Evidence map›Paper›PMID 38346074›Full record

ArticlePLoS computational biology2024

Differential allelic representation (DAR) identifies candidate eQTLs and improves transcriptome analysis.

Lachlan Baer, Karissa Barthelson, John H Postlethwait, David L Adelson, Stephen M Pederson, Michael Lardelli

Open access · goldAbstract read
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Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 47% of its field
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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Lachlan BaerSchool of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0001-5213-3401
Karissa BarthelsonSchool of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0002-4693-8833
John H PostlethwaitInstitute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.ORCID 0000-0002-5476-2137
David L AdelsonSchool of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0003-2404-5636
Stephen M PedersonBlack Ochre Data Labs, Indigenous Genomics, Telethon Kids Institute, Adelaide, South Australia, Australia.ORCID 0000-0001-8197-3303
Michael LardelliSchool of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0002-4289-444X
The University of Adelaide · AUAustralian National University · AUFlinders University · AUUniversity of Oregon · US

Funding

Integrative translational discovery of vascular risk factors in aging and dementiaRF1AG051504 · NIA · MAYO CLINIC JACKSONVILLE · PI BU, GUOJUN, ERTEKIN-TANER, NILUFER · 2015 to 2019
$9.8M
TRANSGENIC MOUSE COREP01AG030128 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WEEBER, EDWIN JOHN · 2009 to 2013
$9.4M
Mechanisms of Sex Determination in ZebrafishR35GM139635 · NIGMS · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2021 to 2025
$1.9M
NIA NIH HHS P01 AG030128NIA NIH HHS RF1 AG051504NIGMS NIH HHS R35 GM139635
6 · The paper itself

Abstract

In comparisons between mutant and wild-type genotypes, transcriptome analysis can reveal the direct impacts of a mutation, together with the homeostatic responses of the biological system. Recent studies have highlighted that, when the effects of homozygosity for recessive mutations are studied in non-isogenic backgrounds, genes located proximal to the mutation on the same chromosome often appear over-represented among those genes identified as differentially expressed (DE). One hypothesis suggests that DE genes chromosomally linked to a mutation may not reflect functional responses to the mutation but, instead, result from an unequal distribution of expression quantitative trait loci (eQTLs) between sample groups of mutant or wild-type genotypes. This is problematic because eQTL expression differences are difficult to distinguish from genes that are DE due to functional responses to a mutation. Here we show that chromosomally co-located differentially expressed genes (CC-DEGs) are also observed in analyses of dominant mutations in heterozygotes. We define a method and a metric to quantify, in RNA-sequencing data, localised differential allelic representation (DAR) between those sample groups subjected to differential expression analysis. We show how the DAR metric can predict regions prone to eQTL-driven differential expression, and how it can improve functional enrichment analyses through gene exclusion or weighting-based approaches. Advantageously, this improved ability to identify probable eQTLs also reveals examples of CC-DEGs that are likely to be functionally related to a mutant phenotype. This supports a long-standing prediction that selection for advantageous linkage disequilibrium influences chromosome evolution. By comparing the genomes of zebrafish (Danio rerio) and medaka (Oryzias latipes), a teleost with a conserved ancestral karyotype, we find possible examples of chromosomal aggregation of CC-DEGs during evolution of the zebrafish lineage. Our method for DAR analysis requires only RNA-sequencing data, facilitating its application across new and existing datasets.

Indexed as

Quantitative Trait LociZebrafishAnimalsGene Expression ProfilingGenotypeRNATranscriptomeRNA

Identifiers

PMID38346074
PMCPMC10890730
OpenAlexW4391743363

What OpenQuestion holds

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LicenceCC BY
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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.