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Proteogenomic analysis of psoriasis reveals discordant and concordant changes in mRNA and protein abundance

dc.contributor.authorSwindell, William R
dc.contributor.authorRemmer, Henriette A
dc.contributor.authorSarkar, Mrinal K
dc.contributor.authorXing, Xianying
dc.contributor.authorBarnes, Drew H
dc.contributor.authorWolterink, Liza
dc.contributor.authorVoorhees, John J
dc.contributor.authorNair, Rajan P
dc.contributor.authorJohnston, Andrew
dc.contributor.authorElder, James T
dc.contributor.authorGudjonsson, Johann E
dc.date.accessioned2015-08-06T18:02:29Z
dc.date.available2015-08-06T18:02:29Z
dc.date.issued2015-08-04
dc.identifier.citationGenome Medicine. 2015 Aug 04;7(1):86
dc.identifier.urihttps://hdl.handle.net/2027.42/112309en_US
dc.description.abstractAbstract Background Psoriasis is a chronic disease characterized by the development of scaly red skin lesions and possible co-morbid conditions. The psoriasis lesional skin transcriptome has been extensively investigated, but mRNA levels do not necessarily reflect protein abundance. The purpose of this study was therefore to compare differential expression patterns of mRNA and protein in psoriasis lesions. Methods Lesional (PP) and uninvolved (PN) skin samples from 14 patients were analyzed using high-throughput complementary DNA sequencing (RNA-seq) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). Results We identified 4122 differentially expressed genes (DEGs) along with 748 differentially expressed proteins (DEPs). Global shifts in mRNA were modestly correlated with changes in protein abundance (r = 0.40). We identified similar numbers of increased and decreased DEGs, but 4-fold more increased than decreased DEPs. Ribosomal subunit and translation proteins were elevated within lesions, without a corresponding shift in mRNA expression (RPL3, RPS8, RPL11). We identified 209 differentially expressed genes/proteins (DEGPs) with corresponding trends at the transcriptome and proteome levels. Most DEGPs were similarly altered in at least one other skin disease. Psoriasis-specific and non-specific DEGPs had distinct cytokine-response patterns, with only the former showing disproportionate induction by IL-17A in cultured keratinocytes. Conclusions Our findings reveal global imbalance between the number of increased and decreased proteins in psoriasis lesions, consistent with heightened translation. This effect could not have been discerned from mRNA profiling data alone. High-confidence DEGPs were identified through transcriptome-proteome integration. By distinguishing between psoriasis-specific and non-specific DEGPs, our analysis uncovered new functional insights that would otherwise have been overlooked.
dc.titleProteogenomic analysis of psoriasis reveals discordant and concordant changes in mRNA and protein abundance
dc.typeArticleen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/112309/1/13073_2015_Article_208.pdf
dc.identifier.doi10.1186/s13073-015-0208-5en_US
dc.language.rfc3066en
dc.rights.holderSwindell et al.
dc.date.updated2015-08-06T18:02:32Z
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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