Kidney mRNA-protein expression correlation: what can we learn from the Human Protein Atlas?

被引:0
作者
Acoba, Dianne [1 ,2 ]
Reznichenko, Anna [1 ]
机构
[1] AstraZeneca, Clin Renal Late Stage Dev Cardiovasc Renal & Metab, BioPharmaceut R&D, Gothenburg, Sweden
[2] Univ Paris Cite, Inst Necker Enfants Malad INEM, Inst Natl Sante & Rech Med INSERM U1151, Paris, France
关键词
Human Protein Atlas; Immunohistochemistry; RNA-seq; Kidney;
D O I
10.1007/s40620-024-02126-z
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
BackgroundThe Human Protein Atlas, with more than 10 million immunohistochemical images showing tissue- and cell-specific protein expression levels and subcellular localization information, is widely used in kidney research. The Human Protein Atlas contains comprehensive data on multi-tissue transcript and protein abundance, allowing for comparisons across tissues. However, while visual and intuitive to interpret, immunohistochemistry is limited by its semi-quantitative nature. This can lead to mismatches in protein expression measurements across different platforms.MethodsWe performed a comparison of the Human Protein Atlas' kidney-specific RNA sequencing and immunohistochemistry data to determine whether the mRNA and protein abundance levels are concordant.ResultsOur study shows that there is a discordance between mRNA and protein expression in the kidney based on the Human Protein Atlas data. Using an external validation mass spectrometry dataset, we show that more than 500 proteins undetected by immunohistochemistry are robustly measured by mass spectrometry. The Human Protein Atlas transcriptome data, on the other hand, exhibit similar transcript detection levels as other kidney RNA-seq datasets.ConclusionsDiscordance in mRNA-protein expression could be due to both biological and technical reasons, such as transcriptional dynamics, translation rates, protein half-lives, and measurement errors. This is further complicated by the heterogeneity of the kidney tissue itself, which can increase the discordance if the cell populations or tissue compartment samples do not match. As such, shedding light on the mRNA-protein relationship of the kidney-specific Human Protein Atlas data can provide context to our scientific inferences on renal gene and protein quantification.
引用
收藏
页码:135 / 141
页数:7
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