Environmental enrichment preserves a young DNA methylation landscape in the aged mouse hippocampus.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
23 06 2021
Historique:
received: 19 09 2019
accepted: 20 05 2021
entrez: 24 6 2021
pubmed: 25 6 2021
medline: 20 7 2021
Statut: epublish

Résumé

The decline of brain function during aging is associated with epigenetic changes, including DNA methylation. Lifestyle interventions can improve brain function during aging, but their influence on age-related epigenetic changes is unknown. Using genome-wide DNA methylation sequencing, we here show that experiencing a stimulus-rich environment counteracts age-related DNA methylation changes in the hippocampal dentate gyrus of mice. Specifically, environmental enrichment prevented the aging-induced CpG hypomethylation at target sites of the methyl-CpG-binding protein Mecp2, which is critical to neuronal function. The genes at which environmental enrichment counteracted aging effects have described roles in neuronal plasticity, neuronal cell communication and adult hippocampal neurogenesis and are dysregulated with age-related cognitive decline in the human brain. Our results highlight the stimulating effects of environmental enrichment on hippocampal plasticity at the level of DNA methylation and give molecular insights into the specific aspects of brain aging that can be counteracted by lifestyle interventions.

Identifiants

pubmed: 34162876
doi: 10.1038/s41467-021-23993-1
pii: 10.1038/s41467-021-23993-1
pmc: PMC8222384
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3892

