A Quantitative Proteome Map of the Human Body
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Abstract
SUMMARY Determining protein levels in each tissue and how they compare with RNA levels is important for understanding human biology and disease as well as regulatory processes that control protein levels. We quantified the relative protein levels from over 12,000 genes across 32 normal human tissues. Tissue-specific or tissue-enriched proteins were identified and compared to transcriptome data. Many ubiquitous transcripts are found to encode tissue-specific proteins. Discordance of RNA and protein enrichment revealed potential sites of synthesis and action of secreted proteins. The tissue-specific distribution of proteins also provides an in-depth view of complex biological events that require the interplay of multiple tissues. Most importantly, our study demonstrated that protein tissue-enrichment information can explain phenotypes of genetic diseases, which cannot be obtained by transcript information alone. Overall, our results demonstrate how understanding protein levels can provide insights into regulation, secretome, metabolism, and human diseases.
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mRNA abundance is not always a faithful proxy of protein expression across various organisms.
“Although transcriptomic profiling has provided insights into Tex cell biology, mRNA abundance is not always a faithful proxy of protein expression across various organisms18–22.”
From Proteotoxic stress response drives T cell exhaustion and immune evasion (2025) · cites this paper as [21]
The Introduction says protein levels often correlate poorly with transcript levels, and the Results (Correlation between RNA and Protein Levels) report a median RNA–protein correlation of 0.46 across 32 human tissues. This supports the point that mRNA is not always a faithful proxy for protein expression, but the paper’s own analysis is of human tissues, not various organisms. (LLM, conf=0.84)
Experimental — accuracy not yet measuredCorrelation between the mRNAs for the paired RNA-Seq relative to the global proteomics datasets showed lower positive Pearson correlation values ranging from 0.333 - 0.378 for all genotypes tested.
“Correlation between the mRNAs for the paired RNA-Seq relative to the global proteomics datasets showed lower positive Pearson correlation values ranging from 0.333 – 0.378 for all genotypes tested which is consistent with prior studies on transcriptome / proteome correlation82–84.”
From EXOSC3 G191 Variants Trigger System-Wide Recalibration of RNA Processing Machinery (2026) · cites this paper as [83]
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High-Resolved Near-Field Sensing by Means of Dielectric Grating With a Box-Like Resonance Shape
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Comprehensive Analysis of N6-Methyladenosine (m6A) Writers, Erasers, and Readers in Cervical Cancer
Condic, M., Ralser, D. J., Klümper, N., Ellinger, J., Qureischi, M., EGGER, E. K., Kristiansen, G., Mustea, A., & Thiesler, T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137165 · Cited by 29 · see citing works
- Authors
- Jiang, L., Wang, M., Lin, S., Jian, R., Li, X., Chan, J., Dong, G., Fang, H., Robinson, A. E., Aguet, F., Anand, S., Ardlie, K. G., Gabriel, S., Getz, G., Graubert, A., Hadley, K., Handsaker, R. E., Huang, K. H., Kashin, S., MacArthur, D. G., Meier, S. R., Nedzel, J. L., Nguyen, D. Y., Segrè, A. V., Todres, E., Balliu, B., Barbeira, A. N., Battle, A., Bonazzola, R., Brown, A., Brown, C. D., Castel, S. E., Conrad, D., Cotter, D. J., Cox, N., Das, S., de Goede, O. M., Dermitzakis, E. T., Engelhardt, B. E., Eskin, E., Eulalio, T. Y., Ferraro, N. M., Flynn, E., Fresard, L., Gamazon, E. R., Garrido-Martín, D., Gay, N. R., Guigó, R., Hamel, A. R., He, Y., Hoffman, P. J., Hormozdiari, F., Hou, L., Im, H. K., Jo, B., Kasela, S., Kellis, M., Kim-Hellmuth, S., Kwong, A., Lappalainen, T., Li, X., Liang, Y., Mangul, S., Mohammadi, P., Montgomery, S. B., Muñoz-Aguirre, M., Nachun, D. C., Nobel, A. B., Oliva, M., Park, Y., Park, Y., Parsana, P., Reverter, F., Rouhana, J. M., Sabatti, C., Saha, A., Skol, A. D., Stephens, M., Stranger, B. E., Strober, B. J., Teran, N. A., Viñuela, A., Wang, G., Wen, X., Wright, F., Wucher, V., Zou, Y., Ferreira, P. G., Li, G., Melé, M., Yeger-Lotem, E., Barcus, M. E., Bradbury, D., Krubit, T., McLean, J. A., Qi, L., Robinson, K., Roche, N. V., Smith, A. M., Sobin, L., Tabor, D. E., Undale, A., Bridge, J., Brigham, L. E., Foster, B. A., Gillard, B. M., Hasz, R., Hunter, M., Johns, C., Johnson, M., Karasik, E., Kopen, G., Leinweber, W. F., McDonald, A., Moser, M. T., Myer, K., Ramsey, K. D., Roe, B., Shad, S., Thomas, J. A., Walters, G., Washington, M., Wheeler, J., Jewell, S. D., Rohrer, D. C., Valley, D. R., Davis, D. A., Mash, D. C., Branton, P. A., Barker, L. K., Gardiner, H. M., Mosavel, M., Siminoff, L. A., Flicek, P., Haeussler, M., Juettemann, T., Kent, W. J., Lee, C. M., Powell, C. C., Rosenbloom, K. R., Ruffier, M., Sheppard, D., Taylor, K., Trevanion, S. J., Zerbino, D. R., Abell, N. S., Akey, J., Chen, L., Demanelis, K., Doherty, J. A., Feinberg, A. P., Hansen, K. D., Hickey, P. F., Jasmine, F., Kaul, R., Kibriya, M. G., Li, J. B., Li, Q., Linder, S. E., Pierce, B. L., Rizzardi, L. F., Smith, K. S., Stamatoyannopoulos, J., Tang, H., Carithers, L. J., Guan, P., Koester, S. E., Little, A. R., Moore, H. M., Nierras, C. R., Rao, A. K., Vaught, J. B., Volpi, S., & Snyder, M. P.
