Evidence map›Paper›PMID 19671657›Full record

ArticlePhysiological genomics2009

Effects of atherogenic diet on hepatic gene expression across mouse strains.

Keith R Shockley, David Witmer, Sarah L Burgess-Herbert, Beverly Paigen, Gary A Churchill

Abstract read
In one paragraph

Article in Physiological genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% 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

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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Macronutrient modulation of mRNA and microRNA function in animals: A review.Animal nutrition (Zhongguo xu mu shou yi xue hui) · 2020
    Review
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  12. Single subject transcriptome analysis to identify functionally signed gene set or pathway activity.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2018
    Article
  13. Article
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  15. Article
  16. Article
  17. Modeling progressive non-alcoholic fatty liver disease in the laboratory mouse.Mammalian genome : official journal of the International Mammalian Genome Society · 2014
    Review
  18. Article
  19. Article
  20. In vitro and in vivo models of non-alcoholic fatty liver disease (NAFLD).International journal of molecular sciences · 2013
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Keith R ShockleyThe Jackson Laboratory, Bar Harbor, Maine 04605, USA. shockleykr@niehs.nih.gov
David Witmer
Sarah L Burgess-Herbert
Beverly Paigen
Gary A Churchill
Jackson Laboratory · USMaine School of Science and Mathematics · US

Funding

UNC and PERLEGEN, IncP50GM076468 · NIGMS · JACKSON LABORATORY · PI CHURCHILL, GARY A · 2006 to 2015
$31.0M
From QTL to Gene for HDL CholesterolR37HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2009 to 2018
$4.3M
From QTL to Gene for HDL CholesterolR01HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2004 to 2008
$2.1M
Identifying Genes Regulating HDL Cholesterol LevelsR01HL074086 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2004 to 2007
$994k
ANOVA-Based Approaches to Time-Series Microarray DataF32HG003968 · NHGRI · JACKSON LABORATORY · PI SHOCKLEY, KEITH R · 2005 to 2007
$142k
Howard Hughes Medical InstituteNHGRI NIH HHS HG-003968NHLBI NIH HHS HL-74086NHLBI NIH HHS HL-77796NIGMS NIH HHS GM-076468
6 · The paper itself

Abstract

Diets high in fat and cholesterol are associated with increased obesity and metabolic disease in mice and humans. To study the molecular basis of the metabolic response to dietary fat, 10 inbred strains of mice were fed atherogenic high-fat and control low-fat diets. Liver gene expression and whole animal phenotypes were measured and analyzed in both sexes. The effects of diet, strain, and sex on gene expression were determined irrespective of complex processes, such as feedback mechanisms, that could have mediated the genomic responses. Global gene expression analyses demonstrated that animals of the same strain and sex have similar transcriptional profiles on a low-fat diet, but strains may show considerable variability in response to high-fat diet. Functional profiling indicated that high-fat feeding induced genes in the immune response, indicating liver damage, and repressed cholesterol biosynthesis. The physiological significance of the transcriptional changes was confirmed by a correlation analysis of transcript levels with whole animal phenotypes. The results found here were used to confirm a previously identified quantitative trait locus on chromosome 17 identified in males fed a high-fat diet in two crosses, PERA x DBA/2 and PERA x I/Ln. The gene expression data and phenotype data have been made publicly available as an online tool for exploring the effects of atherogenic diet in inbred mouse strains (http://cgd-array.jax.org/DietStrainSurvey).

Indexed as

Diet, AtherogenicAnalysis of VarianceAnimalsCluster AnalysisFemaleGene Expression ProfilingLiverMaleMiceMice, Inbred BALB CMice, Inbred C3HMice, Inbred C57BLMice, Inbred DBAMice, Inbred StrainsOligonucleotide Array Sequence AnalysisSpecies Specificity

Identifiers

PMID19671657
PMCPMC2789673
OpenAlexW2141674000

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.