Age-dependent regulation of tumor-related microRNAs in the brain of the annual fish Nothobranchius furzeri

被引:40
作者
Baumgart, Mario [2 ]
Groth, Marco [2 ]
Priebe, Steffen [3 ]
Appelt, Jessika [2 ]
Guthke, Reinhard [3 ]
Platzer, Matthias [2 ]
Cellerino, Alessandro [1 ]
机构
[1] CNR, Ist Biofis, Biol Lab, Scuola Normale Super, I-56124 Pisa, Italy
[2] Fritz Lipmann Inst, Leibniz Inst Age Res, Jena, Germany
[3] Leibniz Inst, Hans Knoll Inst Nat Prod Res & Infect Biol, Jena, Germany
关键词
Longevity regulation; Molecular biology of aging; Neuroscience; Central nervous system; Gene expression; MIR-17-92; CLUSTER; VERTEBRATE MODEL; LIFE-SPAN; EXPRESSION; LIVER; RNA; MIR-34A; MIR-29; GENES;
D O I
10.1016/j.mad.2012.03.015
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
MicroRNAs are regulators of gene expression. We used miRNA-seq by the Illumina platform to quantify and compare the temporal miRNA expression profiles in the brain of a short-lived (GRZ) and a longer-lived strain (MZM) of the annual fish Nothobranchius furzeri. We used fuzzy-c-means clustering to group miRNAs with similar profiles. In MZM, we found tumor suppressors with known negative interactions with MYC and/or positive interactions with TP53 among up-regulated miRNAs (e.g. miR-23a, miR-26a/b, miR-29a/b and miR-101a) in aged animals. Conversely, we found oncogenes which are MYC targets among down-regulated miRNAs (miR-7a, members of miR cluster 17 similar to 92). These latter were previously shown to be regulated in human replicative aging. In addition, three regulated miRNAs (miR-181c, miR-29a and miR-338) are known to be age-regulated and to globally contribute to regulation of their targets in the human brain. Therefore, there appears to be a degree of evolutionarily conservation in age-dependent miRNA expression between humans and N. furzeri. GRZ showed specific regulation of some miRNAs, notably a marked up-regulation of miR-124, a miRNA important for neuronal differentiation. The two strains differ in their miRNA expression profiles already at sexual maturity. Short lifespan in GRZ could therefore be - at least partially - due to dysregulated miRNA expression. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:226 / 233
页数:8
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