Proteomics

Dataset Information

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Multi-Omics Analyses Revealed Conserved Aging Signatures in Mice


ABSTRACT: Studies on aging have largely included one or two OMICS layers, which may not necessarily reflect the signatures of other layers. Moreover, most aging studies have often compared very young (4-5 wks) mice with old (24 months) mice which does not reflect the aging transition after the attainment of adulthood. Therefore, we aimed to study and compared muti-OMICS aging signatures across key metabolic tissues of mature adults (6 months) and old (24 months) C57BL/6J mice (the most commonly used mouse strain). Here we compared the differentially regulated genes and enriched pathways for transcriptome, proteome and epigenome (H3K27ac, H3K4me3, H3K27me3, DNA methylation) across liver, heart, and quadriceps muscle. The major aging associated pathways cross multiple layers and tissues are decreased RNA metabolism, transcription, and translation at transcript and protein levels however increased potential of transcription at DNA methylation and H3K27ac levels.

INSTRUMENT(S): TripleTOF 5600

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Quadriceps, Heart, Liver, Gastrocnemius

SUBMITTER: Evan Williams  

LAB HEAD: Ruedi Aebersold

PROVIDER: PXD011142 | Pride | 2021-11-30

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
E1608021307_feature_alignment_requant.tsv.gz Tabular
E1608021307_matrix.xlsx Xlsx
MultiTissueLibrary_LiverSkeletalMuscleHeartBATWholeBrain.TraML Other
YWU_BXD_E1508071446.pep.xml Pepxml
YWU_BXD_E1508071446.prot.xml Xml
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