Evidence map›Paper›PMID 31084583›Full record

ReviewAnnual review of biophysics2019

Figure 1 Theory Meets Figure 2 Experiments in the Study of Gene Expression.

Rob Phillips, Nathan M Belliveau, Griffin Chure, Hernan G Garcia, Manuel Razo-Mejia, Clarissa Scholes

Abstract readReview
In one paragraph

Review in Annual review of biophysics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Review
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  9. Seeing with an extra sense.Current biology : CB · 2024
    Article
  10. Article
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  15. Article
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  17. A synthetic synthesis to explore animal evolution and development.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  18. Article
  19. Article
  20. Systematic dissection of σCell reports · 2021
    Article
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

6 authors.

Rob PhillipsDepartment of Physics, California Institute of Technology, Pasadena, California, USA; email: phillips@pboc.caltech.edu.
Nathan M BelliveauHoward Hughes Medical Institute, Chevy Chase, Maryland 20815, USA.
Griffin ChureDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, USA.
Hernan G GarciaDepartment of Molecular & Cell Biology, Department of Physics, Biophysics Graduate Group, and Institute for Quantitative Biosciences-QB3, University of California, Berkeley, California, USA.
Manuel Razo-MejiaDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, USA.
Clarissa ScholesDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts, USA.

Funding

The Principles of Regulatory, Conformational and Evolutionary AdaptationR35GM118043 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ROB PHILLIPS · 2016 to 2026
$7.9M
NIH Director's Pioneer Award (RMI)DP1OD000217 · OD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI PHILLIPS, ROB · 2004 to 2008
$4.0M
Single-Molecule and Single-Cell Analysis of Transcription Factor-DNA ComplexesR01GM085286 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI PHILLIPS, ROB · 2009 to 2015
$2.8M
Lighting Up the Central Dogma in Embryonic DevelopmentDP2HD094655 · NICHD · UNIVERSITY OF CALIFORNIA BERKELEY · PI GARCIA, HERNAN GUSTAVO · 2017 to 2017
$2.4M
NICHD NIH HHS DP2 HD094655NIGMS NIH HHS R01 GM085286NIGMS NIH HHS R35 GM118043NIH HHS DP1 OD000217
6 · The paper itself

Abstract

It is tempting to believe that we now own the genome. The ability to read and rewrite it at will has ushered in a stunning period in the history of science. Nonetheless, there is an Achilles' heel exposed by all of the genomic data that has accrued: We still do not know how to interpret them. Many genes are subject to sophisticated programs of transcriptional regulation, mediated by DNA sequences that harbor binding sites for transcription factors, which can up- or down-regulate gene expression depending upon environmental conditions. This gives rise to an input-output function describing how the level of expression depends upon the parameters of the regulated gene-for instance, on the number and type of binding sites in its regulatory sequence. In recent years, the ability to make precision measurements of expression, coupled with the ability to make increasingly sophisticated theoretical predictions, has enabled an explicit dialogue between theory and experiment that holds the promise of covering this genomic Achilles' heel. The goal is to reach a predictive understanding of transcriptional regulation that makes it possible to calculate gene expression levels from DNA regulatory sequence. This review focuses on the canonical simple repression motif to ask how well the models that have been used to characterize it actually work. We consider a hierarchy of increasingly sophisticated experiments in which the minimal parameter set learned at one level is applied to make quantitative predictions at the next. We show that these careful quantitative dissections provide a template for a predictive understanding of the many more complex regulatory arrangements found across all domains of life.

Indexed as

Gene ExpressionGene Expression RegulationAlgorithmsBinding SitesDNAGenomeDNAallosterybiophysicsgene regulationsimple repressiontranscription

Identifiers

PMID31084583
PMCPMC7001876

What OpenQuestion holds

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Read underepoch 390

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.