Evidence map›Paper›PMID 25099818›Full record

ArticleBiophysical journal2014

Simple biochemical pathways far from steady state can provide switchlike and integrated responses.

Stefano Di Talia, Eric F Wieschaus

Abstract read
In one paragraph

Article in Biophysical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Measuring time during early embryonic development.Seminars in cell & developmental biology · 2016
    Review
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

2 authors.

Stefano Di TaliaDepartment of Cell Biology, Duke University Medical Center, Durham, North Carolina. Electronic address: stefano.ditalia@duke.edu.
Eric F WieschausHoward Hughes Medical Institute, Department of Molecular Biology, Princeton University, Princeton, New Jersey.

Funding

OOGENESIS AND EARLY EMBRYOGENESIS IN DROSOPHILAR37HD015587 · NICHD · PRINCETON UNIVERSITY · PI WIESCHAUS, ERIC F. · 1989 to 2015
$1.9M
Time-keeping Mechanisms in Drosophila Embryonic DevelopmentR00HD074670 · NICHD · DUKE UNIVERSITY · PI DI TALIA, STEFANO · 2014 to 2016
$705k
Time-keeping mechanisms in Drosophila embryonic developmentK99HD074670 · NICHD · PRINCETON UNIVERSITY · PI DI TALIA, STEFANO · 2013 to 2013
$97k
Howard Hughes Medical InstituteNICHD NIH HHS 1K99HD074670NICHD NIH HHS 5R37HD15587NICHD NIH HHS K99 HD074670NICHD NIH HHS R00 HD074670NICHD NIH HHS R37 HD015587
6 · The paper itself

Abstract

Covalent modification cycles (systems in which the activity of a substrate is regulated by the action of two opposing enzymes) and ligand/receptor interactions are ubiquitous in signaling systems and their steady-state properties are well understood. However, the behavior of such systems far from steady state remains unclear. Here, we analyze the properties of covalent modification cycles and ligand/receptor interactions driven by the accumulation of the activating enzyme and the ligand, respectively. We show that for a large range of parameters both systems produce sharp switchlike response and yet allow for temporal integration of the signal, two desirable signaling properties. Ultrasensitivity is observed also in a region of parameters where the steady-state response is hyperbolic. The temporal integration properties are tunable by regulating the levels of the deactivating enzyme and receptor, as well as by adjusting the rate of accumulation of the activating enzyme and ligand. We propose that this tunability is used to generate precise responses in signaling systems.

Indexed as

Models, BiologicalProtein Processing, Post-TranslationalSignal TransductionEnzymesKineticsReceptors, Cell SurfaceEnzymesReceptors, Cell Surface

Identifiers

PMID25099818
PMCPMC4129562

What OpenQuestion holds

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Registered trials

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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.