 adenylyl cyclase is essential for maintenance of remote contextual fear memory. J. Neurosci. 28, 12864–12867 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  82. Isiegas, C. et al. A novel conditional genetic system reveals that increasing neuronal cAMP enhances memory and retrieval. J. Neurosci. 28, 6220–6230 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  83. Barad, M., Bourtchouladze, R., Winder, D. G., Golan, H. & Kandel, E. Rolipram, a type IV-specific phosphodiesterase inhibitor, facilitates the establishment of long-lasting long-term potentiation and improves memory. Proc. Natl Acad. Sci. USA 95, 15020–15025 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  84. Bourtchouladze, R. et al. A mouse model of Rubinstein-Taybi syndrome: defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4. Proc. Natl Acad. Sci. USA 100, 10518–10522 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  85. Alarcon, J. M. et al. Chromatin acetylation, memory, and LTP are impaired in CBP± mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration. Neuron 42, 947–959 (2004).

    CAS  PubMed  Google Scholar 

  86. Yin, J. C. et al. Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila. Cell 79, 49–58 (1994).

    CAS  PubMed  Google Scholar 

  87. Bartsch, D., Casadio, A., Karl, K. A., Serodio, P. & Kandel, E. R. CREB1 encodes a nuclear activator, a repressor, and a cytoplasmic modulator that form a regulatory unit critical for long-term facilitation. Cell 95, 211–223 (1998).

    CAS  PubMed  Google Scholar 

  88. Kandel, E. R. The molecular biology of memory storage: a dialogue between genes and synapses. Science 294, 1030–1038 (2001).

    CAS  PubMed  Google Scholar 

  89. Silva, A. J., Kogan, J. H., Frankland, P. W. & Kida, S. CREB and memory. Annu. Rev. Neurosci. 21, 127–148 (1998).

    CAS  PubMed  Google Scholar 

  90. Bozon, B. et al. MAPK, CREB and zif268 are all required for the consolidation of recognition memory. Philos. Trans. R. Soc. Lond. B Biol. Sci. 358, 805–814 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  91. Yin, J. C. & Tully, T. CREB and the formation of long-term memory. Curr. Opin. Neurobiol. 6, 264–268 (1996).

    CAS  PubMed  Google Scholar 

  92. Josselyn, S. A., Kida, S. & Silva, A. J. Inducible repression of CREB function disrupts amygdala-dependent memory. Neurobiol. Learn. Mem. 82, 159–163 (2004).

    CAS  PubMed  Google Scholar 

  93. Wu, L. J. et al. Genetic enhancement of trace fear memory and cingulate potentiation in mice overexpressing Ca2+/calmodulin-dependent protein kinase IV. Eur. J. Neurosci. 27, 1923–1932 (2008).

    PubMed  Google Scholar 

  94. Fukushima, H. et al. Upregulation of calcium/calmodulin-dependent protein kinase IV improves memory formation and rescues memory loss with aging. J. Neurosci. 28, 9910–9919 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  95. Alberini, C. M., Ghirardi, M., Metz, R. & Kandel, E. R. C/EBP is an immediate-early gene required for the consolidation of long-term facilitation in Aplysia. Cell 76, 1099–1114 (1994).

    CAS  PubMed  Google Scholar 

  96. Lee, J. A. et al. Overexpression of and RNA interference with the CCAAT enhancer-binding protein on long-term facilitation of Aplysia sensory to motor synapses. Learn. Mem. 8, 220–226 (2001).

    PubMed  PubMed Central  Google Scholar 

  97. Taubenfeld, S. M., Milekic, M. H., Monti, B. & Alberini, C. M. The consolidation of new but not reactivated memory requires hippocampal C/EBPbeta. Nature Neurosci. 4, 813–818 (2001).

    CAS  PubMed  Google Scholar 

  98. Sterneck, E. et al. Selectively enhanced contextual fear conditioning in mice lacking the transcriptional regulator CCAAT/enhancer binding protein delta. Proc. Natl Acad. Sci. USA 95, 10908–10913 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  99. Chen, A. et al. Inducible enhancement of memory storage and synaptic plasticity in transgenic mice expressing an inhibitor of ATF4 (CREB-2) and C/EBP proteins. Neuron 39, 655–669 (2003).