Références

Phillips, C. Lifestyle modulators of neuroplasticity: how physical activity, mental engagement, and diet promote cognitive health during aging. Neural Plast 2017, 3589271 (2017).
Fratiglioni, L., Paillard-Borg, S. & Winblad, B. An active and socially integrated lifestyle in late life might protect against dementia. Lancet Neurol. 3, 343–353 (2004).
pubmed: 15157849 doi: 10.1016/S1474-4422(04)00767-7
Verghese, J. et al. Leisure activities and the risk of dementia in the elderly. N. Engl. J. Med. 348, 2508–2516 (2003).
pubmed: 12815136 doi: 10.1056/NEJMoa022252
Hertzog, C., Kramer, A. F., Wilson, R. S. & Lindenberger, U. Enrichment effects on adult cognitive development: can the functional capacity of older adults be preserved and enhanced?. Psychol Sci Public Interest 9, 1–65 (2008).
pubmed: 26162004 doi: 10.1111/j.1539-6053.2009.01034.x
Cabeza, R. et al. Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing. Nat. Rev. Neurosci. 19, 701–710 (2018).
pubmed: 30305711 pmcid: 6472256 doi: 10.1038/s41583-018-0068-2
Stern, Y. et al. Whitepaper: Defining and investigating cognitive reserve, brain reserve, and brain maintenance. Alzheimer’s Dement. 16, 1305–1311 (2018).
doi: 10.1016/j.jalz.2018.07.219
Kempermann, G. Environmental enrichment, new neurons and the neurobiology of individuality. Nat. Rev. Neurosci. 20, 235–245 (2019).
pubmed: 30723309 doi: 10.1038/s41583-019-0120-x
Redolat, R. & Mesa-Gresa, P. Potential benefits and limitations of enriched environments and cognitive activity on age-related behavioural decline. Curr. Top. Behav. Neurosci. 10, 293–316 (2012).
pubmed: 21643900 doi: 10.1007/7854_2011_134
Nithianantharajah, J. & Hannan, A. J. The neurobiology of brain and cognitive reserve: mental and physical activity as modulators of brain disorders. Prog. Neurobiol. 89, 369–382 (2009).
pubmed: 19819293 doi: 10.1016/j.pneurobio.2009.10.001
Sale, A., Berardi, N. & Maffei, L. Enrich the environment to empower the brain. Trends Neurosci. 32, 233–239 (2009).
pubmed: 19268375 doi: 10.1016/j.tins.2008.12.004
Van Praag, H., Kempermann, G. & Gage, F. H. Neural consequences of environmental enrichment. Nat. Rev. Neurosci. 1, 191–198 (2000).
pubmed: 11257907 doi: 10.1038/35044558
Kempermann, G., Kuhn, H. G. & Gage, F. H. More hippocampal neurons in adult mice living in an enriched environment. Nature 386, 493–495 (1997).
pubmed: 9087407 doi: 10.1038/386493a0
Fan, X., Wheatley, E. G. & Villeda, S. A. Mechanisms of hippocampal aging and the potential for rejuvenation. Annu. Rev. Neurosci. 40, 251–272 (2017).
pubmed: 28441118 doi: 10.1146/annurev-neuro-072116-031357
Sampedro-Piquero, P. & Begega, A. Environmental enrichment as a positive behavioral intervention across the lifespan. Curr. Neuropharmacol. 15, 459–470 (2017).
pubmed: 27012955 pmcid: 5543669 doi: 10.2174/1570159X14666160325115909
Körholz, J. C. et al. Selective increases in inter-individual variability in response to environmental enrichment in female mice. Elife 7, e35690 (2018).
pubmed: 30362941 doi: 10.7554/eLife.35690 pmcid: 6203437
Garthe, A., Roeder, I. & Kempermann, G. Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis. Hippocampus 26, 261–271 (2016).
pubmed: 26311488 doi: 10.1002/hipo.22520
Fischer, A. Environmental enrichment as a method to improve cognitive function. What can we learn from animal models? Neuroimage 131, 42–47 (2016).
pubmed: 26656208 doi: 10.1016/j.neuroimage.2015.11.039
Nithianantharajah, J. & Hannan, A. J. Enriched environments, experience-dependent plasticity and disorders of the nervous system. Nat. Rev. Neurosci. 7, 697–709 (2006).
pubmed: 16924259 doi: 10.1038/nrn1970
Clemenson, G. D. et al. Environmental enrichment and neuronal plasticity. in The Oxford Handbook of Developmental Neural Plasticity https://doi.org/10.1093/oxfordhb/9780190635374.013.13 (2018).
Kempermann, G., Kuhn, H. G. & Gage, F. H. Experience-induced neurogenesis in the senescent dentate gyrus. J. Neurosci. 18, 3206–3212 (1998).
