Evidence map›Paper›PMID 23422947›Full record

ArticleScientific reports2013

Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines.

Jubao Duan, Jianxin Shi, Xijin Ge, Lars Dölken, Winton Moy, Deli He, Sandra Shi, Alan R Sanders, Jeff Ross, Pablo V Gejman

Abstract read
In one paragraph

Article in Scientific reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
–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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Characterization ofSynthetic and systems biotechnology · 2027
    Article
  4. The Kinetic Intron Hypothesis.bioRxiv : the preprint server for biology · 2026
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  20. Decoding the effects of synonymous variants.Nucleic acids research · 2021
    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

10 authors.

Jubao DuanCenter for Psychiatric Genetics, NorthShore University HealthSystem Research Institute. Evanston, Illinois 60201, USA. jduan@uchicago.edu
Jianxin Shi
Xijin Ge
Lars Dölken
Winton Moy
Deli He
Sandra Shi
Alan R Sanders
Jeff Ross
Pablo V Gejman

Funding

1/2 An Integrative Genetic Investigation of SchizophreniaR01MH094091 · NIMH · ENDEAVOR HEALTH CLINICAL OPERATIONS · PI GEJMAN, PABLO V. · 2011 to 2015
$2.7M
Joint Mapping of Genome-Wide Gene Expression and Association in a Schizophrenia DRC2MH090030 · NIMH · ENDEAVOR HEALTH CLINICAL OPERATIONS · PI SANDERS, ALAN R · 2009 to 2010
$2.0M
Medical Research Council G1002523NIMH NIH HHS R01 MH094091NIMH NIH HHS R01MH94091NIMH NIH HHS RC2 MH090030NIMH NIH HHS RC2MH090030
6 · The paper itself

Abstract

The extent to which RNA stability differs between individuals and its contribution to the interindividual expression variation remain unknown. We conducted a genome-wide analysis of RNA stability in seven human HapMap lymphoblastoid cell lines (LCLs) and analyzed the effect of DNA sequence variation on RNA half-life differences. Twenty-six percent of the expressed genes exhibited RNA half-life differences between LCLs at a false discovery rate (FDR) < 0.05, which accounted for ~ 37% of the gene expression differences between individuals. Nonsense polymorphisms were associated with reduced RNA half-lives. In genes presenting interindividual RNA half-life differences, higher coding GC3 contents (G and C percentages at the third-codon positions) were correlated with increased RNA half-life. Consistently, G and C alleles of single nucleotide polymorphisms (SNPs) in protein coding sequences were associated with enhanced RNA stability. These results suggest widespread interindividual differences in RNA stability related to DNA sequence and composition variation.

Indexed as

Genome, HumanAdultAllelesAnalysis of VarianceBase CompositionBase SequenceCodon, NonsenseComputational BiologyFemaleGenetic VariationGenotypeHalf-LifeHapMap ProjectHumansMaleMiddle AgedCodon, NonsenseRNA

Identifiers

PMID23422947
PMCPMC3576867

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Registered trials

None linked

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.