    CAS  PubMed  Google Scholar 

  100. Karpinski, B. A., Morle, G. D., Huggenvik, J., Uhler, M. D. & Leiden, J. M. Molecular cloning of human CREB-2: an ATF/CREB transcription factor that can negatively regulate transcription from the cAMP response element. Proc. Natl Acad. Sci. USA 89, 4820–4824 (1992).

    CAS  PubMed  PubMed Central  Google Scholar 

  101. Yin, J. C., Del Vecchio, M., Zhou, H. & Tully, T. CREB as a memory modulator: induced expression of a dCREB2 activator isoform enhances long-term memory in Drosophila. Cell 81, 107–115 (1995).

    CAS  PubMed  Google Scholar 

  102. Bartsch, D. et al. Aplysia CREB2 represses long-term facilitation: relief of repression converts transient facilitation into long-term functional and structural change. Cell 83, 979–992 (1995).

    CAS  PubMed  Google Scholar 

  103. Costa-Mattioli, M. et al. Translational control of hippocampal synaptic plasticity and memory by the eIF2alpha kinase GCN2. Nature 436, 1166–1173 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  104. Costa-Mattioli, M. et al. eIF2alpha phosphorylation bidirectionally regulates the switch from short- to long-term synaptic plasticity and memory. Cell 129, 195–206 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  105. Harding, H. P. et al. Regulated translation initiation controls stress-induced gene expression in mammalian cells. Mol. Cell 6, 1099–1108 (2000).

    CAS  PubMed  Google Scholar 

  106. Sonenberg, N. & Dever, T. E. Eukaryotic translation initiation factors and regulators. Curr. Opin. Struct. Biol. 13, 56–63 (2003).

    CAS  PubMed  Google Scholar 

  107. Hsieh, J. & Gage, F. H. Chromatin remodeling in neural development and plasticity. Curr. Opin. Cell Biol. 17, 664–671 (2005).

    CAS  PubMed  Google Scholar 

  108. Guan, Z. et al. Integration of long-term-memory-related synaptic plasticity involves bidirectional regulation of gene expression and chromatin structure. Cell 111, 483–493 (2002). This is one of the first papers to demonstrate the role of chromatin modifications in synaptic plasticity. This study showed that the expression of an immediate early gene, C/EBP, is bidirectionally regulated by a mechanism involving histone acetylation in Aplysia.

    CAS  PubMed  Google Scholar 

  109. Korzus, E., Rosenfeld, M. G. & Mayford, M. CBP histone acetyltransferase activity is a critical component of memory consolidation. Neuron 42, 961–972 (2004). One of the first reports showing the key role of epigenetic mechanisms in behavioural memory in the mammalian nervous system.

    CAS  PubMed  PubMed Central  Google Scholar 

  110. Levenson, J. M. et al. Regulation of histone acetylation during memory formation in the hippocampus. J. Biol. Chem. 279, 40545–40559 (2004).

    CAS  PubMed  Google Scholar 

  111. Yeh, S. H., Lin, C. H. & Gean, P. W. Acetylation of nuclear factor-kappaB in rat amygdala improves long-term but not short-term retention of fear memory. Mol. Pharmacol. 65, 1286–1292 (2004).

    CAS  PubMed  Google Scholar 

  112. Vecsey, C. G. et al. Histone deacetylase inhibitors enhance memory and synaptic plasticity via CREB:CBP-dependent transcriptional activation. J. Neurosci. 27, 6128–6140 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  113. Qian, Z., Gilbert, M. E., Colicos, M. A., Kandel, E. R. & Kuhl, D. Tissue-plasminogen activator is induced as an immediate-early gene during seizure, kindling and long-term potentiation. Nature 361, 453–457 (1993).

    CAS  PubMed  Google Scholar 

  114. Huang, Y. Y. et al. Mice lacking the gene encoding tissue-type plasminogen activator show a selective interference with late-phase long-term potentiation in both Schaffer collateral and mossy fiber pathways. Proc. Natl Acad. Sci. USA 93, 8699–8704 (1996).

    CAS  PubMed  PubMed Central  Google Scholar 

  115. Calabresi, P. et al. Tissue plasminogen activator controls multiple forms of synaptic plasticity and memory. Eur. J. Neurosci. 12, 1002–1012 (2000).

