Academic Journal

Global molecular changes in rat livers treated with RXR agonists: a comparison using transcriptomics and proteomics

التفاصيل البيبلوغرافية
العنوان: Global molecular changes in rat livers treated with RXR agonists: a comparison using transcriptomics and proteomics
المؤلفون: Vedell, Peter T., Townsend, Reid R., You, Ming, Malone, James P., Grubbs, Clinton J., Bland, Kirby I., Muccio, Donald D., Atigadda, Venkatram R., Chen, Yang, Vignola, Katie, Lubet, Ronald A.
المساهمون: National Center for Research Resources, National Institutes of Health, NIH Roadmap for Medical Research, National Cancer Institute
المصدر: Pharmacology Research & Perspectives ; volume 2, issue 6 ; ISSN 2052-1707 2052-1707
بيانات النشر: Wiley
سنة النشر: 2014
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: The ability of the retinoid X receptors ( RXR s) specific agonists (targretin [ TRG ] and UAB 30) to alter rat liver gene and protein expression was determined using Affymetrix Exon arrays and high‐performance liquid chromatography – tandem mass spectrometry ( LC ‐ MS / MS ). TRG profoundly increases triglycerides levels while UAB 30 does not. The expression patterns of transcripts or proteins from rat liver treated with TRG or UAB ‐30 were different from controls and each other. There were six times more gene transcripts identified than proteins. Differentially expressed RNA s or proteins were mapped into known gene ontology ( GO ) categories and GeneGo Metacore ( KEGG ) pathway maps. The GO categories which were highly overrepresented with differentially expressed RNA s ( P < 10 −16 ) were also overrepresented at the protein level. This high concordance of G O Terms was achieved despite the fact that typically ≤1/3 of the elements identified by gene expression were identified by proteomics. Within these GO categories, the magnitude of alterations induced by RXR agonists at the transcript and protein levels were correlated. When GO categories with moderate overrepresentation (10 −5 < P < 10 −9 ) were examined, there was greater discordance between the transcript and protein data. Examination of KEGG pathway maps with highly significant changes at both the protein and the RNA levels showed that the individual proteins/genes altered were often the same and changes were of similar magnitude; while KEGG pathways showed limited statistical significance and exhibited minimal overlap. Finally, metabolomics analysis of liver and serum identified altered expression of metabolites related to fatty acid oxidation and bile acid metabolism that were consistent with transcript/protein changes. We observed significant concordance between genomics and proteomics implying either can identify pathways modulated and can indirectly predict resulting physiologic effects.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/prp2.74
الاتاحة: http://dx.doi.org/10.1002/prp2.74
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fprp2.74
https://onlinelibrary.wiley.com/doi/pdf/10.1002/prp2.74
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/prp2.74
https://bpspubs.onlinelibrary.wiley.com/doi/pdf/10.1002/prp2.74
Rights: http://creativecommons.org/licenses/by-nc-nd/3.0/
رقم الانضمام: edsbas.2AD78CAB
قاعدة البيانات: BASE