Evidence map›Paper›PMID 20031574›Full record

ArticleCirculation. Cardiovascular genetics2009

Genome-wide identification of allelic expression in hypertensive rats.

Renata I Dmitrieva, Cruz A Hinojos, Megan L Grove, Rebecca J Bell, Eric Boerwinkle, Myriam Fornage, Peter A Doris

Open access · bronzeAbstract read
In one paragraph

Article in Circulation. Cardiovascular genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Renata I DmitrievaInstitute of Molecular Medicine and Human Genetics Center, University of Texas Health Science Center, 2121 Holcombe Blvd., Houston, TX 77030, USA.
Cruz A Hinojos
Megan L Grove
Rebecca J Bell
Eric Boerwinkle
Myriam Fornage
Peter A Doris
The University of Texas Health Science Center at Houston · US

Funding

MOLECULAR EPIDEMIOLOGY OF ESSENTIAL HYPERTENSIONR37HL051021 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BOERWINKLE, ERIC A. · 1999 to 2008
$10.8M
FUNCTIONAL GENOMICS OF ARTERIAL THROMBOSISR01NS041466 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FORNAGE, MYRIAM · 2000 to 2004
$1.9M
Gene-Environment Interactions and Stroke SusceptibilityR01HL069126 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FORNAGE, MYRIAM · 2001 to 2004
$1.7M
HNF1 transcriptional control of renal oxidative stressR01DK069632 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DORIS, PETER A · 2005 to 2009
$1.4M
CARDIOTONIC STEROIDS FROM THE ADRENAL GLANDR01DK045538 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DORIS, PETER A · 1994 to 2002
$697k
MOLECULAR EPIDEMIOLOGY OF ESSENTIAL HYPERTENSIONR01HL051021 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BOERWINKLE, ERIC A · 1994 to 1998
–
NHLBI NIH HHS HL51021NHLBI NIH HHS HL69126NHLBI NIH HHS R01 HL069126NHLBI NIH HHS R37 HL051021NIDDK NIH HHS R01 DK045538NIDDK NIH HHS R01 DK069632NINDS NIH HHS NS41466NINDS NIH HHS R01 NS041466PHS HHS DDK45538PHS HHS DDK74680
6 · The paper itself

Abstract

backgroundIdentification of genes involved in complex cardiovascular disease traits has proven challenging. Inbred animal models can facilitate genetic studies of disease traits. The spontaneously hypertensive rat (SHR) is an inbred model of hypertension that exists in several closely related but genetically distinct lines. METHODS AND

resultsWe used renal gene-expression profiling across 3 distinct SHR lines to identify genes that show different expression in SHR than in the genetically related normotensive control strain, Wistar-Kyoto. To ensure robust discovery of genes showing SHR-specific expression differences, we considered only those genes in which differential expression is replicated in multiple animals of each of multiple hypertensive rat lines at multiple time points during the ontogeny of hypertension. Mutation analysis was performed on the identified genes to uncover allelic variation. We identified those genes in which all SHR lines share a single allele of the gene when normotensive controls (Wistar-Kyoto) have fixed the alternative allele. We then identified which of the differentially expressed genes show expression that is controlled by the alleleic variation present in and around the gene. Allelic expression was demonstrated by observing the effect on gene expression of alleles inherited in the freely segregating F(2) progeny of a cross between SHR and Wistar-Kyoto animals.

conclusionsThe result of these studies is the identification of several genes (Ptprj, Ela1, Dapk-2, and Gstt2) in which each of 4 SHR lines examined have fixed the same allele and in which each of 2 Wistar-Kyoto lines have a contrasting allele for which the inherited allele influences the level of gene expression. We further show that alleles of these genes lie in extensive haplotype blocks that have been inherited identical by descent in the hypertensive lines.

Indexed as

Genome-Wide Association StudyAllelesAnimalsBlood PressureDisease Models, AnimalFemaleGene Expression ProfilingHumansHypertensionKidneyMalePedigreePolymorphism, Single NucleotideRatsRats, Inbred SHRRats, Inbred WKY

Identifiers

PMID20031574
PMCPMC2760851
OpenAlexW2047536612

What OpenQuestion holds

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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.