    CAS  PubMed  Google Scholar 

  116. Carmeliet, P. et al. Physiological consequences of loss of plasminogen activator gene function in mice. Nature 368, 419–424 (1994).

    CAS  PubMed  Google Scholar 

  117. Madani, R. et al. Enhanced hippocampal long-term potentiation and learning by increased neuronal expression of tissue-type plasminogen activator in transgenic mice. Embo J. 18, 3007–3012 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  118. Pang, P. T. et al. Cleavage of proBDNF by tPA/plasmin is essential for long-term hippocampal plasticity. Science 306, 487–491 (2004).

    CAS  PubMed  Google Scholar 

  119. Pang, P. T. & Lu, B. Regulation of late-phase LTP and long-term memory in normal and aging hippocampus: role of secreted proteins tPA and BDNF. Ageing Res. Rev. 3, 407–430 (2004).

    CAS  PubMed  Google Scholar 

  120. Nagappan, G. & Lu, B. Activity-dependent modulation of the BDNF receptor TrkB: mechanisms and implications. Trends Neurosci. 28, 464–471 (2005).

    CAS  PubMed  Google Scholar 

  121. Lynch, G., Rex, C. S., Chen, L. Y. & Gall, C. M. The substrates of memory: defects, treatments, and enhancement. Eur. J. Pharmacol. 585, 2–13 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  122. Schuster, C. M., Davis, G. W., Fetter, R. D. & Goodman, C. S. Genetic dissection of structural and functional components of synaptic plasticity. II. Fasciclin II controls presynaptic structural plasticity. Neuron 17, 655–667 (1996).

    CAS  PubMed  Google Scholar 

  123. Bailey, C. H. et al. Mutation in the phosphorylation sites of MAP kinase blocks learning-related internalization of apCAM in Aplysia sensory neurons. Neuron 18, 913–924 (1997).

    CAS  PubMed  Google Scholar 

  124. Han, J. H., Lim, C. S., Lee, Y. S., Kandel, E. R. & Kaang, B. K. Role of Aplysia cell adhesion molecules during 5-HT-induced long-term functional and structural changes. Learn. Mem. 11, 421–435 (2004).

    PubMed  PubMed Central  Google Scholar 

  125. Bailey, C. H., Chen, M., Keller, F. & Kandel, E. R. Serotonin-mediated endocytosis of apCAM: an early step of learning-related synaptic growth in Aplysia. Science 256, 645–649 (1992).

    CAS  PubMed  Google Scholar 

  126. Nakamura, K. et al. Enhancement of hippocampal LTP, reference memory and sensorimotor gating in mutant mice lacking a telencephalon-specific cell adhesion molecule. Eur. J. Neurosci. 13, 179–189 (2001).

    CAS  PubMed  Google Scholar 

  127. Cremer, H. et al. Inactivation of the N-CAM gene in mice results in size reduction of the olfactory bulb and deficits in spatial learning. Nature 367, 455–459 (1994).

    CAS  PubMed  Google Scholar 

  128. Law, J. W. et al. Decreased anxiety, altered place learning, and increased CA1 basal excitatory synaptic transmission in mice with conditional ablation of the neural cell adhesion molecule L1. J. Neurosci. 23, 10419–10432 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  129. Deuel, T. F., Zhang, N., Yeh, H. J., Silos-Santiago, I. & Wang, Z. Y. Pleiotrophin: a cytokine with diverse functions and a novel signaling pathway. Arch. Biochem. Biophys. 397, 162–171 (2002).

    CAS  PubMed  Google Scholar 

  130. Rauvala, H. & Peng, H. B. HB-GAM (heparin-binding growth-associated molecule) and heparin-type glycans in the development and plasticity of neuron-target contacts. Prog. Neurobiol. 52, 127–144 (1997).

    CAS  PubMed  Google Scholar 

  131. Pavlov, I. et al. Role of heparin-binding growth-associated molecule (HB-GAM) in hippocampal LTP and spatial learning revealed by studies on overexpressing and knockout mice. Mol. Cell Neurosci. 20, 330–342 (2002).

