Evidence map›Paper›PMID 28872114›Full record

ArticleJournal of visualized experiments : JoVE2017

Quantification of Information Encoded by Gene Expression Levels During Lifespan Modulation Under Broad-range Dietary Restriction in C. elegans.

Dhaval S Patel, Giovanni Diana, Eugeni V Entchev, Mei Zhan, Hang Lu, QueeLim Ch'ng

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Dhaval S PatelCentre for Developmental Neurobiology, King's College London.
Giovanni DianaCentre for Developmental Neurobiology, King's College London.
Eugeni V EntchevCentre for Developmental Neurobiology, King's College London.
Mei ZhanInterdisciplinary Bioengineering Graduate Program, Georgia Institute of Technology; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology; School of Chemical & Biomolecular Engineering, Georgia Institute of Technology.
Hang LuInterdisciplinary Bioengineering Graduate Program, Georgia Institute of Technology; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology; School of Chemical & Biomolecular Engineering, Georgia Institute of Technology.
QueeLim Ch'ngCentre for Developmental Neurobiology, King's College London; queelim@kcl.ac.uk.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Quantitative microscopy-based rapid phenotyping and screeningR01GM088333 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2011 to 2018
$2.3M
Sources, transmission and effects of transcriptional noise in C. elegans agingR01AG035317 · NIA · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2009 to 2011
$837k
Biotechnology and Biological Sciences Research Council BB/H020500/1Biotechnology and Biological Sciences Research Council BB/M00757X/1European Research Council 242666NIA NIH HHS R01 AG035317NIGMS NIH HHS R01 GM088333NIH HHS P40 OD010440Wellcome TrustWellcome Trust 087146
6 · The paper itself

Abstract

Sensory systems allow animals to detect, process, and respond to their environment. Food abundance is an environmental cue that has profound effects on animal physiology and behavior. Recently, we showed that modulation of longevity in the nematode Caenorhabditis elegans by food abundance is more complex than previously recognized. The responsiveness of the lifespan to changes in food level is determined by specific genes that act by controlling information processing within a neural circuit. Our framework combines genetic analysis, high-throughput quantitative imaging and information theory. Here, we describe how these techniques can be used to characterize any gene that has a physiological relevance to broad-range dietary restriction. Specifically, this workflow is designed to reveal how a gene of interest regulates lifespan under broad-range dietary restriction; then to establish how the expression of the gene varies with food level; and finally, to provide an unbiased quantification of the amount of information conveyed by gene expression about food abundance in the environment. When several genes are examined simultaneously under the context of a neural circuit, this workflow can uncover the coding strategy employed by the circuit.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCaloric RestrictionGene ExpressionLongevityCaenorhabditis elegans Proteins

Identifiers

PMID28872114
PMCPMC5614333

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.