pubmed: 9547229 pmcid: 6792643 doi: 10.1523/JNEUROSCI.18-09-03206.1998
Kempermann, G., Gast, D. & Gage, F. H. Neuroplasticity in old age: sustained fivefold induction of hippocampal neurogenesis by long-term environmental enrichment. Ann. Neurol. 52, 135–143 (2002).
pubmed: 12210782 doi: 10.1002/ana.10262
Speisman, R. B. et al. Environmental enrichment restores neurogenesis and rapid acquisition in aged rats. Neurobiol. Aging 34, 263–274 (2013).
pubmed: 22795793 doi: 10.1016/j.neurobiolaging.2012.05.023
Darmopil, S., Petanjek, Z., Mohammed, A. H. & Bogdanović, N. Environmental enrichment alters dentate granule cell morphology in oldest-old rat. J. Cell. Mol. Med. 13, 1845–1856 (2009).
pubmed: 19175692 doi: 10.1111/j.1582-4934.2008.00560.x
Griñan-Ferré, C. et al. Environmental enrichment improves behavior, cognition, and brain functional markers in young senescence-accelerated prone mice (SAMP8). Mol. Neurobiol. 53, 2435–2450 (2016).
pubmed: 26014386 doi: 10.1007/s12035-015-9210-6
Blasco, M. A., Partridge, L., Serrano, M., Kroemer, G. & Lo, C. The hallmarks of aging. Cell 153, 1194–1217 (2013).
pubmed: 23746838 pmcid: 3836174 doi: 10.1016/j.cell.2013.05.039
Horvath, S. DNA methylation age of human tissues and cell types. Genome Biol. 14, R115 (2013).
pubmed: 24138928 doi: 10.1186/gb-2013-14-10-r115 pmcid: 4015143
Oliveira, A. M. M., Hemstedt, T. J. & Bading, H. Rescue of aging-associated decline in Dnmt3a2 expression restores cognitive abilities. Nat. Neurosci. 15, 1111–1113 (2012).
pubmed: 22751036 doi: 10.1038/nn.3151
Gontier, G. et al. Tet2 rescues age-related regenerative decline and enhances cognitive function in the adult mouse brain. Cell Rep. 22, 2094–2106 (2018).
doi: 10.1016/j.celrep.2018.02.001
Kaas, G. A. et al. TET1 controls CNS 5-methylcytosine hydroxylation, active DNA demethylation, gene transcription, and memory formation. Neuron 79, 1086–1093 (2013).
pubmed: 24050399 doi: 10.1016/j.neuron.2013.08.032
Feng, J. et al. Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons. Nat. Neurosci. 13, 423–430 (2010).
pubmed: 20228804 pmcid: 3060772 doi: 10.1038/nn.2514
Nelson, E. D., Kavalali, E. T. & Monteggia, L. M. Activity-dependent suppression of miniature neurotransmission through the regulation of DNA methylation. J. Neurosci. 28, 395–406 (2008).
pubmed: 18184782 pmcid: 6670512 doi: 10.1523/JNEUROSCI.3796-07.2008
Weaver, I. C. G. et al. Epigenetic programming by maternal behavior. Nat. Neurosci. 7, 847–54 (2004).
pubmed: 15220929 doi: 10.1038/nn1276
Halder, R. et al. DNA methylation changes in plasticity genes accompany the formation and maintenance of memory. Nat. Neurosci. 19, 102–110 (2016).
pubmed: 26656643 doi: 10.1038/nn.4194
Guo, J. U. et al. Neuronal activity modifies the DNA methylation landscape in the adult brain. Nat. Neurosci. 14, 1345–1351 (2011).
pubmed: 21874013 pmcid: 3183401 doi: 10.1038/nn.2900
Cholewa-Waclaw, J. et al. The role of epigenetic mechanisms in the regulation of gene expression in the nervous system. J. Neurosci. 36, 11427–11434 (2016).
pubmed: 27911745 pmcid: 5125210 doi: 10.1523/JNEUROSCI.2492-16.2016
Masser, D. R. et al. Sexually divergent DNA methylation patterns with hippocampal aging. Aging Cell 16, 1342–1352 (2017).
pubmed: 28948711 pmcid: 5676057 doi: 10.1111/acel.12681
Penner, M. R. et al. Age-related changes in Egr1 transcription and DNA methylation within the hippocampus. Hippocampus 26, 1008–20 (2016).
pubmed: 26972614 pmcid: 4949137 doi: 10.1002/hipo.22583
Li, P. et al. Epigenetic dysregulation of enhancers in neurons is associated with Alzheimer’s disease pathology and cognitive symptoms. Nat. Commun. 10, 2246 (2019).
pubmed: 31113950 doi: 10.1038/s41467-019-10101-7 pmcid: 6529540
Gasparoni, G. et al. DNA methylation analysis on purified neurons and glia dissects age and Alzheimer’s disease-specific changes in the human cortex. Epigenetics Chromatin 11, 41 (2018).