    CAS  PubMed  Google Scholar 

  132. Pavlov, I., Rauvala, H. & Taira, T. Enhanced hippocampal GABAergic inhibition in mice overexpressing heparin-binding growth-associated molecule. Neuroscience 139, 505–511 (2006).

    CAS  PubMed  Google Scholar 

  133. Humeau, Y., Shaban, H., Bissiere, S. & Luthi, A. Presynaptic induction of heterosynaptic associative plasticity in the mammalian brain. Nature 426, 841–845 (2003).

    CAS  PubMed  Google Scholar 

  134. Powell, C. M. et al. The presynaptic active zone protein RIM1alpha is critical for normal learning and memory. Neuron 42, 143–153 (2004).

    CAS  PubMed  PubMed Central  Google Scholar 

  135. Kushner, S. A. et al. Modulation of presynaptic plasticity and learning by the H-ras/extracellular signal-regulated kinase/synapsin I signaling pathway. J. Neurosci. 25, 9721–9734 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  136. Manabe, T. et al. Regulation of long-term potentiation by H-Ras through NMDA receptor phosphorylation. J. Neurosci. 20, 2504–2511 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  137. Martin, K. C. et al. MAP kinase translocates into the nucleus of the presynaptic cell and is required for long-term facilitation in Aplysia. Neuron 18, 899–912 (1997).

    CAS  PubMed  Google Scholar 

  138. Angers, A. et al. Serotonin stimulates phosphorylation of Aplysia synapsin and alters its subcellular distribution in sensory neurons. J. Neurosci. 22, 5412–5422 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  139. Rao, N., Dodge, I. & Band, H. The Cbl family of ubiquitin ligases: critical negative regulators of tyrosine kinase signaling in the immune system. J. Leukoc. Biol. 71, 753–763 (2002).

    CAS  PubMed  Google Scholar 

  140. Tan, D. P., Liu, Q. Y., Koshiya, N., Gu, H. & Alkon, D. Enhancement of long-term memory retention and short-term synaptic plasticity in cbl-b null mice. Proc. Natl Acad. Sci. USA 103, 5125–5130 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  141. Frankland, P. W. & Bontempi, B. The organization of recent and remote memories. Nature Rev. Neurosci. 6, 119–130 (2005).

    CAS  Google Scholar 

  142. Wiltgen, B. J., Brown, R. A., Talton, L. E. & Silva, A. J. New circuits for old memories: the role of the neocortex in consolidation. Neuron 44, 101–108 (2004). A comprehensive review of the molecular and cellular mechanisms underlying cortical memory consolidation.

    CAS  PubMed  Google Scholar 

  143. Haydon, P. G. GLIA: listening and talking to the synapse. Nature Rev. Neurosci. 2, 185–193 (2001).

    CAS  Google Scholar 

  144. McCall, M. A. et al. Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiology. Proc. Natl Acad. Sci. USA 93, 6361–6366 (1996).

    CAS  PubMed  PubMed Central  Google Scholar 

  145. Todd, K. J., Serrano, A., Lacaille, J. C. & Robitaille, R. Glial cells in synaptic plasticity. J. Physiol. Paris 99, 75–83 (2006).

    CAS  PubMed  Google Scholar 

  146. Zimmer, D. B., Cornwall, E. H., Landar, A. & Song, W. The S100 protein family: history, function, and expression. Brain Res. Bull. 37, 417–429 (1995).

    CAS  PubMed  Google Scholar 

  147. Gerlai, R., Wojtowicz, J. M., Marks, A. & Roder, J. Overexpression of a calcium-binding protein, S100 beta, in astrocytes alters synaptic plasticity and impairs spatial learning in transgenic mice. Learn. Mem. 2, 26–39 (1995).

    CAS  PubMed  Google Scholar 

  148. Nishiyama, H., Knopfel, T., Endo, S. & Itohara, S. Glial protein S100B modulates long-term neuronal synaptic plasticity. Proc. Natl Acad. Sci. USA 99, 4037–4042 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  149. Johnson, J. W. & Ascher, P. Glycine potentiates the NMDA response in cultured mouse brain neurons. Nature 325, 529–531 (1987).

