- Open Access
Fitness-Driven Scaling Laws between mRNA and Protein Levels
Phys. Rev. Lett. 137, 048402 – Published 22 July, 2026
DOI: https://doi.org/10.1103/gkzp-r681
Abstract
The relationship between protein and messenger RNA (mRNA) levels is a key aspect of gene expression. Although a strong mRNA-protein correlation is widely observed, the evolutionary force driving the correlation remains poorly understood, undermining the reliability of using mRNA abundance as a proxy for protein levels. Here, by balancing the cost and benefit of gene expression, we uncover an optimal scaling between mRNA () and protein () levels that maximizes cell fitness: . Notably, we predict a lower bound of 0.5 for the exponent, and the toxicity effects of protein overexpression further increase it. For the model organism Saccharomyces cerevisiae, the simulated scaling across the genome, incorporating biologically relevant parameters, aligns well with experimental data. Genome-wide data across multiple organisms all exhibit a scaling exponent above the predicted lower bound. Our Letter rationalizes the primary role of transcriptional regulation and also the significance of translational regulation in determining protein levels from an evolutionary perspective.
Physics Subject Headings (PhySH)
Article Text
Supplemental Material
References (98)
- A. Wagner, Energy constraints on the evolution of gene expression, Mol. Biol. Evol. 22, 1365 (2005).
- E. Dekel and U. Alon, Optimality and evolutionary tuning of the expression level of a protein, Nature (London) 436, 588 (2005).
- M. Kafri, E. Metzl-Raz, G. Jona, and N. Barkai, The cost of protein production, Cell Rep. 14, 22 (2016).
- J. M. Peters, A. Colavin, H. Shi, T. L. Czarny, M. H. Larson, S. Wong, J. S. Hawkins, C. H. Lu, B.-M. Koo, E. Marta et al., A comprehensive, crispr-based functional analysis of essential genes in bacteria, Cell 165, 1493 (2016).
- T. W. Lo, H. J. Choi, D. Huang, and P. A. Wiggins, Noise robustness and metabolic load determine the principles of central dogma regulation, Sci. Adv. 10, eado3095 (2024).
- N. M. Belliveau, G. Chure, C. L. Hueschen, H. G. Garcia, J. Kondev, D. S. Fisher, J. A. Theriot, and R. Phillips, Fundamental limits on the rate of bacterial growth and their influence on proteomic composition, Cell Syst. 12, 924 (2021).
- J. Paulsson, Summing up the noise in gene networks, Nature (London) 427, 415 (2004).
- J. M. Raser and E. K. O’shea, Noise in gene expression: Origins, consequences, and control, Science 309, 2010 (2005).
- J. R. Newman, S. Ghaemmaghami, J. Ihmels, D. K. Breslow, M. Noble, J. L. DeRisi, and J. S. Weissman, Single-cell proteomic analysis of S. cerevisiae reveals the architecture of biological noise, Nature (London) 441, 840 (2006).
- A. Sanchez, S. Choubey, and J. Kondev, Regulation of noise in gene expression, Annu. Rev. Biophys. 42, 469 (2013).
- J. Lin and A. Amir, The effects of stochasticity at the single-cell level and cell size control on the population growth, Cell Syst. 5, 358 (2017).
- W. E. Bentley, N. Mirjalili, D. C. Andersen, R. H. Davis, and D. S. Kompala, Plasmid-encoded protein: The principal factor in the metabolic burden associated with recombinant bacteria, Biotechnol. Bioeng. 35, 668 (1990).
- H. Dong, L. Nilsson, and C. G. Kurland, Gratuitous overexpression of genes in escherichia coli leads to growth inhibition and ribosome destruction, J. Bacteriol. 177, 1497 (1995).
- C. Rang, J. E. Galen, J. B. Kaper, and L. Chao, Fitness cost of the green fluorescent protein in gastrointestinal bacteria, Can. J. Microbiol. 49, 531 (2003).
- M. Scott, C. W. Gunderson, E. M. Mateescu, Z. Zhang, and T. Hwa, Interdependence of cell growth and gene expression: Origins and consequences, Science 330, 1099 (2010).
- M. Lynch and G. K. Marinov, The bioenergetic costs of a gene, Proc. Natl. Acad. Sci. U.S.A. 112, 15690 (2015).
- A. San Millan, M. Toll-Riera, Q. Qi, and R. C. MacLean, Interactions between horizontally acquired genes create a fitness cost in pseudomonas aeruginosa, Nat. Commun. 6, 6845 (2015).
