Evidence map›Paper›PMID 24825890›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Interactions between chromosomal and nonchromosomal elements reveal missing heritability.

Matthew D Edwards, Anna Symbor-Nagrabska, Lindsey Dollard, David K Gifford, Gerald R Fink

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
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  9. Loss-of-function mutation survey revealed that genes with background-dependent fitness are rare and functionally related in yeast.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Adaptive Response ofJournal of fungi (Basel, Switzerland) · 2022
    Article
  11. Review
  12. Article
  13. Review
  14. Complex modifier landscape underlying genetic background effects.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. Review
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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

5 authors.

Matthew D EdwardsComputer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02139;
Anna Symbor-NagrabskaWhitehead Institute for Biomedical Research, Cambridge, MA 02142;
Lindsey DollardWhitehead Institute for Biomedical Research, Cambridge, MA 02142;
David K GiffordComputer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02139;Whitehead Institute for Biomedical Research, Cambridge, MA 02142;Broad Institute of MIT and Harvard University, Cambridge, MA 02142; andDepartment of Stem Cell and Regenerative Biology, Harvard University and Harvard Medical School, Cambridge, MA 02138 gifford@mit.edu gfink@wi.mit.edu.
Gerald R FinkWhitehead Institute for Biomedical Research, Cambridge, MA 02142;Broad Institute of MIT and Harvard University, Cambridge, MA 02142; and gifford@mit.edu gfink@wi.mit.edu.

Funding

REGULATION OF HISTIDINE BIOSYNTHESIS IN YEASTR01GM035010 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI FINK, GERALD R · 1985 to 2016
$9.9M
REGULATION OF HISTIDINE BIOSYNTHESIS IN YEASTR37GM035010 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI FINK, GERALD R · 1986 to 1995
–
NIGMS NIH HHS GM035010NIGMS NIH HHS R01 GM035010
6 · The paper itself

Abstract

The measurement of any nonchromosomal genetic contribution to the heritability of a trait is often confounded by the inability to control both the chromosomal and nonchromosomal information in a population. We have designed a unique system in yeast where we can control both sources of information so that the phenotype of a single chromosomal polymorphism can be measured in the presence of different cytoplasmic elements. With this system, we have shown that both the source of the mitochondrial genome and the presence or absence of a dsRNA virus influence the phenotype of chromosomal variants that affect the growth of yeast. Moreover, by considering this nonchromosomal information that is passed from parent to offspring and by allowing chromosomal and nonchromosomal information to exhibit nonadditive interactions, we are able to account for much of the heritability of growth traits. Taken together, our results highlight the importance of including all sources of heritable information in genetic studies and suggest a possible avenue of attack for finding additional missing heritability.

Indexed as

Models, GeneticPhenotypeAnalysis of VarianceChromosomesComputational BiologyExtrachromosomal InheritanceGene FrequencyGenetic TherapyHumansMitochondrial DiseasesPolymorphism, Single NucleotideYeastsextrachromosomalgenetic interactionsnonlinear model

Identifiers

PMID24825890
PMCPMC4040555

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.