    CAS  PubMed  Google Scholar 

  150. Martineau, M., Baux, G. & Mothet, J. P. D-serine signalling in the brain: friend and foe. Trends Neurosci. 29, 481–491 (2006).

    CAS  PubMed  Google Scholar 

  151. Maekawa, M., Watanabe, M., Yamaguchi, S., Konno, R. & Hori, Y. Spatial learning and long-term potentiation of mutant mice lacking D-amino-acid oxidase. Neurosci. Res. 53, 34–38 (2005).

    CAS  PubMed  Google Scholar 

  152. Birks, J. Cholinesterase inhibitors for Alzheimer's disease. Cochrane Database Syst. Rev. CD005593 (2006).

  153. Minzenberg, M. J. & Carter, C. S. Modafinil: a review of neurochemical actions and effects on cognition. Neuropsychopharmacology 33, 1477–1502 (2008).

    CAS  PubMed  Google Scholar 

  154. Harrell, A. V. & Allan, A. M. Improvements in hippocampal-dependent learning and decremental attention in 5-HT(3) receptor overexpressing mice. Learn. Mem. 10, 410–419 (2003).

    PubMed  PubMed Central  Google Scholar 

  155. Kim, J. J. et al. Selective enhancement of emotional, but not motor, learning in monoamine oxidase A-deficient mice. Proc. Natl Acad. Sci. USA 94, 5929–5933 (1997).

    CAS  PubMed  PubMed Central  Google Scholar 

  156. Haas, H. & Panula, P. The role of histamine and the tuberomamillary nucleus in the nervous system. Nature Rev. Neurosci. 4, 121–130 (2003).

    CAS  Google Scholar 

  157. Dere, E. et al. Histidine-decarboxylase knockout mice show deficient nonreinforced episodic object memory, improved negatively reinforced water-maze performance, and increased neo- and ventro-striatal dopamine turnover. Learn. Mem. 10, 510–519 (2003).

    PubMed  PubMed Central  Google Scholar 

  158. Liu, L. et al. Improved learning and memory of contextual fear conditioning and hippocampal CA1 long-term potentiation in histidine decarboxylase knock-out mice. Hippocampus 17, 634–641 (2007).

    CAS  PubMed  Google Scholar 

  159. Thompson, L. T., Moskal, J. R. & Disterhoft, J. F. Hippocampus-dependent learning facilitated by a monoclonal antibody or D-cycloserine. Nature 359, 638–641 (1992).

    CAS  PubMed  Google Scholar 

  160. Flood, J. F., Morley, J. E. & Lanthorn, T. H. Effect on memory processing by D-cycloserine, an agonist of the NMDA/glycine receptor. Eur. J. Pharmacol. 221, 249–254 (1992).

    CAS  PubMed  Google Scholar 

  161. Jones, R. W., Wesnes, K. A. & Kirby, J. Effects of NMDA modulation in scopolamine dementia. Ann. NY Acad. Sci. 640, 241–244 (1991).

    CAS  PubMed  Google Scholar 

  162. Neves, G., Cooke, S. F. & Bliss, T. V. Synaptic plasticity, memory and the hippocampus: a neural network approach to causality. Nature Rev. Neurosci. 9, 65–75 (2008). An up-to-date review discussing the relationship between synaptic plasticity and memory in the hippocampus.

    CAS  Google Scholar 

  163. Collinson, N. et al. Enhanced learning and memory and altered GABAergic synaptic transmission in mice lacking the alpha 5 subunit of the GABA(A) receptor. J. Neurosci. 22, 5572–5580 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  164. Murphy, G. G. et al. Increased neuronal excitability, synaptic plasticity, and learning in aged Kvbeta1.1 knockout mice. Curr. Biol. 14, 1907–1915 (2004).

    CAS  PubMed  Google Scholar 

  165. Gold, P. E. Coordination of multiple memory systems. Neurobiol. Learn. Mem. 82, 230–242 (2004).

    PubMed  Google Scholar 

  166. Fanselow, M. S. & Poulos, A. M. The neuroscience of mammalian associative learning. Annu. Rev. Psychol. 56, 207–234 (2005).

    PubMed  Google Scholar 

  167. Wei, F. et al. Genetic enhancement of inflammatory pain by forebrain NR2B overexpression. Nature Neurosci. 4, 164–169 (2001).