- Y. Eguchi, K. Makanae, T. Hasunuma, Y. Ishibashi, K. Kito, and H. Moriya, Estimating the protein burden limit of yeast cells by measuring the expression limits of glycolytic proteins, eLife 7, e34595 (2018).
- L. Keren, J. Hausser, M. Lotan-Pompan, I. V. Slutskin, H. Alisar, S. Kaminski, A. Weinberger, U. Alon, R. Milo, and E. Segal, Massively parallel interrogation of the effects of gene expression levels on fitness, Cell 166, 1282 (2016).
- J. S. Rest, C. M. Morales, J. B. Waldron, D. A. Opulente, J. Fisher, S. Moon, K. Bullaughey, L. B. Carey, and D. Dedousis, Nonlinear fitness consequences of variation in expression level of a eukaryotic gene, Mol. Biol. Evol. 30, 448 (2012).
- F. Duveau, W. Toubiana, and P. J. Wittkopp, Fitness effects of cis-regulatory variants in the Saccharomyces cerevisiae TDH3 promoter, Mol. Biol. Evol. 34, 2908 (2017).
- F. Duveau, A. Hodgins-Davis, B. P. Metzger, B. Yang, S. Tryban, E. A. Walker, T. Lybrook, and P. J. Wittkopp, Fitness effects of altering gene expression noise in Saccharomyces cerevisiae, eLife 7, e37272 (2018).
- F. Duveau, P. Vande Zande, B. P. Metzger, C. J. Diaz, E. A. Walker, S. Tryban, M. A. Siddiq, B. Yang, and P. J. Wittkopp, Mutational sources of trans-regulatory variation affecting gene expression in Saccharomyces cerevisiae, eLife 10, e67806 (2021).
- G. I. Lang, A. W. Murray, and D. Botstein, The cost of gene expression underlies a fitness trade-off in yeast, Proc. Natl. Acad. Sci. U.S.A. 106, 5755 (2009).
- F. J. Poelwijk, P. D. Heyning, M. G. de Vos, D. J. Kiviet, and S. J. Tans, Optimality and evolution of transcriptionally regulated gene expression, BMC Syst. Biol. 5, 128 (2011).
- A. Y. Weiße, D. A. Oyarzún, V. Danos, and P. S. Swain, Mechanistic links between cellular trade-offs, gene expression, and growth, Proc. Natl. Acad. Sci. U.S.A. 112, E1038 (2015).
- P. Vande Zande, M. S. Hill, and P. J. Wittkopp, Pleiotropic effects of trans-regulatory mutations on fitness and gene expression, Science 377, 105 (2022).
- A. Gyorgy, Competition and evolutionary selection among core regulatory motifs in gene expression control, Nat. Commun. 14, 8266 (2023).
- D. E. Weinberg, P. Shah, S. W. Eichhorn, J. A. Hussmann, J. B. Plotkin, and D. P. Bartel, Improved ribosome-footprint and mRNA measurements provide insights into dynamics and regulation of yeast translation, Cell Rep. 14, 1787 (2016).
- R. Balakrishnan, M. Mori, I. Segota, Z. Zhang, R. Aebersold, C. Ludwig, and T. Hwa, Principles of gene regulation quantitatively connect DNA to RNA and proteins in bacteria, Science 378, eabk2066 (2022).
- S. Marguerat, A. Schmidt, S. Codlin, W. Chen, R. Aebersold, and J. Bähler, Quantitative analysis of fission yeast transcriptomes and proteomes in proliferating and quiescent cells, Cell 151, 671 (2012).
- S. W. Eichhorn, H. Guo, S. E. McGeary, R. A. Rodriguez-Mias, C. Shin, D. Baek, S.-h. Hsu, K. Ghoshal, J. Villén, and D. P. Bartel, mRNA destabilization is the dominant effect of mammalian micrornas by the time substantial repression ensues, Mol. Cell 56, 104 (2014).
- J. J. Li, P. J. Bickel, and M. D. Biggin, System wide analyses have underestimated protein abundances and the importance of transcription in mammals, PeerJ 2, e270 (2014).
- J. J. Li and M. D. Biggin, Statistics requantitates the central dogma, Science 347, 1066 (2015).
- Y. Liu, A. Beyer, and R. Aebersold, On the dependency of cellular protein levels on mRNA abundance, Cell 165, 535 (2016).
- C. Buccitelli and M. Selbach, mRNAs, proteins and the emerging principles of gene expression control, Nat. Rev. Genet. 21, 630 (2020).
- C. Vogel, R. de Sousa Abreu, D. Ko, S.-Y. Le, B. A. Shapiro, S. C. Burns, D. Sandhu, D. R. Boutz, E. M. Marcotte, and L. O. Penalva, Sequence signatures and mRNA concentration can explain two-thirds of protein abundance variation in a human cell line, Mol. Syst. Biol. 6, 400 (2010).
- G. Csárdi, A. Franks, D. S. Choi, E. M. Airoldi, and D. A. Drummond, Accounting for experimental noise reveals that MRNA levels, amplified by post-transcriptional processes, largely determine steady-state protein levels in yeast, PLoS Genet. 11, e1005206 (2015).
- B. Ho, A. Baryshnikova, and G. W. Brown, Unification of protein abundance datasets yields a quantitative Saccharomyces cerevisiae proteome, Cell Syst. 6, 192 (2018).
- See Supplemental Material http://link.aps.org/supplemental/10.1103/gkzp-r681 for more details on the fitness functions, numerical simulations, and statistics of all datasets used, which also includes Refs. [41–73].
- T. Kalisky, E. Dekel, and U. Alon, Cost–benefit theory and optimal design of gene regulation functions, Phys. Biol. 4, 229 (2007).
- R. Milo and R. Phillips, Cell Biology by the Numbers (Garland Science, New York, NY, USA, 2015).
- P. Eser, C. Demel, K. C. Maier, B. Schwalb, N. Pirkl, D. E. Martin, P. Cramer, and A. Tresch, Periodic mRNA synthesis and degradation co-operate during cell cycle gene expression, Mol. Syst. Biol. 10, 717 (2014).
- B. Neymotin, R. Athanasiadou, and D. Gresham, Determination of in vivo RNA kinetics using RATE-seq, RNA 20, 1645 (2014).
- C. Miller, B. Schwalb, K. Maier, D. Schulz, S. Dümcke, B. Zacher, A. Mayer, J. Sydow, L. Marcinowski, L. Dölken et al., Dynamic transcriptome analysis measures rates of mRNA synthesis and decay in yeast, Mol. Syst. Biol. 7, 458 (2011).
- R. Christiano, N. Nagaraj, F. Fröhlich, and T. C. Walther, Global proteome turnover analyses of the yeasts S. cerevisiae and S. pombe, Cell Rep. 9, 1959 (2014).
- M. Martin-Perez and J. Villén, Determinants and regulation of protein turnover in yeast, Cell Syst. 5, 283 (2017).
- R. Christiano, H. Arlt, S. Kabatnik, N. Mejhert, Z. W. Lai, R. V. Farese, and T. C. Walther, A systematic protein turnover map for decoding protein degradation, Cell Rep. 33, 108378 (2020).
- J. M. Pratt, J. Petty, I. Riba-Garcia, D. H. Robertson, S. J. Gaskell, S. G. Oliver, and R. J. Beynon, Dynamics of protein turnover, a missing dimension in proteomics, Mol. Cell. Proteomics 1, 579 (2002).
- F. Miura, N. Kawaguchi, M. Yoshida, C. Uematsu, K. Kito, Y. Sakaki, and T. Ito, Absolute quantification of the budding yeast transcriptome by means of competitive PCR between genomic and complementary DNAs, BMC Genomics 9, 574 (2008).
- H. F. Lodish, A. Berk, C. Kaiser, M. Krieger, A. Bretscher, H. L. Ploegh, K. C. Martin, M. B. Yaffe, and A. Amon, Molecular Cell Biology (Macmillan, New York, 2021).
- D. A. Drummond, J. D. Bloom, C. Adami, C. O. Wilke, and F. H. Arnold, Why highly expressed proteins evolve slowly, Proc. Natl. Acad. Sci. U.S.A. 102, 14338 (2005).
- M. Oeffinger and D. Zenklusen, To the pore and through the pore: A story of mRNA export kinetics, Biochim. Biophys. Acta (BBA)-Gene Regul. Mech. 1819, 494 (2012).
- U. Raue, S. Oellerer, and S. Rospert, Association of protein biogenesis factors at the yeast ribosomal tunnel exit is affected by the translational status and nascent polypeptide sequence, J. Biol. Chem. 282, 7809 (2007).
- E. M. Phizicky and A. K. Hopper, tRNA biology charges to the front, Genes Dev. 24, 1832 (2010).
- E. Metzl-Raz, M. Kafri, G. Yaakov, I. Soifer, Y. Gurvich, and N. Barkai, Principles of cellular resource allocation revealed by condition-dependent proteome profiling, eLife 6, e28034 (2017).
- T. Borggrefe, R. Davis, A. Bareket-Samish, and R. D. Kornberg, Quantitation of the RNA polymerase II transcription machinery in yeast, J. Biol. Chem. 276, 47150 (2001).
- A. Riba, N. Di Nanni, N. Mittal, E. Arhné, A. Schmidt, and M. Zavolan, Protein synthesis rates and ribosome occupancies reveal determinants of translation elongation rates, Proc. Natl. Acad. Sci. U.S.A. 116, 15023 (2019).
- T. von der Haar, A quantitative estimation of the global translational activity in logarithmically growing yeast cells, BMC Syst. Biol. 2, 87 (2008).
- A. M. Edwards, C. M. Kane, R. A. Young, and R. D. Kornberg, Two dissociable subunits of yeast RNA polymerase II stimulate the initiation of transcription at a promoter in vitro, J. Biol. Chem. 266, 71 (1991).
- D. R. Larson, D. Zenklusen, B. Wu, J. A. Chao, and R. H. Singer, Real-time observation of transcription initiation and elongation on an endogenous yeast gene, Science 332, 475 (2011).
- V. Pelechano, S. Chavez, and J. E. Perez-Ortin, A complete set of nascent transcription rates for yeast genes, PLoS One 5, e15442 (2010).
- B. Futcher, G. Latter, P. Monardo, C. McLaughlin, and J. Garrels, A sampling of the yeast proteome, Mol. Cell. Biol. 19, 7357 (1999).
- S. Islam, A. Zeisel, S. Joost, G. La Manno, P. Zajac, M. Kasper, P. Lönnerberg, and S. Linnarsson, Quantitative single-cell RNA-seq with unique molecular identifiers, Nat. Methods 11, 163 (2014).
- I. Jarmoskaite, S. K. Denny, P. P. Vaidyanathan, W. R. Becker, J. O. Andreasson, C. J. Layton, K. Kappel, V. Shivashankar, R. Sreenivasan, R. Das et al., A quantitative and predictive model for RNA binding by human pumilio proteins, Mol. Cell 74, 966 (2019).
- G. V. Dolgalev, T. A. Safonov, V. A. Arzumanian, O. I. Kiseleva, and E. V. Poverennaya, Estimating total quantitative protein content in escherichia coli, saccharomyces cerevisiae, and hela cells, Int. J. Mol. Sci. 24, 2081 (2023).
- J. W. Posakony, J. M. England, and G. Attardi, Mitochondrial growth and division during the cell cycle in hela cells, J. Cell Biol. 74, 468 (1977).
- S. B. Cambridge, F. Gnad, C. Nguyen, J. L. Bermejo, M. Kruger, and M. Mann, Systems-wide proteomic analysis in mammalian cells reveals conserved, functional protein turnover, J. Proteome Res. 10, 5275 (2011).
- M. Jovanovic, M. S. Rooney, P. Mertins, D. Przybylski, N. Chevrier, R. Satija, E. H. Rodriguez, A. P. Fields, S. Schwartz, R. Raychowdhury et al., Dynamic profiling of the protein life cycle in response to pathogens, Science 347, 1259038 (2015).
- R. C. Jansen, J.-P. Nap, and L. Mlynárová, Errors in genomics and proteomics, Nat. Biotechnol. 20, 19 (2002).
- G. H. Golub and C. F. Van Loan, An analysis of the total least squares problem, SIAM J. Numer. Anal. 17, 883 (1980).
- I. Markovsky and S. Van Huffel, Overview of total least-squares methods, Signal Processing 87, 2283 (2007).
- N. Draper, Applied Regression Analysis (McGraw-Hill. Inc, New York, 1998).
- P. Shah, Y. Ding, M. Niemczyk, G. Kudla, and J. B. Plotkin, Rate-limiting steps in yeast protein translation, Cell 153, 1589 (2013).
- F. Ceroni, R. Algar, G.-B. Stan, and T. Ellis, Quantifying cellular capacity identifies gene expression designs with reduced burden, Nat. Methods 12, 415 (2015).
- G. Wu, Q. Yan, J. A. Jones, Y. J. Tang, S. S. Fong, and M. A. Koffas, Metabolic burden: Cornerstones in synthetic biology and metabolic engineering applications, Trends Biotechnol. 34, 652 (2016).
- J. Lin and A. Amir, Homeostasis of protein and mRNA concentrations in growing cells, Nat. Commun. 9, 4496 (2018).
- Y. Han and F. Zhang, Control strategies to manage trade-offs during microbial production, Curr. Opin. Biotechnol. 66, 158 (2020).
- Q. Wang and J. Lin, Heterogeneous recruitment abilities to RNA polymerases generate nonlinear scaling of gene expression with cell volume, Nat. Commun. 12, 6852 (2021).
- M. P. Swaffer, G. K. Marinov, H. Zheng, L. F. Valenzuela, C. Y. Tsui, A. W. Jones, J. Greenwood, A. Kundaje, W. J. Greenleaf, R. Reyes-Lamothe et al., RNA polymerase II dynamics and mRNA stability feedback scale mRNA amounts with cell size, Cell 186, 5254 (2023).
- L. Calabrese, L. Ciandrini, and M. Cosentino Lagomarsino, How total mRNA influences cell growth, Proc. Natl. Acad. Sci. U.S.A. 121, e2400679121 (2024).
- D. M. Stoebel, A. M. Dean, and D. E. Dykhuizen, The cost of expression of escherichia coli lac operon proteins is in the process, not in the products, Genetics 178, 1653 (2008).
- I. Frumkin, D. Schirman, A. Rotman, F. Li, L. Zahavi, E. Mordret, O. Asraf, S. Wu, S. F. Levy, and Y. Pilpel, Gene architectures that minimize cost of gene expression, Mol. Cell 65, 142 (2017).
- Y. Yan and J. Lin, Disentangling the fitness cost of gene expression, bioRxiv (2025).
- J. Paulsson, Models of stochastic gene expression, Phys. Life Rev. 2, 157 (2005).
- Y. Taniguchi, P. J. Choi, G.-W. Li, H. Chen, M. Babu, J. Hearn, A. Emili, and X. S. Xie, Quantifying E. coli proteome and transcriptome with single-molecule sensitivity in single cells, Science 329, 533 (2010).
- A. Bar-Even, J. Paulsson, N. Maheshri, M. Carmi, E. O’Shea, Y. Pilpel, and N. Barkai, Noise in protein expression scales with natural protein abundance, Nat. Genet. 38, 636 (2006).
- V. Shahrezaei and P. S. Swain, Analytical distributions for stochastic gene expression, Proc. Natl. Acad. Sci. U.S.A. 105, 17256 (2008).
- M. Mundt, A. Anders, S. M. Murray, and V. Sourjik, A system for gene expression noise control in yeast, ACS Synth. Biol. 7, 2618 (2018).
- N. Friedman, L. Cai, and X. S. Xie, Linking stochastic dynamics to population distribution: An analytical framework of gene expression, Phys. Rev. Lett. 97, 168302 (2006).
- G.-W. Li, D. Burkhardt, C. Gross, and J. S. Weissman, Quantifying absolute protein synthesis rates reveals principles underlying allocation of cellular resources, Cell 157, 624 (2014).
- F. W. Albert, D. Muzzey, J. S. Weissman, and L. Kruglyak, Genetic influences on translation in yeast, PLoS Genet. 10, e1004692 (2014).
- B. Schwanhäusser, D. Busse, N. Li, G. Dittmar, J. Schuchhardt, J. Wolf, W. Chen, and M. Selbach, Global quantification of mammalian gene expression control, Nature (London) 473, 337 (2011).
- N. Nagaraj, J. R. Wisniewski, T. Geiger, J. Cox, M. Kircher, J. Kelso, S. Pääbo, and M. Mann, Deep proteome and transcriptome mapping of a human cancer cell line, Mol. Syst. Biol. 7, 548 (2011).
- F. Edfors, F. Danielsson, B. M. Hallström, L. Käll, E. Lundberg, F. Pontén, B. Forsström, and M. Uhlén, Gene-specific correlation of RNA and protein levels in human cells and tissues, Mol. Syst. Biol. 12, 883 (2016).
- A. Franks, E. Airoldi, and N. Slavov, Post-transcriptional regulation across human tissues, PLoS Comput. Biol. 13, e1005535 (2017).
- L. Bintu, N. E. Buchler, H. G. Garcia, U. Gerland, T. Hwa, J. Kondev, and R. Phillips, Transcriptional regulation by the numbers: Models, Curr. Opin. Genet. Dev. 15, 116 (2005).
- J. Hausser, A. Mayo, L. Keren, and U. Alon, Central dogma rates and the trade-off between precision and economy in gene expression, Nat. Commun. 10, 68 (2019).