pubmed: 30045751 pmcid: 6058387 doi: 10.1186/s13072-018-0211-3
Zhang, W., Qu, J., Liu, G. H. & Belmonte, J. C. I. The ageing epigenome and its rejuvenation. Nat. Rev. Mol. Cell Biol. 21, 137–150 (2020).
pubmed: 32020082 doi: 10.1038/s41580-019-0204-5
Zhang, T. Y. et al. Environmental enrichment increases transcriptional and epigenetic differentiation between mouse dorsal and ventral dentate gyrus. Nat. Commun. 9, 1–11 (2018).
Irier, H. et al. Environmental enrichment modulates 5-hydroxymethylcytosine dynamics in hippocampus. Genomics 104, 376–382 (2014).
pubmed: 25205305 doi: 10.1016/j.ygeno.2014.08.019
Fischer, A., Sananbenesi, F., Wang, X., Dobbin, M. & Tsai, L. Recovery of learning and memory is associated with chromatin remodelling. Nature 447, 178–183 (2007).
pubmed: 17468743 doi: 10.1038/nature05772
Meissner, A. et al. Reduced representation bisulfite sequencing for comparative high-resolution DNA methylation analysis. Nucleic Acids Res. 33, 5868–5877 (2005).
pubmed: 16224102 pmcid: 1258174 doi: 10.1093/nar/gki901
Boyle, P. et al. Gel-free multiplexed reduced representation bisulfite sequencing for large-scale DNA methylation profiling. Genome Biol. 13, R92 (2012).
pubmed: 23034176 doi: 10.1186/gb-2012-13-10-r92 pmcid: 3491420
The Gene Ontology Consortium. The gene ontology resource: 20 years and still going strong. Nucleic Acids Res. 47, D330–D338 (2019).
Fabregat, A. et al. The reactome pathway knowledgebase. Nucleic Acid Res. 46, 649–655 (2018).
doi: 10.1093/nar/gkx1132
Overall, R. W., Paszkowski-Rogacz, M. & Kempermann, G. The mammalian adult neurogenesis gene ontology (MANGO) provides a structural framework for published information on genes regulating adult hippocampal neurogenesis. PLoS ONE 7, e48527 (2012).
Koopmans, F. et al. SynGO: an evidence-based, expert-curated knowledge base for the synapse. Neuron 103, 217–234 (2019).
pubmed: 31171447 pmcid: 6764089 doi: 10.1016/j.neuron.2019.05.002
Bloodgood, B. L., Sharma, N., Browne, H. A., Trepman, A. Z. & Greenberg, M. E. The activity-dependent transcription factor NPAS4 regulates domain-specific inhibition. Nature 503, 121–125 (2013).
pubmed: 24201284 pmcid: 4169177 doi: 10.1038/nature12743
Singhal, G. et al. Effects of aging on the motor, cognitive and affective behaviors, neuroimmune responses and hippocampal gene expression. Behav. Brain Res. 383, 112501 (2020).
pubmed: 31987935 doi: 10.1016/j.bbr.2020.112501
Cizeron, M. et al. A brain-wide atlas of synapses across the mouse lifespan. Science 275, eaba3163 (2020).
Hadad, N. et al. Caloric restriction mitigates age-associated hippocampal differential CG and non-CG methylation. Neurobiol. Aging 67, 53–66 (2018).
pubmed: 29631215 pmcid: 5955819 doi: 10.1016/j.neurobiolaging.2018.03.009
Rinaldi, L. et al. Dnmt3a and Dnmt3b associate with enhancers to regulate human epidermal stem cell homeostasis. Cell Stem Cell 19, 491–501 (2016).
pubmed: 27476967 doi: 10.1016/j.stem.2016.06.020
Nan, X., Campoy, F. J. & Bird, A. MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin. Cell 88, 471–481 (1997).
pubmed: 9038338 doi: 10.1016/S0092-8674(00)81887-5
Gabel, H. W. et al. Disruption of DNA-methylation-dependent long gene repression in Rett syndrome. Nature 522, 89–93 (2015).
pubmed: 25762136 pmcid: 4480648 doi: 10.1038/nature14319
Merico, D., Isserlin, R., Stueker, O., Emili, A. & Bader, G. D. Enrichment map: a network-based method for gene-set enrichment visualization and interpretation. PLoS ONE 5, e13984 (2010).
pubmed: 21085593 doi: 10.1371/journal.pone.0013984 pmcid: 2981572
Su, Y. et al. Neuronal activity modifies the chromatin accessibility landscape in the adult brain. Nat. Neurosci. 20, 476–483 (2017).
pubmed: 28166220 pmcid: 5325677 doi: 10.1038/nn.4494
Karaca, K. G., Brito, D. V. C. & Oliveira, A. M. M. MeCP2: a critical regulator of chromatin in neurodevelopment and adult brain function. Int. J. Mol. Sci. 20, 4577 (2019).
doi: 10.3390/ijms20184577
Rao, S., Kay, Y. & Herring, B. E. Tiam1 is critical for glutamatergic synapse structure and function in the hippocampus. J. Neurosci. 39, 9306–9315 (2019).
pubmed: 31597723 pmcid: 6867819 doi: 10.1523/JNEUROSCI.1566-19.2019
Rube, H. T. et al. Sequence features accurately predict genome-wide MeCP2 binding in vivo. Nat. Commun. 7, 1–12 (2016).
doi: 10.1038/ncomms11025
Tillotson, R. & Bird, A. The molecular basis of MeCP2 function in the brain. J. Mol. Biol. 432, 1602–1623 (2020).
doi: 10.1016/j.jmb.2019.10.004
Weiss, L. A. & Nieto, M. The crux of Cux genes in neuronal function and plasticity. Brain Res. 32–42, 2019 (1705).
Zhang, T. Y. et al. Environmental enrichment increases transcriptional and epigenetic differentiation between mouse dorsal and ventral dentate gyrus. Nat. Commun. 9, 298 (2018).
pubmed: 29352183 doi: 10.1038/s41467-017-02748-x pmcid: 5775256
Mostafavi, S. et al. A molecular network of the aging human brain provides insights into the pathology and cognitive decline of Alzheimer’s disease. Nat. Neurosci. 21, 811–819 (2018).
pubmed: 29802388 pmcid: 6599633 doi: 10.1038/s41593-018-0154-9
Wingo, A. P. et al. Large-scale proteomic analysis of human brain identifies proteins associated with cognitive trajectory in advanced age. Nat. Commun. 10, 1619 (2019).
pubmed: 30962425 doi: 10.1038/s41467-019-09613-z pmcid: 6453881
Maegawa, S. et al. Caloric restriction delays age-related methylation drift. Nat. Commun. 8, 539 (2017).
pubmed: 28912502 doi: 10.1038/s41467-017-00607-3 pmcid: 5599616
Stroud, H. et al. Early-life gene expression in neurons modulates lasting epigenetic states. Cell 171, 1151–1154 (2017).
pubmed: 29056337 pmcid: 5693680 doi: 10.1016/j.cell.2017.09.047
Lewis, J. D. et al. Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA. Cell 69, 905–914 (1992).
pubmed: 1606614 doi: 10.1016/0092-8674(92)90610-O
Gabel, H. W. et al. Disruption of DNA-methylation-dependent long gene repression in Rett syndrome. Nature 522, 89–93 (2015).
pubmed: 25762136 pmcid: 4480648 doi: 10.1038/nature14319
Kinde, B., Wu, D. Y., Greenberg, M. E. & Gabel, H. W. DNA methylation in the gene body influences MeCP2-mediated gene repression. Proc. Natl Acad. Sci. USA 113, 15114–15119 (2016).
pubmed: 27965390 doi: 10.1073/pnas.1618737114 pmcid: 5206576
Guy, J., Cheval, H., Selfridge, J. & Bird, A. The role of MeCP2 in the brain. Annu. Rev. Cell Dev. Biol. 27, 631–652 (2011).
pubmed: 21721946 doi: 10.1146/annurev-cellbio-092910-154121
Ip, J. P. K., Mellios, N. & Sur, M. Rett syndrome: insights into genetic, molecular and circuit mechanisms. Nat. Rev. Neurosci. 19, 368–382 (2018).
pubmed: 29740174 pmcid: 6402579 doi: 10.1038/s41583-018-0006-3
Li, H. et al. Cell cycle-linked MeCP2 phosphorylation modulates adult neurogenesis involving the Notch signalling pathway. Nat. Commun. 5, 5601 (2014).
pubmed: 25420914 doi: 10.1038/ncomms6601
Osenberg, S. et al. Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome. Proc. Natl Acad. Sci. USA 115, E5363–E5372 (2018).
pubmed: 29769330 doi: 10.1073/pnas.1722546115 pmcid: 6003366
Stilling, R. M. et al. De-regulation of gene expression and alternative splicing affects distinct cellular pathways in the aging hippocampus. Front. Cell. Neurosci. 373, 1–15 (2014).
Zhao, B. et al. Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals. PLoS Genet 15, e1008043 (2019).
pubmed: 30973874 doi: 10.1371/journal.pgen.1008043 pmcid: 6478352
Cardelli, M. The epigenetic alterations of endogenous retroelements in aging. Mech. Ageing Dev. 174, 30–46 (2018).
pubmed: 29458070 doi: 10.1016/j.mad.2018.02.002
Rampon, C. et al. Effects of environmental enrichment on gene expression in the brain. PNAS 97, 12880–12884 (2000).
pubmed: 11070096 doi: 10.1073/pnas.97.23.12880 pmcid: 18858
Zhang, Y. et al. Transcriptomics of environmental enrichment reveals a role for retinoic acid signaling in addiction. Front. Mol. Neurosci. 9, 119 (2016).
Sahay, A. et al. Increasing adult hippocampal neurogenesis is sufficient to improve pattern separation. Nature 472, 466–470 (2011).
pubmed: 21460835 pmcid: 3084370 doi: 10.1038/nature09817
Kempermann, G. & Gage, F. H. Experience-dependent regulation of adult hippocampal neurogenesis: effects of long-term stimulation and stimulus withdrawal. Hippocampus 9, 321–332 (1999).
pubmed: 10401646 doi: 10.1002/(SICI)1098-1063(1999)9:3<321::AID-HIPO11>3.0.CO;2-C
Ben Abdallah, N. M. B., Slomianka, L., Vyssotski, A. L. & Lipp, H. P. Early age-related changes in adult hippocampal neurogenesis in C57 mice. Neurobiol. Aging 31, 151–161 (2010).
pubmed: 18455269 doi: 10.1016/j.neurobiolaging.2008.03.002
Kempermann, G. Environmental enrichment, new neurons and the neurobiology of individuality. Nat. Rev. Neurosci. 20, 235–245 (2019).
Jaeger, B. N. et al. A novel environment-evoked transcriptional signature predicts reactivity in single dentate granuel neurons. Nat. Commun. 9, 3084 (2018).
pubmed: 30082781 doi: 10.1038/s41467-018-05418-8 pmcid: 6079101
Fernandez-Albert, J. et al. Immediate and deferred epigenomic signatures of in vivo neuronal activation in mouse hippocampus. Nat. Neurosci. 22, 1–13 (2019).
doi: 10.1038/s41593-019-0476-2
Li, R. et al. Mapping accumulative whole-brain activities during environmental enrichment with manganese-enhanced magnetic resonance imaging. Neuroimage 210, 116588 (2020).
pubmed: 32004718 doi: 10.1016/j.neuroimage.2020.116588
Harris, C. J. et al. Age-associated DNA methylation patterns are shared between the hippocampus and peripheral blood cells. Front. Genet. 11, 111 (2020).
pubmed: 32211019 doi: 10.3389/fgene.2020.00111 pmcid: 7067920
Cortese, G. P., Olin, A., O’Riordan, K., Hullinger, R. & Burger, C. Environmental enrichment improves hippocampal function in aged rats by enhancing learning and memory, LTP, and mGluR5-Homer1c activity. Neurobiol. Aging 63, 1–11 (2018).
pubmed: 29207276 doi: 10.1016/j.neurobiolaging.2017.11.004
Krueger, F. & Andrews, S. R. Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications. Bioinformatics 27, 1571–1572 (2011).
pubmed: 21493656 doi: 10.1093/bioinformatics/btr167 pmcid: 3102221
Akalin, A. et al. methylKit: a comprehensive R package for the analysis of genome-wide DNA methylation profiles. Genome Biol. 13, R87 (2012).
pubmed: 23034086 doi: 10.1186/gb-2012-13-10-r87 pmcid: 3491415
Kinsella, R. J. et al. Ensembl BioMarts: a hub for data retrieval across taxonomic space. Database 2011, bar03 (2011).
doi: 10.1093/database/bar030
Pagès, H., Carlson, M., Falcon, S. & Li, N. AnnotationDbi: Annotation Database Interface. R package version 1.42.1. (2018).
Karolchik, D. et al. The UCSC table browser data retrieval tool. Nucleic Acids Res 32, 493–496 (2004).
doi: 10.1093/nar/gkh103
Zerbino, D. R., Wilder, S. P., Johnson, N., Juettemann, T. & Flicek, P. R. The ensembl regulatory build. Genome Biol. 16, 1–8 (2015).
doi: 10.1186/s13059-015-0621-5
Khan, A. & Zhang, X. dbSUPER: a database of super-enhancers in mouse and human genome. Nucleic Acids Res 44, D164–71 (2016).
pubmed: 26438538 doi: 10.1093/nar/gkv1002
Lawrence, M. et al. Software for computing and annotating genomic ranges. PLoS Comput. Biol. 9, 1–10 (2013).
doi: 10.1371/journal.pcbi.1003118
Shannon, P. & Richards, M. MotifDb: An Annotated Collection of Protein-DNA Binding Sequence Motifs. R Package version 1.26.0. (2019).
Mclean, C. Y. et al. GREAT improves functional interpretation of cis-regulatory regions. Nat. Biotechnol. 28, 495–501 (2010).
pubmed: 20436461 pmcid: 4840234 doi: 10.1038/nbt.1630
Yu, G. & He, Q. Molecular BioSystems Reactome PA: an R/Bioconductor package for reactome pathway analysis and visualization. Mol. Biosyst. 12, 477–479 (2016).
pubmed: 26661513 doi: 10.1039/C5MB00663E
Stubbs, T. M. et al. Multi-tissue DNA methylation age predictor in mouse. Genome Biol. 18 (2017).
Thompson, M. J. et al. A multi-tissue full lifespan epigenetic clock for mice. Aging 10, 2832–2854 (2018).
pubmed: 30348905 pmcid: 6224226 doi: 10.18632/aging.101590