    CAS  PubMed  Google Scholar 

  168. Mehlman, M. J. Cognition-enhancing drugs. Milbank Q. 82, 483–506 (2004).

    PubMed  PubMed Central  Google Scholar 

  169. Tully, T., Bourtchouladze, R., Scott, R. & Tallman, J. Targeting the CREB pathway for memory enhancers. Nature Rev. Drug Discov. 2, 267–277 (2003).

    CAS  Google Scholar 

  170. Rose, S. P. 'Smart drugs': do they work? Are they ethical? Will they be legal? Nature Rev. Neurosci. 3, 975–979 (2002).

    CAS  Google Scholar 

  171. Farah, M. J. et al. Neurocognitive enhancement: what can we do and what should we do? Nature Rev. Neurosci. 5, 421–425 (2004). This review discusses the social and ethical aspects of neurocognitive enhancers.

    CAS  Google Scholar 

  172. Grant, S. G. et al. Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice. Science 258, 1903–1910 (1992).

    CAS  PubMed  Google Scholar 

  173. Mayford, M. & Kandel, E. R. Genetic approaches to memory storage. Trends Genet. 15, 463–470 (1999).

    CAS  PubMed  Google Scholar 

  174. Ohno, M., Frankland, P. W., Chen, A. P., Costa, R. M. & Silva, A. J. Inducible, pharmacogenetic approaches to the study of learning and memory. Nature Neurosci. 4, 1238–1243 (2001).

    CAS  PubMed  Google Scholar 

  175. Tsien, J. Z. et al. Subregion- and cell type-restricted gene knockout in mouse brain. Cell 87, 1317–1326 (1996).

    CAS  PubMed  Google Scholar 

  176. Mayford, M. et al. Control of memory formation through regulated expression of a CaMKII transgene. Science 274, 1678–1683 (1996). This study introduced the inducible transgenic doxycycline system to the study of cognitive mechanisms and addressed the role of CaMKII in memory formation.

    CAS  PubMed  Google Scholar 

  177. Chang, D. J. et al. Activation of a heterologously expressed octopamine receptor coupled only to adenylyl cyclase produces all the features of presynaptic facilitation in aplysia sensory neurons. Proc. Natl Acad. Sci. USA 97, 1829–1834 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  178. Wang, H. et al. Inducible protein knockout reveals temporal requirement of CaMKII reactivation for memory consolidation in the brain. Proc. Natl Acad. Sci. USA 100, 4287–4292 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  179. Zhang, F., Aravanis, A. M., Adamantidis, A., de Lecea, L. & Deisseroth, K. Circuit-breakers: optical technologies for probing neural signals and systems. Nature Rev. Neurosci. 8, 577–581 (2007).

    CAS  Google Scholar 

  180. Glaser, S., Anastassiadis, K. & Stewart, A. F. Current issues in mouse genome engineering. Nature Genet. 37, 1187–1193 (2005).

    CAS  PubMed  Google Scholar 

  181. Migaud, M. et al. Enhanced long-term potentiation and impaired learning in mice with mutant postsynaptic density-95 protein. Nature 396, 433–439 (1998).

    CAS  PubMed  Google Scholar 

  182. Jun, K. et al. Enhanced hippocampal CA1 LTP but normal spatial learning in inositol 1, 4, 5-trisphosphate 3-kinase(A)-deficient mice. Learn. Mem. 5, 317–330 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  183. Meng, Y. et al. Abnormal spine morphology and enhanced LTP in LIMK-1 knockout mice. Neuron 35, 121–133 (2002).

    CAS  PubMed  Google Scholar 

  184. Gu, Y. et al. Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice. J. Neurosci. 22, 2753–2763 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  185. Uetani, N. et al. Impaired learning with enhanced hippocampal long-term potentiation in PTPdelta-deficient mice. Embo J. 19, 2775–2785 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  186. Knuesel, I. et al. Short communication: altered synaptic clustering of GABAA receptors in mice lacking dystrophin (mdx mice). Eur. J. Neurosci. 11, 4457–4462 (1999).

