- Brief Communication
- Published:
Rescue of aging-associated decline in Dnmt3a2 expression restores cognitive abilities
Nature Neurosciencevolume 15, pages1111–1113 (2012)Cite this article
7161Accesses
279Citations
38Altmetric
Abstract
Cognitive abilities decline in normal aging, yet the underlying molecular mechanisms are poorly understood. We found that aging was associated with a decrease in the expression of the DNA methyltransferase Dnmt3a2 in the hippocampus and that rescuing Dnmt3a2 levels restored cognitive functions. Moreover, we found thatDnmt3a2 is an activity-regulated immediate early gene that is partly dependent on nuclear calcium signaling and that hippocampal Dnmt3a2 levels determine cognitive abilities in both young adult and aged mice.
This is a preview of subscription content,access via your institution
Access options
Subscription info for Japanese customers
We have a dedicated website for our Japanese customers. Please go tonatureasia.com to subscribe to this journal.
Buy this article
- Purchase on SpringerLink
- Instant access to the full article PDF.
¥ 4,980
Prices may be subject to local taxes which are calculated during checkout


Similar content being viewed by others
References
Klose, R.J. & Bird, A.P.Trends Biochem. Sci.31, 89–97 (2006).
Suzuki, M.M. & Bird, A.Nat. Rev. Genet.9, 465–476 (2008).
Guo, J.U. et al.Nat. Neurosci.14, 1345–1351 (2011).
Miller, C.A. & Sweatt, J.D.Neuron53, 857–869 (2007).
Feng, J. et al.Nat. Neurosci.13, 423–430 (2010).
Monsey, M.S., Ota, K.T., Akingbade, I.F., Hong, E.S. & Schafe, G.E.PLoS ONE6, e19958 (2011).
Vanyushin, B.F., Nemirovsky, L.E., Klimenko, V.V., Vasiliev, V.K. & Belozersky, A.N.Gerontologia19, 138–152 (1973).
Wilson, V.L., Smith, R.A., Ma, S. & Cutler, R.G.J. Biol. Chem.262, 9948–9951 (1987).
Fuke, C. et al.Ann. Hum. Genet.68, 196–204 (2004).
Chen, T., Ueda, Y., Xie, S. & Li, E.J. Biol. Chem.277, 38746–38754 (2002).
Kotini, A.G., Mpakali, A. & Agalioti, T.Mol. Cell. Biol.31, 1577–1592 (2011).
Kang, Y.K. et al.FEBS Lett.498, 1–5 (2001).
Erickson, C.A. & Barnes, C.A.Exp. Gerontol.38, 61–69 (2003).
Chahrour, M. et al.Science320, 1224–1229 (2008).
Zhang, S.J. et al.PLoS Genet.5, e1000604 (2009).
Bading, H. & Greenberg, M.E.Science253, 912–914 (1991).
Hardingham, G.E., Chawla, S., Johnson, C.M. & Bading, H.Nature385, 260–265 (1997).
Klugmann, M. et al.Mol. Cell. Neurosci.28, 347–360 (2005).
Sholl, D.A.J. Anat.87, 387–406 (1953).
Acknowledgements
We thank I. Bünzli-Ehret for her help with the preparation of hippocampal cultures and U. Weiss for the western blot experiments. We thank D. Tkachev and M. Klugmann for their contributions at the initial stages of this project and the tools that they provided. We thank A.M. Hagenston for comments on the manuscript. This work was supported by the Alexander von Humboldt Foundation (Wolfgang Paul Prize to H.B.), an ERC Advanced Grant (to H.B.), the Sonderforschungsbereich (SFB) 488 and SFB 636 of the Deutsche Forschungsgemeinschaft. H.B. is a member of the Excellence Cluster CellNetworks at Heidelberg University. A.M.M.O. is recipient of a Postdoctoral Fellowship by the Foundation for Science and Technology, Portugal.
Author information
Authors and Affiliations
Department of Neurobiology, Interdisciplinary Centre for Neurosciences (IZN), University of Heidelberg, Heidelberg, Germany
Ana M M Oliveira, Thekla J Hemstedt & Hilmar Bading
- Ana M M Oliveira
Search author on:PubMed Google Scholar
- Thekla J Hemstedt
Search author on:PubMed Google Scholar
- Hilmar Bading
Search author on:PubMed Google Scholar
Contributions
A.M.M.O. and H.B. conceived the project and designed the experiments. A.M.M.O. and T.J.H. performed the experiments. A.M.M.O. and H.B. wrote the manuscript.
Corresponding author
Correspondence toHilmar Bading.
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Supplementary information
Supplementary Text and Figures
Supplementary Figures 1–7 (PDF 21445 kb)
Rights and permissions
About this article
Cite this article
Oliveira, A., Hemstedt, T. & Bading, H. Rescue of aging-associated decline in Dnmt3a2 expression restores cognitive abilities.Nat Neurosci15, 1111–1113 (2012). https://doi.org/10.1038/nn.3151
Received:
Accepted:
Published:
Issue date:
Share this article
Anyone you share the following link with will be able to read this content:
Sorry, a shareable link is not currently available for this article.
Provided by the Springer Nature SharedIt content-sharing initiative
This article is cited by
Assessing cognitive decline in the aging brain: lessons from rodent and human studies
- D. V. C. Brito
- F. Esteves
- C. Nóbrega
npj Aging (2023)
Neuroepigenetic Changes in DNA Methylation Affecting Diabetes-Induced Cognitive Impairment
- Valencia Fernandes
- Kumari Preeti
- Shashi Bala Singh
Cellular and Molecular Neurobiology (2023)
Pathophysiological Aspects and Therapeutic Armamentarium of Alzheimer’s Disease: Recent Trends and Future Development
- Bhavarth P. Dave
- Yesha B. Shah
- Mehul R. Chorawala
Cellular and Molecular Neurobiology (2023)
Genomic targets and selective inhibition of DNA methyltransferase isoforms
- Chanachai Sae-Lee
- Timothy M. Barrow
- Hyang-Min Byun
Clinical Epigenetics (2022)
Roles of physical exercise in neurodegeneration: reversal of epigenetic clock
- Miao Xu
- JiaYi Zhu
- Nan-Jie Xu
Translational Neurodegeneration (2021)


