Evidence map›Paper›PMID 19818800›Full record

ArticleTheoretical population biology2010

Epistasis in a quantitative trait captured by a molecular model of transcription factor interactions.

Jason Gertz, Justin P Gerke, Barak A Cohen

Abstract read
In one paragraph

Article in Theoretical population biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Cis-regulatory elements and human evolution.Current opinion in genetics & development · 2014
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
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  20. 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

3 authors.

Jason GertzCenter for Genome Sciences, Department of Genetics, Washington University in St. Louis School of Medicine, 4444 Forest Park Blvd., St. Louis, MO 63108, United States.
Justin P Gerke
Barak A Cohen

Funding

Deciphering the regulatory code of a cellR01GM078222 · NIGMS · WASHINGTON UNIVERSITY · PI STORMO, GARY D · 2007 to 2010
$1.8M
NIGMS NIH HHS GM078222-01A1NIGMS NIH HHS R01 GM078222
6 · The paper itself

Abstract

With technological advances in genetic mapping studies more of the genes and polymorphisms that underlie Quantitative Trait Loci (QTL) are now being identified. As the identities of these genes become known there is a growing need for an analysis framework that incorporates the molecular interactions affected by natural polymorphisms. As a step towards such a framework we present a molecular model of genetic variation in sporulation efficiency between natural isolates of the yeast, Saccharomyces cerevisiae. The model is based on the structure of the regulatory pathway that controls sporulation. The model captures the phenotypic variation between strains carrying different combinations of alleles at known QTL. Compared to a standard linear model the molecular model requires fewer free parameters, and has the advantage of generating quantitative hypotheses about the affinity of specific molecular interactions in different genetic backgrounds. Our analyses provide a concrete example of how the thermodynamic properties of protein-protein and protein-DNA interactions naturally give rise to epistasis, the non-linear relationship between genotype and phenotype. As more causative genes and polymorphisms underlying QTL are identified, thermodynamic analyses of quantitative traits may provide a useful framework for unraveling the complex relationship between genotype and phenotype.

Indexed as

Epistasis, GeneticModels, GeneticGenetic VariationGenotypeHumansNonlinear DynamicsPhenotypePolymorphism, GeneticQuantitative Trait LociSaccharomyces cerevisiaeSpores, FungalThermodynamicsTranscription FactorsTranscription Factors

Identifiers

PMID19818800
PMCPMC2813966

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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.