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The transcriptional landscape of age in human peripheral blood

التفاصيل البيبلوغرافية
العنوان: The transcriptional landscape of age in human peripheral blood
المؤلفون: Peters, MJ, Joehanes, R, Pilling, LC, Schurmann, C, Conneely, KN, Powell, J, Reinmaa, E, Sutphin, GL, Zhernakova, A, Schramm, K, Wilson, YA, Kobes, S, Tukiainen, T, Ramos, YF, Göring, HHH, Fornage, M, Liu, Y, Gharib, SA, Stranger, BE, De Jager, PL, Aviv, A, Levy, D, Murabito, JM, Munson, PJ, Huan, T, Hofman, A, Uitterlinden, AG, Rivadeneira, F, Van Rooij, J, Stolk, L, Broer, L, Verbiest, MMPJ, Jhamai, M, Arp, P, Metspalu, A, Tserel, L, Milani, L, Samani, NJ, Peterson, P, Kasela, S, Codd, V, Peters, A, Ward-Caviness, CK, Herder, C, Waldenberger, M, Roden, M, Singmann, P, Zeilinger, S, Illig, T, Homuth, G, Grabe, HJ, Völzke, H, Steil, L, Kocher, T, Murray, A, Melzer, D, Yaghootkar, H, Bandinelli, S, Moses, EK, Kent, JW, Curran, JE, Johnson, MP, Williams-Blangero, S, Westra, HJ, McRae, AF, Smith, JA, Kardia, SLR, Hovatta, I, Perola, M, Ripatti, S, Salomaa, V, Henders, AK, Martin, NG, Smith, AK, Mehta, D, Binder, EB, Nylocks, KM, Kennedy, EM, Klengel, T, Ding, J, Suchy-Dicey, AM, Enquobahrie, DA, Brody, J, Rotter, JI, Chen, YDI, Houwing-Duistermaat, J, Kloppenburg, M, Slagboom, PE, Helmer, Q, Den Hollander, W, Bean, S, Raj, T, Bakhshi, N, Wang, QP, Oyston, LJ, Psaty, BM, Tracy, RP, Montgomery, GW, Turner, ST, Blangero, J, Neely, Graham
المصدر: urn:ISSN:2041-1723 ; Nature Communications, 6, 1, 8570
بيانات النشر: Springer Nature
سنة النشر: 2015
المجموعة: UNSW Sydney (The University of New South Wales): UNSWorks
مصطلحات موضوعية: Human Genome, Genetics, Biotechnology, 2 Aetiology, 2.1 Biological and endogenous factors, 1.1 Normal biological development and functioning, 1 Underpinning research, Aging, Biomarkers, DNA Methylation, Gene Expression Profiling, Humans, Transcriptome, White People, NABEC/UKBEC Consortium
الوصف: Disease incidences increase with age, but the molecular characteristics of ageing that lead to increased disease susceptibility remain inadequately understood. Here we perform a whole-blood gene expression meta-analysis in 14,983 individuals of European ancestry (including replication) and identify 1,497 genes that are differentially expressed with chronological age. The age-associated genes do not harbor more age-associated CpG-methylation sites than other genes, but are instead enriched for the presence of potentially functional CpG-methylation sites in enhancer and insulator regions that associate with both chronological age and gene expression levels. We further used the gene expression profiles to calculate the 'transcriptomic age' of an individual, and show that differences between transcriptomic age and chronological age are associated with biological features linked to ageing, such as blood pressure, cholesterol levels, fasting glucose, and body mass index. The transcriptomic prediction model adds biological relevance and complements existing epigenetic prediction models, and can be used by others to calculate transcriptomic age in external cohorts.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
العلاقة: http://hdl.handle.net/1959.4/unsworks_41983Test; https://doi.org/10.1038/ncomms9570Test
DOI: 10.1038/ncomms9570
الإتاحة: https://doi.org/10.1038/ncomms9570Test
http://hdl.handle.net/1959.4/unsworks_41983Test
حقوق: open access ; https://purl.org/coar/access_right/c_abf2Test ; CC BY ; https://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.D5B54E84
قاعدة البيانات: BASE
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[Value] => edsbas.oa ) ) [Titles] => Array ( [0] => Array ( [TitleFull] => urn:ISSN:2041-1723 ; Nature Communications, 6, 1, 8570 [Type] => main ) ) ) ) ) ) )
IllustrationInfo