- Affiliations
- Stanford Medicine (US)
- University of Washington (US)
- Thermo Fisher Scientific (United States) (US)
- Corresponding author
- Snyder, Michael P.
- ORCID
- Jiang, Lihua
- Wang, Meng
- Lin, Shin
- Jian, Ruiqi
- Li, Xiao
- Chan, Joanne
- Dong, Guanlan
- Fang, Huaying
- Robinson, Aaron E.
- Aguet, François
- Anand, Shankara
- Ardlie, Kristin G.
- Gabriel, Stacey
- Getz, Gad
- Graubert, Aaron
- Hadley, Kane
- Handsaker, Robert E.
- Huang, Katherine H.
- Kashin, Seva
- MacArthur, Daniel G.
- Meier, Samuel R.
- Nedzel, Jared L.
- Segrè, Ayellet V.
- Todres, Ellen
- Balliu, Brunilda
- Barbeira, Alvaro N.
- Battle, Alexis
- Bonazzola, Rodrigo
- Brown, Andrew
- Brown, Christopher D.
- Castel, Stephane E.
- Cotter, Daniel J.
- Cox, Nancy
- Das, Sayantan
- Dermitzakis, Emmanouil T.
- Engelhardt, Barbara E.
- Eskin, Eleazar
- Eulalio, Tiffany Y.
- Ferraro, Nicole M.
- Flynn, Elise
- Gamazon, Eric R.
- Garrido-Martín, Diego
- Gay, Nicole R.
- Guigó, Roderic
- Hamel, Andrew R.
- He, Yuan
- Hormozdiari, Farhad
- Hou, Lei
- Im, Hae Kyung
- Jo, Brian
- Kasela, Silva
- Kellis, Manolis
- Kim-Hellmuth, Sarah
- Kwong, Alan
- Lappalainen, Tuuli
- Li, Xin
- Liang, Yanyu
- Mangul, Serghei
- Mohammadi, Pejman
- Montgomery, Stephen B.
- Muñoz-Aguirre, Manuel
- Nachun, Daniel C.
- Nobel, Andrew B.
- Oliva, Meritxell
- Park, YoSon
- Park, Yongjin
- Parsana, Princy
- Rouhana, John M.
- Sabatti, Chiara
- Saha, Ashis
- Skol, Andrew D.
- Stephens, Matthew
- Stranger, Barbara E.
- Strober, Benjamin J.
- Teran, Nicole A.
- Viñuela, Ana
- Wang, Gao
- Wen, Xiaoquan
- Wright, Fred
- Wucher, Valentin
- Zou, Yuxin
- Ferreira, Pedro G.
- Li, Gen
- Melé, Marta
- Smith, Anna M.
- Tabor, David E.
- Foster, Barbara A.
- Gillard, Bryan M.
- Hasz, Richard
- Johns, Christopher
- Johnson, Mark
- Moser, Michael T.
- Jewell, Scott D.
- Rohrer, Daniel C.
- Davis, David A.
- Mash, Deborah C.
- Branton, Philip A.
- Gardiner, Heather M.
- Mosavel, Maghboeba
- Siminoff, Laura A.
- Flicek, Paul
- Haeussler, Maximilian
- Juettemann, Thomas
- Lee, Christopher M.
- Rosenbloom, Kate R.
- Ruffier, Magali
- Sheppard, Dan
- Taylor, Kieron
- Trevanion, Stephen J.
- Zerbino, Daniel R.
- Abell, Nathan S.
- Akey, Joshua
- Chen, Lin
- Demanelis, Kathryn
- Doherty, Jennifer A.
- Feinberg, Andrew P.
- Hansen, Kasper D.
- Hickey, Peter F.
- Jasmine, Farzana
- Kaul, Rajinder
- Kibriya, Muhammad G.
- Li, Jin Billy
- Li, Qin
- Pierce, Brandon L.
- Rizzardi, Lindsay F.
- Smith, Kevin S.
- Stamatoyannopoulos, John
- Tang, Hua
- Guan, Ping
- Little, A. Roger
- Moore, Helen M.
- Volpi, Simona
- Snyder, Michael P.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2020-10
- Volume
- 183
- Issue
- 1
- Pages
- 269-283.e19
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC7575058
- OpenAlex
- W3083820674
- Semantic Scholar
- 433ccfe1fc4a69e669d65b7624ab4341f13fa1a9
- Cited by
- 458
- References
- 72
- Citations by year
- 2026: 56 · 2025: 105 · 2024: 83 · 2023: 96 · 2022: 61 · 2021: 46 · 2020: 10 · 2019: 1
- FWCI
- 20.43
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Discovery Research Portal (University of Dundee) (submittedVersion)
- Funders
- National Institutes of Health
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced Biosensing Techniques and Applications
- Keywords
- human proteome, tissue-specific proteins, protein abundance, transcriptome, RNA-protein correlation, secretome
- MeSH terms
- Humans, RNA, RNA, Messenger, Gene Expression, Proteome, Gene Expression Profiling, Proteomics, Transcriptome
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