    CAS  PubMed  Google Scholar 

  187. Rae, C. et al. Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse. Neuromuscul. Disord. 12, 121–129 (2002).

    PubMed  Google Scholar 

  188. Vaillend, C., Billard, J. M. & Laroche, S. Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin-deficient Dmd(mdx) mouse. Neurobiol. Dis. 17, 10–20 (2004).

    CAS  PubMed  Google Scholar 

  189. Futatsugi, A. et al. Facilitation of NMDAR-independent LTP and spatial learning in mutant mice lacking ryanodine receptor type 3. Neuron 24, 701–713 (1999).

    CAS  PubMed  Google Scholar 

  190. Jouvenceau, A. et al. Partial inhibition of PP1 alters bidirectional synaptic plasticity in the hippocampus. Eur. J. Neurosci. 24, 564–572 (2006).

    PubMed  Google Scholar 

  191. Routtenberg, A., Cantallops, I., Zaffuto, S., Serrano, P. & Namgung, U. Enhanced learning after genetic overexpression of a brain growth protein. Proc. Natl Acad. Sci. USA 97, 7657–7662 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  192. Holahan, M. R., Honegger, K. S., Tabatadze, N. & Routtenberg, A. GAP-43 gene expression regulates information storage. Learn. Mem. 14, 407–415 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  193. Shumyatsky, G. P. et al. Identification of a signaling network in lateral nucleus of amygdala important for inhibiting memory specifically related to learned fear. Cell 111, 905–918 (2002).

    CAS  PubMed  Google Scholar 

  194. Nolan, M. F. et al. A behavioral role for dendritic integration: HCN1 channels constrain spatial memory and plasticity at inputs to distal dendrites of CA1 pyramidal neurons. Cell 119, 719–732 (2004).

    CAS  PubMed  Google Scholar 

  195. Nolan, M. F. et al. The hyperpolarization-activated HCN1 channel is important for motor learning and neuronal integration by cerebellar Purkinje cells. Cell 115, 551–564 (2003).

    CAS  PubMed  Google Scholar 

  196. Slane, J. M., Lee, H. S., Vorhees, C. V., Zhang, J. H. & Xu, M. DNA fragmentation factor 45 deficient mice exhibit enhanced spatial learning and memory compared to wild-type control mice. Brain Res. 867, 70–79 (2000).

    CAS  PubMed  Google Scholar 

  197. McQuade, J. M., Vorhees, C. V., Xu, M. & Zhang, J. H. DNA fragmentation factor 45 knockout mice exhibit longer memory retention in the novel object recognition task compared to wild-type mice. Physiol. Behav. 76, 315–320 (2002).

    CAS  Google Scholar 

  198. Giese, K. P. et al. Reduced K+ channel inactivation, spike broadening, and after-hyperpolarization in Kv beta 1.1-deficient mice with impaired learning. Learn. Mem. 5, 257–273 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  199. Hu, D., Serrano, F., Oury, T. D. & Klann, E. Aging-dependent alterations in synaptic plasticity and memory in mice that overexpress extracellular superoxide dismutase. J. Neurosci. 26, 3933–3941 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  200. Thiels, E. et al. Impairment of long-term potentiation and associative memory in mice that overexpress extracellular superoxide dismutase. J. Neurosci. 20, 7631–7639 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We would like to thank members of the Silva laboratory for discussions that shaped this Review. We would like to give B. Dobkin a special thanks for his enthusiasm for this project, the Adelson Foundation, Korea Research Foundation (KRF-2007-357-C00101), NIA (AG13622), NINDS (NS38480) and NIMH (MH077972) for funding that made this work possible.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alcino J. Silva.

Related links

Related links

DATABASES

OMIM

Alzheimer's disease

Parkinson's disease

FURTHER INFORMATION

Genes to Cognition programme

Alcino J. Silva's homepage

Glossary

Rubinstein-Taybe syndrome

Rubinstein-Taybe syndrome is a genetic disorder that occurs in 1/125,000 births and is characterized by mental retardation, broad thumbs and toes, and facial abnormalities. It can be caused by heterozygous mutations in CREB binding protein (CBP).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lee, YS., Silva, A. The molecular and cellular biology of enhanced cognition. Nat Rev Neurosci 10, 126–140 (2009). https://doi.org/10.1038/nrn2572

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrn2572

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing