Evidence map›Paper›PMID 24165562›Full record

ArticleBMC genetics2013

Body composition and gene expression QTL mapping in mice reveals imprinting and interaction effects.

Ye Cheng, Satyanarayana Rachagani, Angela Cánovas, Mary Sue Mayes, Richard G Tait, Jack C M Dekkers, James M Reecy

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Article in BMC genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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4 citing papers in PubMed.

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  4. Endocrine crosstalk between muscle and bone.Current osteoporosis reports · 2014
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5 · Who and what money

Authors and funding

7 authors.

Ye Cheng
Satyanarayana Rachagani
Angela Cánovas
Mary Sue Mayes
Richard G Tait
Jack C M Dekkers
James M ReecyDepartment of Animal Science, Iowa State University, 2255 Kildee, Ames, IA, USA. jreecy@iastate.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundShifts in body composition, such as accumulation of body fat, can be a symptom of many chronic human diseases; hence, efforts have been made to investigate the genetic mechanisms that underlie body composition. For example, a few quantitative trait loci (QTL) have been discovered using genome-wide association studies, which will eventually lead to the discovery of causal mutations that are associated with tissue traits. Although some body composition QTL have been identified in mice, limited research has been focused on the imprinting and interaction effects that are involved in these traits. Previously, we found that Myostatin genotype, reciprocal cross, and sex interacted with numerous chromosomal regions to affect growth traits.

resultsHere, we report on the identification of muscle, adipose, and morphometric phenotypic QTL (pQTL), translation and transcription QTL (tQTL) and expression QTL (eQTL) by applying a QTL model with additive, dominance, imprinting, and interaction effects. Using an F2 population of 1000 mice derived from the Myostatin-null C57BL/6 and M16i mouse lines, six imprinted pQTL were discovered on chromosomes 6, 9, 10, 11, and 18. We also identified two IGF1 and two Atp2a2 eQTL, which could be important trans-regulatory elements. pQTL, tQTL and eQTL that interacted with Myostatin, reciprocal cross, and sex were detected as well. Combining with the additive and dominance effect, these variants accounted for a large amount of phenotypic variation in this study.

conclusionsOur study indicates that both imprinting and interaction effects are important components of the genetic model of body composition traits. Furthermore, the integration of eQTL and traditional QTL mapping may help to explain more phenotypic variation than either alone, thereby uncovering more molecular details of how tissue traits are regulated.

Indexed as

Chromosome MappingGenomic ImprintingQuantitative Trait LociAdiposityAnimalsBody CompositionChromosomesFemaleGenetic VariationGenotypeInsulin-Like Growth Factor IMaleMiceMice, Inbred C57BLMyostatinPhenotypeAtp2a2 protein, mouseinsulin-like growth factor-1, mouseInsulin-Like Growth Factor IMyostatinSarcoplasmic Reticulum Calcium-Transporting ATPases

Identifiers

PMID24165562
PMCPMC4233306

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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.