Literature DB >> 30715382

Genome-wide association study identifies QTLs for displacement of abomasum in Chinese Holstein cattle1.

Hetian Huang1, Jie Cao2, Gang Guo3, Xizhi Li3, Yachun Wang1, Ying Yu1, Shengli Zhang1, Qin Zhang1, Yi Zhang1.   

Abstract

Displacement of abomasum (DA) is one of the most common and important disorders in dairy cattle. The objective of the present study was to detect the quantitative trait loci (QTL) for DA in Chinese Holstein using single-step genomic BLUP methodology. A total of 60,556 producer-recorded DA event records from 32,190 cows, together with 2,336 genotyped animals with 40,054 SNP markers, were used for the analysis. Genomic data were incorporated into a threshold model for variance component estimation, and the estimated heritability of DA was 0.108 (SE = 0.086). Results of genome-wide association studies were reported as the proportion of genetic variance explained 20-SNP windows. Eight QTLs covering 129 genes on Bos taurus autosomes 2, 4, 7, 10, 14, 17, 20 showed associations with DA. Ten genes, namely BMP4, SOCS4, GCH1, DDHD1, ATG14, ACBP/DBI, SMO, AHCYL2, CYP7A1, and CACNA1A, involved in insulin metabolism and lipid metabolism pathways may be considered as candidate genes of DA in dairy. The identified QTLs, biological pathways, and associated genes underlying DA identified from the present study will contribute to the understanding of the genetic architecture of this complex disease.
© The Author(s) 2019. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  dairy cattle; displacement of abomasum; metabolism pathway; producer-recorded data; quantitative trait loci (QTL); single-step genomic BLUP approach

Mesh:

Year:  2019        PMID: 30715382      PMCID: PMC6396242          DOI: 10.1093/jas/skz031

Source DB:  PubMed          Journal:  J Anim Sci        ISSN: 0021-8812            Impact factor:   3.159


  66 in total

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Authors:  T Geishauser; K Leslie; T Duffield
Journal:  Vet Clin North Am Food Anim Pract       Date:  2000-07       Impact factor: 3.357

2.  PLINK: a tool set for whole-genome association and population-based linkage analyses.

Authors:  Shaun Purcell; Benjamin Neale; Kathe Todd-Brown; Lori Thomas; Manuel A R Ferreira; David Bender; Julian Maller; Pamela Sklar; Paul I W de Bakker; Mark J Daly; Pak C Sham
Journal:  Am J Hum Genet       Date:  2007-07-25       Impact factor: 11.025

3.  Metabolic predictors of displaced abomasum in dairy cattle.

Authors:  S J LeBlanc; K E Leslie; T F Duffield
Journal:  J Dairy Sci       Date:  2005-01       Impact factor: 4.034

4.  Risk factors for abomasal displacement in dairy cows.

Authors:  B W Rohrbach; A L Cannedy; K Freeman; B D Slenning
Journal:  J Am Vet Med Assoc       Date:  1999-06-01       Impact factor: 1.936

5.  Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations.

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Journal:  Mol Nutr Food Res       Date:  2007-02       Impact factor: 5.914

6.  Insulin resistance and abomasal motility disorders in cows detected by use of abomasoduodenal electromyography after surgical correction of left displaced abomasum.

Authors:  Davide Pravettoni; Klaus Doll; Markus Hummel; Elena Cavallone; Michela Re; Angelo G Belloli
Journal:  Am J Vet Res       Date:  2004-10       Impact factor: 1.156

7.  BMP4-BMPR1A signaling in beta cells is required for and augments glucose-stimulated insulin secretion.

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Authors:  P D Constable; G Y Miller; G F Hoffsis; B L Hull; D M Rings
Journal:  Am J Vet Res       Date:  1992-07       Impact factor: 1.156

9.  Effect of medium- and long-chain fatty acid diets on PPAR and SREBP-1 expression and glucose homeostasis in ACBP-overexpressing transgenic rats.

Authors:  S Oikari; T Ahtialansaari; A Huotari; K Kiehne; U R Fölsch; S Wolffram; J Jänne; L Alhonen; K-H Herzig
Journal:  Acta Physiol (Oxf)       Date:  2008-04-03       Impact factor: 6.311

10.  Suppressor of cytokine signaling 1 (SOCS-1) and SOCS-3 cause insulin resistance through inhibition of tyrosine phosphorylation of insulin receptor substrate proteins by discrete mechanisms.

Authors:  Kohjiro Ueki; Tatsuya Kondo; C Ronald Kahn
Journal:  Mol Cell Biol       Date:  2004-06       Impact factor: 4.272

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