Auteurs

Sara Zocher (S)

German Center for Neurodegenerative Diseases (DZNE) Dresden, Dresden, Germany.
Center for Regenerative Therapies Dresden (CRTD), Technische Universität Dresden, Dresden, Germany.

Rupert W Overall (RW)

German Center for Neurodegenerative Diseases (DZNE) Dresden, Dresden, Germany.
Center for Regenerative Therapies Dresden (CRTD), Technische Universität Dresden, Dresden, Germany.

Mathias Lesche (M)

Center for Regenerative Therapies Dresden (CRTD), Technische Universität Dresden, Dresden, Germany.
DRESDEN-concept Genome Center c/o Center for Molecular and Cellular Bioengineering (CMCB), Technische Universität Dresden, Dresden, Germany.

Andreas Dahl (A)

Center for Regenerative Therapies Dresden (CRTD), Technische Universität Dresden, Dresden, Germany.
DRESDEN-concept Genome Center c/o Center for Molecular and Cellular Bioengineering (CMCB), Technische Universität Dresden, Dresden, Germany.

Gerd Kempermann (G)

German Center for Neurodegenerative Diseases (DZNE) Dresden, Dresden, Germany. Gerd.Kempermann@dzne.de.
Center for Regenerative Therapies Dresden (CRTD), Technische Universität Dresden, Dresden, Germany. Gerd.Kempermann@dzne.de.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH