Evidence map›Paper›PMID 30622246›Full record

ArticleNature communications2019

Central dogma rates and the trade-off between precision and economy in gene expression.

Jean Hausser, Avi Mayo, Leeat Keren, Uri Alon

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

105 citing papers in PubMed.

  1. Review
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  7. Review
  8. Parameter Evolvability in Gene Expression Models Drives Phenotypic Adaptation.ALIFE : proceedings of the artificial life conference. International Conference on Artificial Life · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Review
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  14. Review
  15. Article
  16. Protein overabundance is driven by growth robustness.bioRxiv : the preprint server for biology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Article

45 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Jean HausserDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, 76100, Israel. jean@hausser.org.ORCID http://orcid.org/0000-0002-3321-7199
Avi MayoDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, 76100, Israel.
Leeat KerenDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, 76100, Israel.
Uri AlonDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, 76100, Israel. uri.alon@weizmann.ac.il.

Funding

European Research Council 249919
6 · The paper itself

Abstract

Steady-state protein abundance is set by four rates: transcription, translation, mRNA decay and protein decay. A given protein abundance can be obtained from infinitely many combinations of these rates. This raises the question of whether the natural rates for each gene result from historical accidents, or are there rules that give certain combinations a selective advantage? We address this question using high-throughput measurements in rapidly growing cells from diverse organisms to find that about half of the rate combinations do not exist: genes that combine high transcription with low translation are strongly depleted. This depletion is due to a trade-off between precision and economy: high transcription decreases stochastic fluctuations but increases transcription costs. Our theory quantitatively explains which rate combinations are missing, and predicts the curvature of the fitness function for each gene. It may guide the design of gene circuits with desired expression levels and noise.

Indexed as

Models, GeneticAnimalsComputational BiologyDatasets as TopicEscherichia coliGene Expression RegulationGene Regulatory NetworksGenetic FitnessGenomeHigh-Throughput Screening AssaysHumansMiceProtein BiosynthesisRNA, MessengerRNA StabilitySaccharomyces cerevisiaeRNA, Messenger

Identifiers

PMID30622246
PMCPMC6325141

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.