Evidence map›Paper›PMID 25613955›Full record

ArticleBMC genomics2015

Overlapping mouse subcongenic strains successfully separate two linked body fat QTL on distal MMU 2.

Rodrigo Gularte-Mérida, Charles R Farber, Ricardo A Verdugo, Alma Islas-Trejo, Thomas R Famula, Craig H Warden, Juan F Medrano

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

5 citing papers in PubMed, 19 citations in OpenAlex.

  1. Burly1 is a mouse QTL for lean body mass that maps to a 0.8-Mb region of chromosome 2.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
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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 5 institutions in 3 countries.

Rodrigo Gularte-MéridaDepartment of Animal Science, University of California, Davis, CA, 95616-8521, USA. rodrigo.gularte@ulg.ac.be.
Charles R FarberCenter for Public Health Genomics, University of Virginia, Charlottesville, VA, 22908, USA. crf2s@virginia.edu.
Ricardo A VerdugoDepartment of Animal Science, University of California, Davis, CA, 95616-8521, USA. ricardo.a.verdugo@gmail.com.
Alma Islas-TrejoDepartment of Animal Science, University of California, Davis, CA, 95616-8521, USA. adislas@ucdavis.edu.
Thomas R FamulaDepartment of Animal Science, University of California, Davis, CA, 95616-8521, USA. trfamula@ucdavis.edu.
Craig H WardenRowe Genetics Program and Department of Pediatrics, University of California, Davis, CA, 95616-8521, USA. chwarden@ucdavis.edu.
Juan F MedranoDepartment of Animal Science, University of California, Davis, CA, 95616-8521, USA. jfmedrano@ucdavis.edu.
University of California, Davis · USAnimal Welfare Institute · USUniversity of California System · USUniversity of Liège · BEUniversity of Virginia Health System · US

Funding

Positional cloning of obesity genes from congenic miceR01DK069978 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI WARDEN, CRAIG H · 2006 to 2010
$1.7M
NIDDK NIH HHS DK69978NIDDK NIH HHS R01 DK069978
6 · The paper itself

Abstract

backgroundMouse chromosome 2 is linked to growth and body fat phenotypes in many mouse crosses. With the goal to identify the underlying genes regulating growth and body fat on mouse chromosome 2, we developed five overlapping subcongenic strains that contained CAST/EiJ donor regions in a C57BL/6J (hg/hg) background (hg is a spontaneous deletion of 500 Kb on mouse chromosome 10). To fine map QTL on distal mouse chromosome 2 a total of 1,712 F2 mice from the five subcongenic strains, plus 278 F2 mice from the HG2D founder congenic strain were phenotyped and analyzed. Interval mapping (IM) and composite IM (CIM) were performed on body weight and body fat traits on a combination of SNP and microsatellite markers, which generated a high-density genotyping panel.

resultsPhenotypic analysis and interval mapping of total fat mass identified two QTL on distal mouse chromosome 2. One QTL between 150 and 161 Mb, Fatq2a, and the second between 173.3 and 175.6 Mb, Fatq2b. The two QTL reside in different congenic strains with significant total fat differences between homozygous cast/cast and b6/b6 littermates. Both of these QTL were previously identified only as a single QTL affecting body fat, Fatq2. Furthermore, through a novel approach referred here as replicated CIM, Fatq2b was mapped to the Gnas imprinted locus.

conclusionsThe integration of subcongenic strains, high-density genotyping, and CIM succesfully partitioned two previously linked QTL 20 Mb apart, and the strongest QTL, Fatq2b, was fine mapped to a ~2.3 Mb region interval encompassing the Gnas imprinted locus.

Indexed as

Quantitative Trait LociAdipose TissueAnimalsBinding SitesBody WeightBrainChromosome MappingChromosomesFemaleGenetic LinkageGenotypeMaleMiceMice, Inbred C57BLMicroRNAsPhenotypeMicroRNAsTranscription Factors

Identifiers

PMID25613955
PMCPMC4308015
OpenAlexW2091235919

What OpenQuestion holds

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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.